Inhalt des Dokuments
Publications
- 2021
- 2020
- 2019
- 2018
- 2017
- 2016
- 2015
- 2014
- 2013
- 2012
- 2011
- 2010
- 2009
- 2008
- 2007
- 2006
- 2005
- 2004
- 2003
- 1999
- Publications with Professor Larry E. Overman
- Publications with Professor Dieter Hoppe
- Publications with Professor Paul Knochel
312.
Y. Xu, H. Yi, and
M. Oestreich,
Enantio- and Regioconvergent Synthesis of
Allenylsilanes by Nickel-Catalyzed
C(sp2)–C(sp3) Cross-Coupling Starting from
Racemic α-Silylated Propargylic Bromides,
submitted for
publication.
311.
N. Kranidiotis-Hisatomi, H. Yi, and M. Oestreich,
Enantio-
and Regioconvergent Nickel-Catalyzed
C(sp3)–C(sp3) Cross-Coupling of Allylic
Electrophiles Steered by a Silyl Group,
submitted for
publication.
310.
S. C. Richter and M. Oestreich,
Chemoselective
Deoxygenation of 2° Benzylic Alcohols through a Sequence of
Formylation and B(C6F5)3-Catalyzed
Reduction,
Eur. J. Org. Chem. in revision.
309.
B. M. Gross and M.
Oestreich,
The Trityl Cation Embedded into a
[7]Helicene-Like Backbone: Preparation and Application as a Lewis Acid
Catalyst,
Synthesis 2021,
53, Accepted Manuscript on March 3, 2021 [1]. (Abstract
[2])
308.
H. Fang, G. Wang, and M. Oestreich,
Mild Reductive
Rearrangement of Oximes and Oxime Ethers to Secondary Amines with
Hydrosilanes Catalyzed by
B(C6F5)3,
submitted for
publication.
307.
E. Romain, K. de la Vega-Hernández, F. Guégan, J. Sanz García, C.
Fopp, F. Chemla, F. Ferreira, H. Gerard, O. Jackowski, S. Halbert, M.
Oestreich, and A. Perez-Luna,
Development of a Radical
Silylzincation of (Het)Aryl-Substituted Alkynes and Computational
Insights into the Origin of the Trans-Stereoselectivity,
Adv. Synth. Catal. in revision.
306.
H. F. T.
Klare, L. Albers, L. Süsse, S.
Keess, T. Müller, and M. Oestreich,
Silylium Ions: From Elusive Reactive Intermediates to Potent
Catalysts (Review),
Chem. Rev.
2021, 121, accepted for publication.
[3]
- © 2021 WILEY-VCH
305.
H. Fang, K. Xie, S.
Kemper, and M. Oestreich,
Consecutive β,β’-Selective
C(sp3)–H Silylation of Tertiary Amines with
Dihydrosilanes Catalyzed by
B(C6F5)3,
Angew. Chem.
Int. Ed. 2021, 60, early view on March
3, 2021 [4]. (Abstract [5])
Selected as a "Hot Paper"
by Angewandte Chemie.
(open access)
[6]
- © 2021 American Chemical Society
304.
L. Zhang and M.
Oestreich,
Diastereotopic Group-Selective Intramolecular
Aldol Reactions Initiated by Enantioselective Conjugate Silylation:
Diastereodivergence Controlled by the Silicon Nucleophile,
ACS Catal. 2021, 11, 3516-3522
[7]. (Abstract [8])
[9]
- © 2021 WILEY-VCH
303.
A. Roy and M.
Oestreich,
At Long Last: The Me3Si Group as a
Masked Alcohol (Highlight),
Angew. Chem.
2021, 133, 4456-4458;
Angew. Chem.
Int. Ed. 2021, 60, 4408-4410 [10].
(Abstract [11]).
[12]
- © 2020 American Chemical Society
302.
Z. Papadopulu and M.
Oestreich,
Kinetic Resolution of Neopentylic Secondary
Alcohols by Cu–H-Catalyzed Enantioselective Silylation with
Hydrosilanes,
Org. Lett. 2021,
23, 438-441 [13]. (Abstract [14])
[15]
- © 2020 Royal Society of Chemistry
301.
J.-J. Feng, W. Mao,
L. Zhang, and M. Oestreich,
Activation of the
Si–B interelement bond related to catalysis (Review),
Chem. Soc. Rev. 2021, 50,
2010-2073 [16]. (Abstract [17])
(open access)
[18]
- © 2020 Royal Society of Chemistry
300.
T. He, G. Wang, P.-W.
Long, S. Kemper, E. Irran, H. F. T. Klare, and M. Oestreich,
Intramolecular Friedel-Crafts alkylation with a
silylium-ion-activated cyclopropyl group: formation of tricyclic ring
systems from benzyl-substituted vinylcyclopropanes and
hydrosilanes,
Chem. Sci. 2021,
12, 569-575 [19]. (Abstract)
Selected for the 2020
Chemical Science HOT Article Collection [20]
(open
access)
[21]
- © 2020 WILEY-VCH
299.
J. Seliger and M.
Oestreich,
Dynamic Kinetic Resolution of Alcohols by
Enantioselective Silylation Enabled by Two Orthogonal Transition-Metal
Catalysts,
Angew. Chem. 2021,
133, 251-255;
Angew. Chem. Int. Ed.
2021, 60, 247-251 [22]. (Abstract [23])
Selected as a "Hot Paper" by Angewandte
Chemie.
(open access)
[24]
- © 2020 American Chemical Society
298.
M. Oberling,
E. Irran, Y. Ohki, H. F. T. Klare, and M.
Oestreich,
Cationic Ru–Se Complexes for Cooperative Si–H
Bond Activation,
Organometallics
2020, 39, 4747-4753 [25]. (Abstract
[26])
[27]
- © 2020 Royal Society of Chemistry
297.
H. Fang and M.
Oestreich,
Defunctionalisation catalysed by boron Lewis
acids (Perspective),
Chem. Sci.
2020, 11, 12604-12615 [28]. (Abstract
[29])
Part of the themed collection Celebrating 10 years of
Chemical Science [30]
(open access)
[31]
- © 2020 American Chemical Society
296.
W. Mao and M.
Oestreich,
Enantioselective Synthesis of α-Chiral
Propargylic Silanes by Copper-Catalyzed 1,4-Selective Addition of
Silicon Nucleophiles to Enyne-Type α,β,γ,δ-Unsaturated
Acceptors,
Org. Lett. 2020,
22, 8096-8100 [32]. (Abstract [33])
[34]
- © 2020 WILEY-VCH
295.
W. Chen, H. Fang, K.
Xie, and M. Oestreich,
The Cyclohexa-2,5-dienyl Group as a
Placeholder for Hydrogen: Organocatalytic Michael Addition of an
Acetaldehyde Surrogate,
Chem. Eur. J.
2020, 26, 15126-15129 [35]. (Abstract
[36])
(open access)
[37]
- © 2020 American Chemical Society
294.
P.-W. Long, T. He, and
M. Oestreich,
B(C6F5)3-Catalyzed
Hydrosilylation of Vinylcyclopropanes,
Org. Lett.
2020, 22, 7383-7386 [38]. (Abstract
[39])
[40]
- © 2020 American Chemical Society
293.
W. Xue and M.
Oestreich,
Beyond Carbon: Enantioselective and
Enantiospecific Reactions with Catalytically Generated Boryl- and
Silylcopper Intermediates (Outlook),
ACS Cent. Sci.
2020, 6, 1070-1081 [41]. (Abstract [42])
ACS AuthorChoice (open access)
[43]
- © 2020 WILEY-VCH
292.
C. Chauvier, L.
Finck, E. Irran, and M. Oestreich,
Autocatalytic Carbonyl
Arylation through In-Situ Release of Aryl Nucleophiles from
N-Aryl-N’-Silyldiazenes,
Angew. Chem.
2020, 132, 12436-12440;
Angew.
Chem. Int. Ed. 2020, 59, 12337-12341
[44]. (Abstract [45])
(open access)
[46]
- © 2020 WILEY-VCH
291.
T. He, G. Wang, V.
Bonetti, H. F. T. Klare, and M. Oestreich,
Silylium-Ion-Promoted (5+1) Cycloaddition of Aryl-Substituted
Vinylcyclopropanes and Hydrosilanes Involving Aryl Migration,
Angew. Chem. 2020, 132,
12284-12289;
Angew. Chem. Int. Ed.
2020, 59, 12186-12191 [47]. (Abstract
[48])
(open access)
[49]
- © 2020 American Chemical Society
290.
M. Cui and M.
Oestreich,
Copper-Catalyzed Enantioselective and
Exo-Selective Addition of Silicon Nucleophiles to 7-Oxa- and
7-Azabenzonorbornadiene Derivatives,
Org. Lett.
2020, 22, 3684-3687 [50]. (Abstract
[51])
[52]
- © 2020 WILEY-VCH
289.
H. Fang and M.
Oestreich,
Reductive Deamination with Hydrosilanes Catalyzed
by B(C6F5)3,
Angew.
Chem. 2020, 132, 11491-11495;
Angew. Chem. Int. Ed. 2020, 59,
11394-11398 [53]. (Abstract [54])
(open access)
Highlighted
in SYNFACTS 2020, 16, 837
[55].
[56]
- © 2020 WILEY-VCH
288.
Q. Wu, A. Roy, G.
Wang, E. Irran, H. F. T. Klare, and M. Oestreich,
Synthesis
of a Counteranion-Stabilized Bis(silylium) Ion,
Angew.
Chem. 2020, 132, 10609-10613;
Angew. Chem. Int. Ed. 2020, 59,
10523-10526 [57]. (Abstract [58])
Highlighted as a
"Very Important Paper (VIP)" by
Angewandte Chemie.
(open access)
[59]
- © 2020 American Chemical Society
287.
A. Roy, V. Bonetti, G.
Wang, Q. Wu, H. F. T. Klare, and M. Oestreich,
Silylium-Ion-Promoted Ring-Opening Hydrosilylation and
Disilylation of Unactivated Cyclopropanes,
Org.
Lett. 2020, 22, 1213-1216 [60].
(Abstract [61])
[62]
- © 2020 WILEY-VCH
286.
D. Janssen-Müller
and M. Oestreich,
Transition-Metal-Like Catalysis with
a Main-Group Element: Bismuth-Catalyzed C-F Coupling of Aryl Boronic
Esters (Highlight),
Angew. Chem.
2020, 132, 8404-8406;
Angew. Chem.
Int. Ed. 2020, 59, 8328-8330 [63].
(Abstract [64])
[65]
- © 2020 American Chemical Society
285.
A.-C. Schulz, S.
Frielingsdorf, P. Pommerening, L. Lauterbach, G. Bistoni, F. Neese, M.
Oestreich, and O. Lenz,
Formyltetrahydrofolate Decarbonylase
Synthesizes the Active Site CO Ligand of O2-Tolerant [NiFe]
Hydrogenase,
J. Am. Chem. Soc.
2020, 142, 1457-1464 [66]. (Abstract
[67])
[68]
- © 2019 WILEY-VCH
284.
J. Scharfbier, B. M.
Gross, and M. Oestreich,
Stereospecific and Chemoselective
Copper-Catalyzed Deaminative Silylation of Benzylic Ammonium
Triflates,
Angew. Chem. 2020,
132, 1593-1596;
Angew. Chem. Int. Ed.
2020, 59, 1577-1580 [69]. (Abstract [70])
(open access)
[71]
- © 2020 Springer Nature Limited
283.
J. C. L. Walker, H. F.
T. Klare, and M. Oestreich,
Cationic silicon Lewis acids in
catalysis (Perspective),
Nat. Rev. Chem.
2020, 4, 54-62 [72]. (Abstract [73])
Commentary: Nat. Rev. Chem. 2020,
4, 4-5 [74].
[75]
- © 2019 Elsevier
282.
S. C. Richter and M.
Oestreich,
Emerging Strategies for C–H Silylation
(Review),
Trends Chem. 2020,
2, 13-27 [76]. (Abstract [77])
[78]
- © 2019 American Chemical Society
281.
C. Chauvier,
L. Finck, S. Hecht, and M. Oestreich,
General Synthesis and Optical Properties of
N-Aryl-N'-Silyldiazenes,
Organometallics
2019, 38, 4679-4686 [79]. (Abstract
[80])
[81]
- © 2019 Georg Thieme Verlag
280.
J. C. L. Walker and M.
Oestreich,
Ionic Transfer Reactions with
Cyclohexadiene-Based Surrogates (Account),
Synlett 2019, 30, 2216-2232 [82].
(Abstract [83])
[84]
- © 2019 WILEY-VCH
279.
P. Pommerening and M.
Oestreich,
Chiral Modification of the
Tetrakis(pentafluorophenyl)borate Anion with Myrtanyl Groups,
Eur. J. Org. Chem. 2019, 7240-7246 [85].
(Abstract [86])
(open access)
[87]
- © 2019 American Chemical Society
278.
J. Fuchs, E. Irran, P.
Hrobárik, H. F. T. Klare, and M. Oestreich,
Si-H Bond
Activation with Bullock's Cationic Tungsten(II) Catalyst: CO as
Cooperating Ligand,
J. Am. Chem. Soc.
2019, 141, 18845-18850 [88]. (Abstract
[89])
[90]
- © 2019 WILEY-VCH
277.
Q. Wu, A. Roy, E.
Irran, Z.-W. Qu, S. Grimme, H. F. T. Klare, and M. Oestreich,
Catalytic Difunctionalization of Unactivated Alkenes with
Unreactive Hexamethyldisilane through Regeneration of Silylium
Ions,
Angew. Chem. 2019,
131, 17468-17472;
Angew. Chem. Int. Ed.
2019, 58, 17307-17311 [91]. (Abstract
[92])
Highlighted as a "Very Important Paper
(VIP)" by Angewandte Chemie.
(open
access)
Highlighted in SYNFACTS 2019,
15, 1427 [93].
Highlighted in Nachr. Chem.
2021, 69, 38-68 [94].
[95]
- © 2019 Royal Society of Chemistry
276.
T. Kaicharla, B. M.
Zimmermann, M. Oestreich, and J. F. Teichert,
Using alcohols
as simple H2-equivalents for copper-catalysed transfer
hydrogenations,
Chem. Commun.
2019, 55, 13410-13413 [96]. (Abstract
[97])
Published as a preprint: ChemRxiv
2019, DOI: 10.26434/chemrxiv.9731279.v1 [98].
Highlighted in ChemistryViews Magazine [99].
[100]
- © 2019 WILEY-VCH
275.
L. Zhang and M.
Oestreich,
Copper-Catalyzed Enantio- and Diastereoselective
Addition of Silicon Nucleophiles to 3,3-Disubstituted
Cyclopropenes,
Chem. Eur. J. 2019,
25, 14304-14307 [101]. (Abstract [102])
(open
access)
[103]
- © 2019 WILEY-VCH
274.
T. Hiyama and M.
Oestreich (Editors),
Organosilicon Chemistry – Novel
Approaches and Reactions [104], Wiley-VCH, Weinheim,
2019 (568 pages, Hardcover).
ISBN:
978-3-527-34453-6.
Buchbesprechung: Nachr. Chem.
2020, 68, 83.
[105]
- © 2019 WILEY-VCH
273.
P. Shaykhutdinova, S.
Keess, and M. Oestreich,
Cationic Silicon-Based Lewis Acids
in Catalysis [106],
in Organosilicon Chemistry –
Novel Approaches and Reactions [107] (Eds.: T. Hiyama, M.
Oestreich), Wiley-VCH, Weinheim, 2019, 131-170.
(Abstract [108])
[109]
- © 2019 WILEY-VCH
272.
F. Forster and M.
Oestreich,
Metal-Ligand Cooperative Si–H Bond
Activation [110],
in Organosilicon Chemistry – Novel
Approaches and Reactions [111] (Eds.: T. Hiyama, M. Oestreich),
Wiley-VCH, Weinheim, 2019, 115-130. (Abstract
[112])
[113]
- © 2019 WILEY-VCH
271.
J. C. L. Walker and
M. Oestreich,
Lewis Acid-Catalyzed Transfer
Hydromethallylation for the Construction of Quaternary Carbon
Centers,
Angew. Chem. 2019,
131, 15530-15534;
Angew. Chem. Int. Ed.
2019, 58, 15386-15389 [114]. (Abstract
[115])
(open access)
Highlight in SYNFACTS
2019, 15, 1428 [116] as Synfact of
the Month!
[117]
- © 2019 Royal Society of Chemistry
270.
J.-J. Feng, Y. Xu,
and M. Oestreich,
Ligand-Controlled Diastereodivergent,
Enantio- and Regioselective Copper-Catalyzed Hydroxyalkylboration of
1,3-Dienes with Ketones,
Chem. Sci.
2019, 10, 9679-9683 [118]. (Abstract)
Selected for the 2019 Chemical Science HOT Article
Collection
[119]Part of the 2019 ChemSci Pick of the Week
Collection [120]
(open access)
Highlighted in Nat.
Catal. 2019, 2, 833 [121].
Highlighted in
SYNFACTS 2019, 15, 1402
[122].
[123]
- © 2019 AAAS
269.
Q. Wu, E. Irran, R. Müller, M. Kaupp, H.
F. T. Klare, and M. Oestreich,
Characterization of
hydrogen-substituted silylium ions in the condensed phase,
Science 2019, 365, 168-172 [124].
(Abstract [125])
Highlighted in Nachr. Chem.
2019, 67, 47 [126].
Highlighted in
Nachr. Chem. 2020, 68, 50-64
[127].
[128]
- © 2019 WILEY-VCH
268.
W. Mao, W. Xue, E.
Irran, and M. Oestreich,
Copper-Catalyzed Regio- and
Enantioselective Addition of Silicon Grignard Reagents to Alkenes
Activated by Azaaryl Groups,
Angew. Chem.
2019, 131, 10833-10836;
Angew.
Chem. Int. Ed. 2019, 58, 10723-10726
[129]. (Abstract [130])
Selected as a "Hot Paper" by
Angewandte Chemie.
(open access)
Highlighted in
SYNFACTS 2019, 15, 1024
[131].
[132]
- © 2019 WILEY-VCH
267.
J. Seliger and M.
Oestreich,
Making the Silylation of Alcohols Chiral:
Asymmetric Protection of Hydroxy Groups (Minireview),
[OMCOS
20 Special Collection [133]]
Chem. Eur. J.
2019, 25, 9358-9365 [134]. (Abstract
[135])
[136]
- © 2019 WILEY-VCH
266.
S. C. Richter and M.
Oestreich,
Bioinspired Metal-Free Formal Decarbonylation of
α-Branched Aliphatic Aldehydes at Ambient Temperature,
Chem. Eur. J. 2019, 25, 8508-8512
[137]. (Abstract [138])
[139]
- © 2019 American Chemical Society
265.
W. Chen and M.
Oestreich,
Metal-Free Transfer Hydrobromination of C–C
Triple Bonds,
Org. Lett. 2019,
21, 4531-4534 [140]. (Abstract [141])
[142]
- © 2019 WILEY-VCH
264.
J.-J. Feng and M.
Oestreich,
Tertiary α-Silyl Alcohols by Diastereoselective
Coupling of 1,3-Dienes and Acylsilanes Initiated by Enantioselective
Copper-Catalyzed Borylation,
Angew. Chem.
2019, 131, 8295-8299;
Angew. Chem.
Int. Ed. 2019, 58, 8211-8215 [143].
(Abstract [144])
Highlighted in SYNFACTS
2019, 15, 889 [145].
[146]
- © 2019 WILEY-VCH
263.
H. Yi and M.
Oestreich,
Regiodivergent and Stereospecific Aziridine
Opening by Copper-Catalyzed Addition of Silicon Grignard
Reagents,
Chem. Eur. J. 2019,
25, 6505-6507 [147]. (Abstract [148])
Selected as a
"Hot Paper" by Chemistry - A European
Journal.
[149]
- © 2019 WILEY-VCH
262.
W. Xue, W. Mao, L.
Zhang, and M. Oestreich,
Mechanistic Dichotomy of Magnesium-
and Zinc-Based Germanium Nucleophiles in the C(sp3)–Ge
Cross-Coupling with Alkyl Electrophiles,
Angew.
Chem. 2019, 131, 6506-6509;
Angew. Chem. Int. Ed. 2019, 58,
6440-6443 [150]. (Abstract [151])
[152]
- © 2019 Georg Thieme Verlag
261.
P. Shaykhutdinova and M.
Oestreich,
Further Structural Modification of
Sulfur-Stabilized Silicon Cations with Binaphthyl Backbones,
Synthesis 2019, 51, 2221-2229
[153]. (Abstract [154])
[155]
- © 2019 WILEY-VCH
260.
P. Orecchia, W. Yuan,
and M. Oestreich,
Transfer Hydrocyanation of α- and
α,β-Substituted Styrenes Catalyzed by Boron Lewis Acids,
Angew. Chem. 2019, 131,
3617-3621;
Angew. Chem. Int. Ed. 2019,
58, 3579-3583 [156]. (Abstract [157])
[158]
- © 2019 WILEY-VCH
259.
H. Yi, W. Mao, and M.
Oestreich,
Enantioselective Construction of α-Chiral
Silanes by Nickel-Catalyzed C(sp3)–C(sp3)
Cross-Coupling,
Angew. Chem.
2019, 131, 3613-3616;
Angew. Chem.
Int. Ed. 2019, 58, 3575-3578 [159].
(Abstract [160])
Highlighted in SYNFACTS
2019, 15, 506 [161].
[162]
- © 2019 American Chemical Society
258.
L. Süsse, J. H. W.
LaFortune, D. W. Stephan, and M. Oestreich,
Axially Chiral,
Electrophilic Fluorophosphonium Cations: Synthesis, Lewis Acidity, and
Reactivity in the Hydrosilylation of Ketones,
Organometallics 2019, 38, 712-721
[163]. (Abstract [164])
[165]
- © 2019 WILEY-VCH
257.
J. Seliger, X. Dong,
and M. Oestreich,
Kinetic Resolution of Tertiary Propargylic
Alcohols by Enantioselective Cu–H-Catalyzed Si–O Coupling,
Angew. Chem. 2019, 131,
1991-1996;
Angew. Chem. Int. Ed. 2019,
58, 1970-1974 [166]. (Abstract [167])
[168]
- © 2018 American Chemical Society
256.
W. Chen, J. C. L.
Walker, and M. Oestreich,
Metal-Free Transfer
Hydroiodination of C‒C Multiple Bonds,
J. Am. Chem.
Soc. 2019, 141, 1135-1140 [169].
(Abstract [170])
Highlighted in SYNFACTS
2019, 15, 297 [171].
[172]
- © 2018 American Chemical Society
255.
S. Bähr, W. Xue, and
M. Oestreich,
C(sp3)–Si Cross-Coupling
(Perspective),
ACS Catal. 2019,
9, 16-24 [173]. (Abstract [174])
[175]
- © 2018 Georg Thieme Verlag
254.
W. Xue and M. Oestreich,
Silicon Grignard Reagents as Nucleophiles in
Transition-Metal-Catalyzed Allylic Substitution (Feature
Article),
Synthesis 2019, 51,
233-239 [176]. (Abstract [177])
Part of the 50 Years
SYNTHESIS -- Golden Anniversary Issue
(open access)
[178]
- © 2018 American Chemical Society
253.
L. Zhang and M.
Oestreich,
Copper-Catalyzed Cross-Coupling of Vinyliodonium
Salts and Zinc-Based Silicon Nucleophiles,
Org.
Lett. 2018, 20, 8061-8063 [179].
(Abstract [180])
[181]
- © 2018 WILEY-VCH
252.
W. Yuan, P. Orecchia,
and M. Oestreich,
Palladium-Catalyzed Three-Component
Reaction of Dihydrosilanes and Vinyl Iodides in the Presence of
Alcohols: Rapid Assembly of Silyl Ethers of Tertiary Silanes,
Chem. Eur. J. 2018, 24,
19175-19178 [182]. (Abstract [183])
Selected as a "Hot
Paper" by Chemistry - A European Journal.
[184]
- © 2018 American Chemical Society
251.
P. Shaykhutdinova and
M. Oestreich,
Achieving Enantioselectivity in Difficult
Cyclohexa-1,3-diene Diels-Alder Reactions with Sulfur-Stabilized
Silicon Cations as Lewis Acid Catalysts,
Org.
Lett. 2018, 20, 7029-7033 [185].
(Abstract [186])
[187]
- © 2018 American Chemical Society
250.
J. C. L. Walker and M.
Oestreich,
Regioselective Transfer Hydrodeuteration of
Alkenes with an HD Surrogate Using
B(C6F5)3 Catalysis,
Org. Lett. 2018, 20, 6411-6414
[188]. (Abstract [189])
[190]
- © 2018 WILEY-VCH
249.
A. Merk, H.
Großekappenberg, M. Schmidtmann, M.-P. Luecke, C. Lorent, M. Driess,
M. Oestreich, H. F. T. Klare, and T. Müller,
Single-Electron Transfer Reactions in Frustrated
and Conventional Silylium Ion/Phosphane Lewis Pairs,
Angew. Chem. 2018, 130,
15487-15492;
Angew. Chem. Int. Ed.
2018, 57, 15267-15271 [191]. (Abstract
[192])
Highlighted in Nat. Rev. Chem.
2018, 2, 255 [193].
Highlighted in
Nachr. Chem. 2020, 68, 50-64
[194].
[195]
- © 2018 American Chemical Society
248.
M. Vogler,
L. Süsse, J. H. W. LaFortune, D. W. Stephan, and M.
Oestreich,
Electrophilic Phosphonium Cations as Lewis-Acid
Catalysts in Diels–Alder Reactions and Nazarov Cyclizations,
Organometallics 2018, 37,
3303-3313 [196]. (Abstract [197])
[198]
- © 2018 American Chemical Society
247.
H. Hazrati and M.
Oestreich,
Copper-Catalyzed Double C(sp3)–Si
Coupling of Geminal Dibromides: Ionic-to-Radical Switch in the
Reaction Mechanism,
Org. Lett.
2018, 20, 5367-5369 [199]. (Abstract
[200])
[201]
- © 2018 WILEY-VCH
246.
W. Xue, R. Shishido,
and M. Oestreich,
Bench-Stable Stock Solutions of Silicon
Grignard Reagents: Application to Iron- and Cobalt-Catalyzed Radical
C(sp3)–Si Cross-Coupling Reactions,
Angew.
Chem. 2018, 130, 12318-12322;
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Highlighted as a
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245.
F. Forster and M.
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Bioinspired Catalytic Generation of Main-Group
Electrophiles by Cooperative Bond Activation (Account),
CHIMIA 2018, 72, 584-588
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244.
F. Forster, V. M.
Rendón López, and M. Oestreich,
Z-Selective
Hydrostannylation of Terminal and Internal C–C Triple Bonds
Initiated by the Trityl Cation,
Organometallics
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243.
L. Süsse, M. Vogler,
M. Mewald, B. Kemper, E. Irran, and M. Oestreich,
Enantioselective Nazarov Cyclizations Catalyzed by an Axial
Chiral, C6F5-Substituted Boron Lewis Acid,
Angew. Chem. 2018, 130,
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Angew. Chem. Int. Ed.
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242.
X. Dong, Y. Kita, and
M. Oestreich,
Kinetic Resolution of α-Hydroxy-Substituted
Oxime Ethers by Enantioselective Cu–H-Catalyzed Si–O
Coupling,
Angew. Chem. 2018,
130, 10888-10891;
Angew. Chem. Int. Ed.
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Selected as a "Hot Paper" by Angewandte
Chemie.
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241.
J.-J. Feng and M.
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Copper-Catalyzed Silylation of
C(sp3)-H Bonds Adjacent to Amide Nitrogen Atoms,
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240.
Q. Wu, Z.-W. Qu, L.
Omann, E. Irran, H. F. T. Klare, and M. Oestreich,
Cleavage
of Unactivated Si‒C(sp3) Bonds with Reed's Carborane
Acids: Formation of Known and Unknown Silylium Ions,
Angew. Chem. 2018, 130,
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Angew. Chem. Int. Ed. 2018,
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239.
L. Omann, B.
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Thermodynamic versus kinetic control in substituent
redistribution reactions of silylium ions steered by the
counteranion,
Chem. Sci. 2018,
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238.
L. Omann, Z.-W. Qu,
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Electrophilic Formylation of Arenes by Silylium Ion Mediated
Activation of Carbon Monoxide,
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237.
P. Shaykhutdinova, S.
Kemper, and M. Oestreich,
Refinement of the Catalyst
Backbone of Chiral Intramolecular Silicon-Sulfur Lewis Pairs: Improved
Enantioselectivity in the Diels-Alder Reaction of Cyclohexa-1,3-diene
and Chalcone Derivatives,
Eur. J. Org. Chem.
2018, 2896-2901 [231]. (Abstract [232])
Part of
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236.
W. Yuan, P. Smirnov,
and M. Oestreich,
Custom Hydrosilane Synthesis Based on
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4, 1443-1450 [236]. (Abstract [237])
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235.
P. Pommerening, T.
Stahl, and M. Oestreich,
Direct Acetophenone-Acetophenone
Crossed Aldol Reaction and Aldol Self Reaction Promoted by a Tethered
Ru-S Complex,
Eur. J. Org. Chem.
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234.
S. Bähr and M.
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A Neutral Ru(II) Hydride Complex for the Regio-
and Chemoselective Reduction of N-Silylpyridinium Ions,
Chem. Eur. J. 2018, 24, 5613-5622
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233.
S. Bähr and M.
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The Electrophilic Aromatic Substitution Approach
to C-H Silylation and C-H Borylation
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232.
F. Forster, V. M.
Rendón López, and M. Oestreich,
Catalytic Dehydrogenative
Stannylation of C(sp)-H Bonds Involving Cooperative Sn-H Bond
Activation of Hydrostannanes,
J. Am. Chem. Soc.
2018, 140, 1259-1262 [249]. (Abstract
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231.
J. Scharfbier, H.
Hazrati, E. Irran, and M. Oestreich,
Copper-Catalyzed
Substitution of α-Triflyloxy Nitriles and Esters with
Silicon Nucleophiles under Inversion of the Configuration,
Org. Lett. 2017, 19, 6562-6565
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230.
J. Fuchs, H. F. T.
Klare, and M. Oestreich,
Two-Silicon Cycle for Carbonyl
Hydrosilylation with Nikonov’s Cationic Ruthenium(II) Catalyst,
ACS Catal. 2017, 7, 8338-8342
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229.
F. Forster, T. T.
Metsänen, E. Irran, P. Hrobárik, and M. Oestreich,
Cooperative Al-H Bond Activation in DIBAL-H: Catalytic
Generation of an Alumenium-Ion-Like Lewis Acid for Hydrodefluorinative
Friedel-Crafts Alkylation,
J. Am. Chem. Soc.
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228.
M.-P. Luecke, D.
Porwal, A. Kostenko, Y.-P. Zhou, S. Yao, M. Keck, C. Limberg, M.
Oestreich, and M. Driess,
Bis(silylenyl)-substituted
ferrocene-stabilized η6-arene iron(0) complexes:
synthesis, structure and catalytic application,
Dalton
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(Abstract)
Featured on the Front Cover of Dalton
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227.
S. Bähr, H. Ogasawara,
S. Yamaguchi, and M. Oestreich,
An Expedient Procedure for
the Synthesis of Benzo[4,5]silolo[2,3-b]thiophenes and
Related Systems,
Organometallics
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226.
S. Wübbolt and M.
Oestreich,
Exhaustive Chemoselective Reduction of Nitriles
by Catalytic Hydrosilylation Involving Cooperative Si-H Bond
Activation
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Catalysis [269]),
Synlett 2017,
28, 2411-2414 [270]. (Abstract [271])
Preface by
M. Oestreich,
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225.
W. Yuan, P. Orecchia,
and M. Oestreich,
Cyclohexa-1,3-diene-based dihydrogen and
hydrosilane surrogates in
B(C6F5)3-catalysed transfer
processes,
Chem. Commun. 2017,
53, 10390-10393 [275]. (Abstract)
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224.
W. Xue and M.
Oestreich,
Copper-Catalyzed Decarboxylative Radical
Silylation of Redox-Active Aliphatic Carboxylic Acid Derivatives,
Angew. Chem. 2017, 129,
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Angew. Chem. Int. Ed.
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223.
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B(C6F5)3-Catalyzed Reduction of
Sulfoxides and Sulfones to Sulfides with Hydrosilanes,
Synthesis 2017, 49, 4698-4702
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222.
S. Keess and M. Oestreich,
Tri(cyclohexa-2,5-dien-1-yl)silane,
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221.
Q. Yin, Y. Soltani, R.
L. Melen, and M. Oestreich,
BArF3-Catalyzed Imine Hydroboration with
Pinacolborane Not Requiring the Assistance of an Additional Lewis
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Organometallics 2017,
36, 2381-2384 [286]. (Abstract [287])
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220.
S. Keess and M.
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Cyclohexa-1,4-dienes in transition-metal-free
ionic transfer processes (Minireview),
Chem.
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219.
Q. Yin and M.
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Photocatalysis Enabling Acceptorless
Dehydrogenation of Benzofused Saturated Rings at Room Temperature
(Highlight),
Angew. Chem. 2017,
129, 7824-7826;
Angew. Chem. Int. Ed.
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218.
X. Dong, A.
Weickgenannt, and M. Oestreich,
Broad-spectrum kinetic
resolution of alcohols enabled by Cu–H-catalysed dehydrogenative
coupling with hydrosilanes,
Nat. Commun.
2017, 8, 15547 [294]. (Abstract)
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217.
W.-B. Liu, D. P.
Schuman, Y.-F. Yang, A. A. Toutov, Y. Liang, H. F. T. Klare, N.
Nesnas, M. Oestreich, D. G. Blackmond, S. C. Virgil, S. Banerjee, R.
N. Zare, R. H. Grubbs, K. N. Houk, and B. M. Stoltz,
Potassium tert-Butoxide-Catalyzed Dehydrogenative C–H
Silylation of Heteroaromatics: A Combined Experimental and
Computational Mechanistic Study,
J. Am. Chem. Soc.
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216.
L. Omann, C. D. F.
Königs, H. F. T. Klare, and M. Oestreich,
Cooperative
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Acc. Chem. Res. 2017, 50,
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215.
L.-Y. Jiao and M.
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C-H Bond Functionalization at the Benzene Core of
Indoles and Indolines (Excluding C-2 and C-3) [302],
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214.
P. Pommerening, J.
Mohr, J. Friebel, and M. Oestreich,
Synthesis of a Chiral
Borate Counteranion, its Trityl Salt, and Application Thereof in
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Eur. J. Org. Chem.
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213.
S. Wübbolt, M. S.
Maji, E. Irran, and M. Oestreich,
A Tethered Ru–S Complex
with an Axial Chiral Thiolate Ligand for Cooperative Si‒H Bond
Activation: Application to Enantioselective Imine Reduction,
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Chem. Eur. J. 2017, 23,
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212.
S. Keess and M.
Oestreich,
3-tert-Butyl-Substituted Cyclohexa-1,4-dienes as
Isobutane Equivalents in the B(C6F5)3-Catalyzed Transfer
Hydro-tert-Butylation of Alkenes,
[Collaborative Research
Center (SFB 858) on Cooperative Effects [312]]
Chem. Eur.
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211.
L. B. Delvos and M.
Oestreich,
Silylboron Reagents (Volume 4, Product Class
7, Section 4.4.7),
in Science of Synthesis Knowledge Updates
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210.
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Access to Fully Alkylated Germanes by
B(C6F5)3-Catalyzed Transfer
Hydrogermylation of Alkenes,
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209.
Q. Yin, H. F. T.
Klare, and M. Oestreich,
Catalytic Friedel–Crafts C–H
Borylation of Electron-Rich Arenes: Dramatic Rate Acceleration by
Added Alkenes,
Angew. Chem. 2017,
129, 3766-3771;
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208.
I. Chatterjee, D.
Porwal, and M. Oestreich,
B(C6F5)3-Catalyzed Chemoselective
Defunctionalization of Ether-Containing Primary Alkyl Tosylates with
Hydrosilanes,
Angew. Chem. 2017,
129, 3438-3441;
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207.
S. Bähr and M.
Oestreich,
Hidden Enantioselective Hydrogenation of N-Silyl
Enamines and Silyl Enol Ethers in Net C=N and C=O Hydrosilylations
Catalyzed by Ru–S Complexes with One Monodentate Chiral Phosphine
Ligand,
Organometallics 2017,
36, 935-943 [329]. (Abstract [330])
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206.
L. Omann and M.
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Catalytic Access to Indole-Fused Benzosiloles by
2-Fold Electrophilic C–H Silylation with Dihydrosilanes,
Organometallics 2017, 36, 767-776
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Featured on the Cover of
Organometallics [334].
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205.
C. Fopp, K. Isaac, E.
Romain, F. Chemla, F. Ferreira, O. Jackowski, M. Oestreich, and A.
Perez-Luna,
Stereodivergent Synthesis of
beta-Heteroatom-Substituted Vinylsilanes by Sequential
Silylzincation-Cu(I)-Mediated Electrophilic Substitution (Feature
Article),
Synthesis 2017, 49,
724-735 [336]. (Abstract [337])
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204.
S. Bähr and M.
Oestreich,
Electrophilic Aromatic Substitution with Silicon
Electrophiles: Catalytic Friedel-Crafts C-H Silylation
(Minireview),
Angew. Chem. 2017,
129, 52-59;
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2017, 56, 52-59 [339]. (Abstract
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203.
H. F. T. Klare and M. Oestreich,
Teaching nature the unnatural (Perspective),
Science 2016, 354, 970 [342].
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202.
W. Xue, Z.-W. Qu. S.
Grimme, and M. Oestreich,
Copper-Catalyzed Cross-Coupling of
Silicon Pronucleophiles with Unactivated Alkyl Electrophiles Coupled
with Radical Cyclization,
J. Am. Chem. Soc.
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201.
J. Mohr and M.
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Balancing C=C Functionalization and C=O Reduction
in Cu-H Catalysis (Highlight),
Angew. Chem.
2016, 128, 12330-12332;
Angew.
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200.
P. Shaykhutdinova and
M. Oestreich,
Enantioselective Diels−Alder Reactions of
Cyclohexa-1,3-diene and Chalcones Catalyzed by Intramolecular
Silicon–Sulfur Lewis Pairs as Chiral Lewis Acids,
Organometallics 2016, 35,
2768-2771 [351]. (Abstract [352])
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199.
Q. Yin, S. Kemper, H.
F. T. Klare, and M. Oestreich,
Boron Lewis Acid-Catalyzed
Hydroboration of Alkenes with Pinacolborane: BArF3 Does What B(C6F5)3
Cannot Do!,
Chem. Eur. J. 2016,
22, 13840-13844 [354]. (Abstract [355])
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198.
P. Smirnov and M.
Oestreich,
Merging Platinum-Catalyzed Alkene Hydrosilylation
with SiH4 Surrogates: Salt-Free Preparation of
Trihydrosilanes,
Organometallics
2016, 35, 2433-2434 [357]. (Abstract
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197.
Q.-A. Chen, H. F. T.
Klare, and M. Oestreich,
Brønsted Acid-Promoted Formation
of Stabilized Silylium Ions for Catalytic Friedel–Crafts C–H
Silylation,
J. Am. Chem. Soc.
2016, 138, 7868-7871 [360]. (Abstract
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ACS AuthorChoice (open access)
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196.
D. Porwal and M.
Oestreich,
B(C6F5)3-Catalyzed Reduction of Aromatic and
Aliphatic Nitro Groups with Hydrosilanes,
Eur. J. Org.
Chem. 2016, 3307-3309 [363]. (Abstract
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195.
I. Chatterjee and M.
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Brønsted Acid-Catalyzed Transfer Hydrogenation
of Imines and Alkenes Using Cyclohexa-1,4-dienes as Dihydrogen
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18, 2463-2466 [366]. (Abstract [367])
ACS AuthorChoice
(open access)
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2016, 12, 971 [368].
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194.
L. Süsse, J. Hermeke,
and M. Oestreich,
The Asymmetric Piers Hydrosilylation,
J. Am. Chem. Soc. 2016, 138,
6940-6943 [370]. (Abstract [371])
ACS AuthorChoice (open
access)
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12, 833 [372].
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193.
A. Lefranc, Z.-W. Qu,
S. Grimme, and M. Oestreich,
Hydrogenation and Transfer
Hydrogenation Promoted by Tethered Ru‒S Complexes: From Cooperative
Dihydrogen Activation to Hydride Abstraction/Proton Release from
Dihydrogen Surrogates,
Chem. Eur. J.
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192.
C. Fopp, E. Romain, K.
Isaac, F. Chemla, F. Ferreira, O. Jackowski, M. Oestreich, and A.
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Stereodivergent Silylzincation of
α-Heteroatom-Substituted Alkynes,
Org.
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191.
M. Mehta, I. Garcia de
la Arada, M. Perez, D. Porwal, M. Oestreich, and D. W. Stephan,
Metal-Free Phosphine Oxide Reductions Catalyzed by B(C6F5)3 and
Electrophilic Fluorophosphonium Cations,
Organometallics 2016, 35,
1030-1035 [381]. (Abstract [382])
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190.
S. Bähr, A. Simonneau,
E. Irran, and M. Oestreich,
An Air-Stable Dimeric Ru-S
Complex with an NHC as Ancillary Ligand for Cooperative Si-H Bond
Activation,
Organometallics 2016,
35, 925-928 [384]. (Abstract [385])
ACS AuthorChoice
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189.
J. Scharfbier and M.
Oestreich,
Copper-Catalyzed Si-B Bond Activation in the
Nucleophilic Substitution of Primary Aliphatic Triflates,
Synlett 2016, 27, 1274-1276
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188.
A. Hensel and M. Oestreich,
Asymmetric Addition of Boron and Silicon Nucleophiles
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in Electronic Encyclopedia of Reagents for Organic Synthesis
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186.
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T. Klare, R. Fröhlich, and M. Oestreich,
Planar Chiral,
Ferrocene-Stabilized Silicon Cations,
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185.
Q. Yin, H. F. T.
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Friedel–Crafts-Type Intermolecular
C–H Silylation of Electron-Rich Arenes Initiated
by Base-Metal Salts,
Angew. Chem.
2016, 128, 3256-3260;
Angew. Chem.
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184.
L.-Y. Jiao, A. V.
Ferreira, and M. Oestreich,
Phosphinic Amide as Directing
Group Enabling Palladium(II)-Catalyzed ortho C-H Alkenylation of
Anilines without and with Alkylation at the Nitrogen Atom
(Special Issue on Catalysis and Transformation of Complex
Molecules),
Chem. Asian J. 2016,
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183.
M. Oestreich,
Transfer Hydrosilylation (Minireview),
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Catalytic Electrophilic C-H Silylation of
Pyridines Enabled by Temporary Dearomatization,
Angew.
Chem. 2015, 127, 16103-16106;
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181.
J. Mohr, D. Porwal,
I. Chatterjee, and M. Oestreich,
Extending the Scope of the
B(C6F5)3-Catalyzed C=N Bond Reduction: Hydrogenation of Oxime Ethers
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180.
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Peripheral mechanism of a carbonyl hydrosilylation catalyzed
by an SiNSi iron pincer complex,
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179.
T. Fallon and M.
Oestreich,
A Constellation of Deuterium-Labeled Silanes
as a Simple Mechanistic Probe not Requiring Absolute Configuration
Determination
(Special Issue: Chemistry in Germany
and Israel),
Angew. Chem. 2015,
127, 12666-12670;
Angew. Chem. Int. Ed.
2015, 54, 12488-12491 [415]. (Abstract
[416])
Highlighted as a "Very Important Paper
(VIP)" by Angewandte Chemie.
Featured on
the Back Cover of Angewandte Chemie [417].
[418]
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178.
I. Chatterjee, Z.-W.
Qu, S. Grimme, and M. Oestreich,
B(C6F5)3-Catalyzed
Transfer of Dihydrogen from One Unsaturated Hydrocarbon to
Another,
Angew. Chem. 2015,
127, 12326-12330;
Angew. Chem. Int. Ed.
2015, 54, 12158-12162 [419]. (Abstract
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177.
A. Simonneau, T.
Biberger, and M. Oestreich,
The
Cyclohexadienyl-Leaving-Group Approach toward Donor-Stabilized
Silylium Ions,
Organometallics
2015, 34, 3927-3929 [422]. (Abstract
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ACS AuthorChoice (open access)
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176.
A. Simonneau
and M. Oestreich,
Formal SiH4 chemistry using stable and
easy-to-handle surrogates,
Nat. Chem. 2015, 7, 816-822
[425]. (Abstract [426])
Highlighted in SYNFACTS
2015, 11, 1158 [427].
Highlighted in
Nachr. Chem. 2016, 64, 6.
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175.
L. Omann and M.
Oestreich,
A Catalytic SEAr Approach to Dibenzosiloles
Functionalized at Both Benzene Cores,
Angew.
Chem. 2015, 127, 10414-10418;
Angew. Chem. Int. Ed. 2015, 54,
10276-10279 [429]. (Abstract [430])
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- © 2015 American Chemical Society
174.
V. H. G. Rohde, M. F.
Müller, and M. Oestreich,
Intramolecularly
Sulfur-Stabilized Silicon Cations with Chiral Binaphthyl Backbones:
Synthesis of Three Different Motifs and Their Application in
Enantioselective Diels-Alder Reactions,
Organometallics 2015, 34,
3358-3373 [432]. (Abstract [433])
ACS AuthorChoice (open
access)
[434]
- © 2015 Royal Society of Chemistry
173.
T. Stahl, P.
Hrobárik, C. D. F. Königs, Y. Ohki, K. Tatsumi, S. Kemper, M. Kaupp,
H. F. T. Klare, and M. Oestreich,
Mechanism of the
cooperative Si–H bond activation at
Ru–S bonds,
Chem.
Sci. 2015, 6, 4324-4334 [435].
(Abstract)
(open access)
[436]
- © 2015 WILEY-VCH
172.
A. Hensel and M.
Oestreich,
Asymmetric Catalysis with Silicon-Based
Cuprates: Enantio- and Regioselective Allylic Substitution of Linear
Precursors,
Chem. Eur. J.
2015, 21, 9062-9065 [437]. (Abstract
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Highlighted in SYNFACTS 2015,
11, 829 [439].
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171.
M. Pareek, T. Fallon,
and M. Oestreich,
Platinum(0)-Catalyzed Indolyne
Insertion into Bis(pinacolato)diboron Followed by Site-Selective
Suzuki-Miyaura Cross-Coupling,
Org. Lett.
2015, 17, 2082-2085 [441]. (Abstract
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ACS AuthorChoice (open access)
Highlighted to
SYNFACTS 2015, 11, 855
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170.
A. Simonneau and M.
Oestreich,
Fascinating Hydrogen Atom Transfer Chemistry
of Alkenes Inspired by Problems in Total Synthesis
(Highlight),
Angew. Chem. 2015,
127, 3626-3628;
Angew. Chem. Int. Ed.
2015, 54, 3556-3558 [445]. (Abstract
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- © 2015 Georg Thieme Verlag
169.
L. B. Delvos and M.
Oestreich,
Temperature-Dependent Direct
Enantioconvergent Silylation of a Racemic Cyclic Allylic Phosphate by
Copper(I)-Catalyzed Allylic Substitution (Feature Article),
Synthesis 2015, 47, 924-933
[448]. (Abstract [449])
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- © 2015 WILEY-VCH
168.
X. Zhou, K. Szeker,
L.-Y. Jiao, M. Oestreich, I. A. Mikhailopulo, and P. Neubauer,
Synthesis of 2,6-Dihalogenated Purine Nucleosides by
Thermostable Nucleoside Phosphorylases,
Adv.
Synth. Catal. 2015, 357, 1237-1244
[451]. (Abstract [452])
167.
M. Oestreich and A.
Simonneau,
Use of cyclohexa-2,5-dien-1-yl-silanes as
precursors for gaseous hydrosilanes,
Eur. Pat.
Appl. 2015, EP 2845857 (PCT Int. Appl.
WO 2015/036309 A1).
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166.
S. Keess, A. Simonneau,
and M. Oestreich,
Direct and Transfer Hydrosilylation
Reactions Catalyzed by Fully or Partially Fluorinated Triarylboranes:
A Systematic Study,
Organometallics
2015, 34, 790-799 [454]. (Abstract [455])
ACS AuthorChoice (open access)
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- © 2015 Royal Society of Chemistry
165.
M. Oestreich, J.
Hermeke, and J. Mohr,
A unified survey of Si-H and H-H
bond activation catalysed by electron-deficient boranes
(Review),
Chem. Soc. Rev. 2015,
44, 2202-2220 [457]. (Abstract)
(open access)
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- © 2014 American Chemical Society
164.
T. T. Metsänen and M.
Oestreich,
Temperature-Dependent Chemoselective
Hydrosilylation of Carbon Dioxide to Formaldehyde or Methanol
Oxidation State,
Organometallics
2015, 34, 543-546 [459]. (Abstract [460])
Featured on the Cover of Organometallics [461].
[462]
- © 2014 WILEY-VCH
163.
I. Chatterjee and M.
Oestreich,
B(C6F5)3-Catalyzed Transfer Hydrogenation of
Imines and Related Heteroarenes Using Cyclohexa-1,4-dienes as a
Dihydrogen Source,
Angew. Chem.
2015, 127, 1988-1991;
Angew. Chem.
Int. Ed. 2015, 54, 1965-1968 [463].
(Abstract [464])
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162.
L.-Y. Jiao, P. Smirnov,
and M. Oestreich,
Exceptionally Mild
Palladium(II)-Catalyzed Dehydrogenative C-H/C-H Arylation of Indolines
at the C-7 Position under Air,
Org. Lett.
2014, 16, 6020-6023 [466]. (Abstract
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- © 2014 American Chemical Society
161.
J. Hermeke, M. Mewald,
E. Irran, and M. Oestreich,
Chemoselective Tin-Boron
Exchange Aided by the Use of Dummy Ligands at the Tin Atom,
Organometallics 2014, 33,
5097-5100 [469]. (Abstract [470])
[471]
- © 2014 WILEY-VCH
160.
J. Mohr and M.
Oestreich,
B(C6F5)3-Catalyzed Hydrogenation of Oxime
Ethers without Cleavage of the N-O Bond,
Angew.
Chem. 2014, 126, 13494-13497;
Angew. Chem. Int. Ed. 2014, 53,
13278-13281 [472]. (Abstract [473])
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- © 2014 WILEY-VCH
159.
E. Romain, C. Fopp,
F. Chemla, F. Ferreira, O. Jackowski, M. Oestreich, and A. Perez-Luna,
Trans-Selective Radical Silylzincation of
Ynamides,
Angew. Chem. 2014,
126, 11515-11519;
Angew. Chem. Int. Ed.
2014, 53, 11333-11337 [475]. (Abstract
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2015, 11, 79 [477].
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158.
L. B. Delvos, A. Hensel,
and M. Oestreich,
McQuade's 6-Membered NHC-Copper(I)
Complexes for Catalytic Asymmetric Silyl Transfer,
Synthesis 2014, 46, 2957-2964
[479]. (Abstract [480])
[481]
- © WILEY-VCH
157.
C. K. Hazra, C. Fopp, and M. Oestreich,
Copper(I)-Catalyzed Regioselective Addition of Nucleophilic
Silicon Across Terminal and Internal Carbon-Carbon Triple
Bonds,
Chem. Asian J. 2014,
9, 3005-3010 [482]. (Abstract [483])
[484]
- © 2014 American Chemical Society
156.
V. H. G. Rohde, P.
Pommerening, H. F. T. Klare, and M. Oestreich,
Intramolecularly Sulfur-Stabilized Silicon Cations as Lewis
Acid Catalysts,
Organometallics
2014, 33, 3618-3628 [485]. (Abstract
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155.
K. M. Redies, T.
Fallon, and M. Oestreich,
En Route to Stable
All-Carbon-Substituted Silylenes: Synthesis and Reactivity of a
Bis(α-spirocyclopropyl)silylene,
Organometallics 2014, 33,
3235-3238 [488]. (Abstract [489])
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154.
T. T. Metsänen, P.
Hrobárik, H. F. T. Klare, M. Kaupp, and M. Oestreich,
Insight into the Mechanism of Carbonyl Hydrosilylation
Catalyzed by Brookhart's Cationic Iridium(III) Pincer
Complex,
J. Am. Chem. Soc.
2014, 136, 6912-6915 [491]. (Abstract
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Highlighted in ChemCatChem 2014,
6, 2486-2489 [493].
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153.
J. Hermeke, H. F. T.
Klare, and M. Oestreich,
Direct Catalytic Access to
N-Silylated Enamines from Enolizable Imines and Hydrosilanes
by Base-Free Dehydrogenative Si–N Coupling
(ISOS XVII
Conference Issue New Frontiers and Challenges in Silicon
Chemistry [495]),
Chem. Eur. J.
2014, 20, 9250-9254 [496]. (Abstract
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Editorial by M. Driess and M. Oestreich,
Chem. Eur. J. 2014, 20, 9144-9145
[498]. (Abstract [499])
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152.
A. Hensel, K. Nagura,
L. B. Delvos, and M. Oestreich,
Enantioselective Addition
of Silicon Nucleophiles to Aldimines Using a Preformed NHC-Copper(I)
Complex as the Catalyst,
Angew. Chem.
2014, 126, 5064-5067;
Angew. Chem.
Int. Ed. 2014, 53, 4964-4967 [501].
(Abstract [502])
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2014, 10, 840 [503].
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151.
J. Mohr, M. Durmaz, E.
Irran, and M. Oestreich,
Tris(5,6,7,8-tetrafluoronaphthalen-2-yl)borane, a Partially
Fluorinated Boron Lewis Acid with Fluorination Distal to the Boron
Atom,
Organometallics 2014,
33, 1108-1111 [505]. (Abstract [506])
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150.
S. R. Kandukuri,
L.-Y. Jiao, A. B. Machotta, and M. Oestreich,
Diastereotopic
Group Selection in Hydroxy-Directed Intramolecular C-H Alkenylation of
Indole under Oxidative Palladium(II) Catalysis
(Special
Thematic Issue on Directed C-H Functionalization),
Adv. Synth. Catal. 2014, 356,
1597-1609 [508]. (Abstract [509])
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149.
U. Hennecke, C. Rösner,
T. Wald, T. Robert, and M. Oestreich,
Addition Reactions
with Formation of Carbon-Halogen Bonds [511],
in
Comprehensive Organic Synthesis II (Eds.: G. Molander and P.
Knochel), Elsevier, Oxford, 2014, Vol. 7,
638-691 (Abstract [512]).
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148.
A. Simonneau, J.
Friebel, and M. Oestreich,
Salt-Free Preparation of
Trimethylsilyl Ethers by B(C6F5)3-Catalyzed Transfer Silylation by
Using a Me3SiH Surrogate,
Eur. J. Org. Chem.
2014, 2077-2083 [514]. (Abstract [515])
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147.
M. Oestreich,
Breaking News on the Enantioselective Intermolecular Heck
Reaction (Highlight),
Angew. Chem.
2014, 126, 2314-2317;
Angew. Chem.
Int. Ed. 2014, 53, 2282-2285 [517].
(Abstract [518])
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146.
A. de Meijere, S. Bräse,
and M. Oestreich (Editors),
Metal-Catalyzed Cross-Coupling
Reactions and More [520], Wiley-VCH, Weinheim,
2014 (1576 pages, Hardcover).
ISBN:
978-3-527-33154-3.
Book Review: Angew. Chem.
2014, 126, 13215-13216 [521]; Angew.
Chem. Int. Ed. 2014, 53, 13001-13002
[522].
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145.
A. R. Nödling, K.
Müther, V. H. G. Rohde, G. Hilt, and M. Oestreich,
Ferrocene-Stabilized Silicon Cations as Catalysts for
Diels-Alder Reactions: Attempted Experimental Quantification of Lewis
Acidity and ReactIR Kinetic Analysis,
Organometallics 2014, 33, 302-308
[524]. (Abstract [525])
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144.
L.-Y. Jiao and M.
Oestreich,
Oxidative Palladium(II)-Catalyzed C-7 Alkenylation
of Indolines,
Org. Lett. 2013,
15, 5374-5377 [527]. (Abstract [528])
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143.
J. Hermeke, M. Mewald,
and M. Oestreich,
Experimental Analysis of the Catalytic
Cycle of the Borane-Promoted Imine Reduction with Hydrosilanes:
Spectroscopic Detection of Unexpected Intermediates and a Refined
Mechanism,
J. Am. Chem. Soc.
2013, 135, 17537-17546 [530]. (Abstract
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- © 2013 Teknoscienze S.r.l.
142.
L. B. Delvos and M.
Oestreich,
Direct and Indirect Synthesis of alpha-Chiral
Allylic Silanes by Asymmetric Allylic Substitution with Silicon and
Carbon Nucleophiles,
Chemistry TODAY / Chimica
OGGI 2013, 31, 74-77 [533]
(September/October issue).
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141.
K. Müther, P.
Hrobárik, V. Hrobáriková, M. Kaupp, and M. Oestreich,
The Family of Ferrocene-Stabilized Silylium Ions: Synthesis,
29Si NMR Characterization, Lewis Acidity, Substituent Scrambling, and
Quantum-Chemical Analyses,
Chem. Eur. J.
2013, 19, 16579-16594 [535]. (Abstract
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Highlighted as a "Very Important Paper
(VIP)" by Chemistry - A European
Journal.
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140.
A. Simonneau and M.
Oestreich,
3-Silylated Cyclohexa-1,4-dienes as Precursors for
Gaseous Hydrosilanes: The B(C6F5)3-Catalyzed Transfer Hydrosilylation
of Alkenes,
Angew. Chem. 2013,
125, 12121-12124;
Angew. Chem. Int. Ed.
2013, 52, 11905-11907 [538]. (Abstract
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2014, 10, 73 [540].
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139.
T. Stahl, K. Müther,
Y. Ohki, K. Tatsumi, and M. Oestreich,
Catalytic
Generation of Borenium Ions by Cooperative B-H Bond Activation: The
Elusive Direct Electrophilic Borylation of Nitrogen Heterocycles with
Pinacolborane,
J. Am. Chem. Soc.
2013, 135, 10978-10981 [542]. (Abstract
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9, 1216 [544].
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138.
C. D. F. Königs, H.
F. T. Klare, and M. Oestreich,
Catalytic 1,4-Selective
Hydrosilylation of Pyridines and Benzannulated Congeners,
Angew. Chem. 2013, 125,
10260-10263;
Angew. Chem. Int. Ed.
2013, 52, 10076-10079 [546]. (Abstract
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Selected as a "Hot Paper" by Angewandte
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137.
L.-Y. Jiao and M.
Oestreich,
Oxidative Palladium(II)-Catalyzed
Dehydrogenative C–H/C–H Cross-Coupling of 2,3-Substituted
Indolines with Arenes at the C-7 Position,
Chem.
Eur. J. 2013, 19, 10845-10848 [549].
(Abstract [550])
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136.
C. K. Hazra, E.
Irran, and M. Oestreich,
Regio- and Diastereoselective,
Copper(I)-Catalyzed Allylic Substitution of δ-Hydroxy Allylic
Chlorides by Silicon Nucleophile,
Eur. J. Org.
Chem. 2013, 4903-4908 [552]. (Abstract
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135.
T. Stahl, H. F. T.
Klare, and M. Oestreich,
Main-Group Lewis Acids for C–F
Bond Activation (Perspective),
ACS Catal.
2013, 3, 1578-1587 [555]. (Abstract
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Featured on the Cover of ACS Catalysis
[557].
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134.
K. Müther, J. Mohr,
and M. Oestreich,
Silylium Ion Promoted Reduction of Imines
with Hydrosilanes
(Special Issue on Applications of
Electrophilic Main Group Organometallic Molecules),
Organometallics 2013, 32,
6643-6646 [559]. (Abstract [560])
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133.
T. Robert and M.
Oestreich,
Si-H Bond Activation: Bridging Lewis Acid
Catalysis with Brookhart's Iridium(III) Pincer Complex and
B(C6F5)3 (Highlight),
Angew. Chem.
2013, 125, 5324-5326;
Angew. Chem.
Int. Ed. 2013, 52, 5216-5218 [562].
(Abstract [563])
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132.
L. B. Delvos, D. J.
Vyas, and M. Oestreich,
Asymmetric Synthesis of α-Chiral
Allylic Silanes by Enantioconvergent γ-Selective Copper(I)-Catalyzed
Allylic Silylation,
Angew. Chem.
2013, 125, 4748-4751;
Angew. Chem.
Int. Ed. 2013, 52, 4650-4653 [565].
(Abstract [566])
Highlighted in SYNFACTS
2013, 9, 744 [567].
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131.
C. D. F. Königs,
M. F. Müller, N. Aiguabella, H. F. T. Klare, and M. Oestreich,
Catalytic dehydrogenative Si–N coupling of
pyrroles, indoles, carbazoles as well as anilines with hydrosilanes
without added base,
Chem. Commun.
2013, 49, 1506-1508 [569]. (Abstract
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130.
T. Stahl, H. F. T.
Klare, and M. Oestreich,
C(sp3)–F Bond
Activation of CF3-Substituted Anilines with Catalytically Generated
Silicon Cations: Spectroscopic Evidence for a Hydride-Bridged
Ru–S Dimer in the Catalytic Cycle,
J. Am. Chem. Soc. 2013, 135,
1248-1251 [572]. (Abstract [573])
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129.
M. Oestreich, E.
Hartmann, and M. Mewald,
Activation of the Si-B Interelement
Bond: Mechanism, Catalysis, and Synthesis (Review),
Chem. Rev. 2013, 113,
402-441 [575]. (Abstract [576])
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128.
W. Nie, H.
F. T. Klare, M. Oestreich, R. Fröhlich, G. Kehr, and G. Erker,
Reversible Heterolytic Si–H Bond Activation by
an Intramolecular Frustrated Lewis Pair
(Special Issue
dedicated to Professor Heribert Offermanns),
Z.
Naturforsch. 2012, 67b, 987-994 [578].
(Abstract [579])
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127.
M. Mewald and M.
Oestreich,
Illuminating the Mechanism of the
Borane-Catalyzed Hydrosilylation of Imines with Both an Axially Chiral
Borane and Silane,
Chem. Eur. J.
2012, 18, 14079-14084 [581]. (Abstract
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126.
S. R. Kandukuri and M.
Oestreich,
Aerobic Palladium(II)-Catalyzed Dehydrogenation
of Cyclohexene-1-carbonyl Indole Amides: An Indole-Directed
Aromatization,
J. Org. Chem.
2012, 77, 8750-8755 [584]. (Abstract
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125.
T. H. Wöste and M.
Oestreich,
Hemilabile BINAP(O) as a Chiral Ligand in
Desymmetrizing Mizoroki-Heck Cyclizations,
ChemCatChem 2012, 4,
2096-2101 [587]. (Abstract [588])
Highlighted in ChemViews
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124.
C. K. Hazra and M.
Oestreich,
Copper(I)-Catalyzed Regio- and Chemoselective
Single and Double Addition of Nucleophilic Silicon to Propargylic
Chlorides and Phosphates,
Org. Lett.
2012, 14, 4010-4013 [591]. (Abstract
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123.
M. Mewald and M.
Oestreich,
1,2,3,4-Tetrahydro-1-(1-methylethyl)-1-silanaphthalene,
in Electronic Encyclopedia of Reagents for Organic Synthesis
[595] (Eds.: D. Crich, P. L. Fuchs, A. B. Charette, and T.
Rovis), Wiley, Chichester, 2012. (Abstract
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122.
M. Mewald and M.
Oestreich,
1,2,3,4-Tetrahydro-1-(1,1-dimethylethyl)-1-silanaphthalene,
in Electronic Encyclopedia of Reagents for Organic Synthesis
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Rovis), Wiley, Chichester, 2012. (Abstract
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121.
A. Weickgenannt and
M. Oestreich,
The Renaissance of Silicon-Stereogenic
Silanes: A Personal Account,
in Asymmetric Synthesis -
More Methods and Applications [601] (Eds.: M. Christmann and S.
Bräse), Wiley-VCH, Weinheim, 2012, 35-42.
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120.
C. D. F. Königs, H. F.
T. Klare, Y. Ohki, K. Tatsumi, and M. Oestreich,
Base-Free
Dehydrogenative Coupling of Enolizable Carbonyl Compounds with
Silanes,
Org. Lett. 2012,
14, 2842-2845 [603]. (Abstract [604])
Included into
Organic Chemistry Highlights under www.organic-chemistry.org
[605].
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119.
E. Hartmann and M.
Oestreich,
Two-Directional Desymmetrization by Double
1,4-Addition of Silicon and Boron Nucleophiles,
Org. Lett. 2012, 14,
2406-2409 [607]. (Abstract [608])
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118.
M. Oestreich,
Organic Reactions, Volume 75 (Diamond Volume). Edited by Scott E.
Denmark. Wiley, Hoboken 2012 (Book Review),
Angew.
Chem. 2012, 124, 4344;
Angew.
Chem. Int. Ed. 2012, 51, 4270
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117.
A. Weickgenannt, J. Mohr,
and M. Oestreich,
Catalytic enantioselective dehydrogenative
Si-O coupling of oxime ether-functionalized alcohols
(Tetrahedron Symposium-in-Print "New Trends in
Enantioselective Catalysis with Copper(I)"),
Tetrahedron 2012, 68, 3468-3479
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116.
R. K. Schmidt, K.
Müther, C. Mück-Lichtenfeld, S. Grimme, and M. Oestreich,
Silylium Ion-Catalyzed Challenging Diels-Alder Reactions: The
Danger of Hidden Proton Catalysis with Strong Lewis Acids,
J. Am. Chem. Soc. 2012, 134,
4421-4428 [616]. (Abstract [617])
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115.
M. Mewald, J. A.
Schiffner, and M. Oestreich,
A New
Direction in C-H Alkenylation: Silanol as a Helping Hand
(Highlight),
Angew. Chem. 2012,
124, 1797-1799;
Angew. Chem. Int. Ed.
2012, 51, 1763-1765 [619]. (Abstract
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114.
S. R. Kandukuri, J.
A. Schiffner, and M. Oestreich,
Aerobic
Palladium(II)-Catalyzed 5-endo-trig Cyclization: An Entry into the
Diastereoselective C-2 Alkenylation of Indoles with Tri- and
Tetrasubstituted Double Bonds,
Angew. Chem.
2012, 124, 1291-1295;
Angew. Chem.
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113.
C. Kleeberg, E.
Feldmann, E. Hartmann, D. J. Vyas, and M. Oestreich,
Copper-Catalyzed 1,2-Addition of Nucleophilic Silicon to
Aldehydes: Mechanistic Insight and Catalytic Systems,
Chem. Eur. J. 2011, 17, 13538-13543
[625]. (Abstract [626])
[627]
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112.
T. H. Wöste and M.
Oestreich,
BINAP versus BINAP(O) in Asymmetric
Intermolecular Mizoroki-Heck Reactions: Substantial Effects on
Selectivities,
Chem. Eur. J.
2011, 17, 11914-11918 [628]. (Abstract
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111.
A. Weickgenannt and
M. Oestreich,
A New Motif for Lewis Base Catalysis:
Asymmetric Reduction of β-Enamino Esters (Highlight),
ChemCatChem 2011, 3, 1527-1529
[631]. (Abstract [632])
[633]
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110.
D. J. Vyas, C. K.
Hazra, and M. Oestreich,
Copper(I)-Catalyzed Regioselective
Propargylic Substitution Involving Si-B Bond Activation,
Org. Lett. 2011, 13, 4462-4465
[634]. (Abstract [635])
Included into Organic Chemistry
Highlights under www.organic-chemistry.org [636].
[637]
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109.
E. Hartmann and M.
Oestreich,
Si-B Bond Activation in Asymmetric Cu(I) and
Rh(I) Catalysis,
Chemistry TODAY / Chimica OGGI
2011, 29, 34-36 (September/October
issue).
[638]
- © 2011 American Chemical Society
108.
K. Müther, R.
Fröhlich, C. Mück-Lichtenfeld, S. Grimme, and M. Oestreich,
A Unique Transition Metal-Stabilized Silicon Cation,
J. Am. Chem. Soc. 2011, 133,
12442-12444 [639]. (Abstract [640])
Highlighted in Nachr.
Chem. 2012, 60, 216-250 [641].
Highlighted in Angew. Chem. Int. Ed. 2012,
51, 4526-4528 [642].
[643]
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107.
M. Mewald, R.
Fröhlich, and M. Oestreich,
An Axially Chiral,
Electron-Deficient Borane: Synthesis, Coordination Chemistry, Lewis
Acidity, and Reactivity,
Chem. Eur. J.
2011, 17, 9406-9414 [644]. (Abstract [645])
[646]
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106.
E. Hartmann, D.
J. Vyas, and M. Oestreich,
Enantioselective formal hydration
of α,β-unsaturated acceptors: Asymmetric conjugate addition of
silicon and boron nucleophiles (Feature Article),
Chem. Commun. 2011, 47, 7917-7932
[647]. (Abstract [648])
[649]
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105.
C. D. F. Königs and M.
Oestreich,
Shortened Synthesis of a Silicon-Stereogenic
Cyclic Silane (Practical Synthetic Procedure),
Synthesis 2011, 2062-2065 [650].
(Abstract [651])
[652]
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104.
D. J. Vyas, R.
Fröhlich, and M. Oestreich,
Activation of the Si-B Linkage:
Copper-Catalyzed Addition of Nucleophilic Silicon to Imines,
Org. Lett. 2011, 13, 2094-2097
[653]. (Abstract [654])
[655]
- © 2011 American Chemical Society
103.
H. F. T. Klare, M.
Oestreich, J.-i. Ito, H. Nishiyama, Y. Ohki, and K. Tatsumi,
Cooperative Catalytic Activation of Si–H Bonds
by a Polar Ru–S Bond: Regioselective
Low-Temperature C–H Silylation of Indoles under
Neutral Conditions by a Friedel–Crafts
Mechanism,
J. Am. Chem. Soc.
2011, 133, 3312-3315 [656]. (Abstract
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[658]
- © 2011 Gesellschaft Deutscher Chemiker
102.
M. Oestreich,
Trendbericht 2010 - Organische Chemie:
Metallfreie Synthesemethoden,
Nachr. Chem.
2011, 59, 264 [659]. (Abstract
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[661]
- © 2011 WILEY-VCH
101.
J. A. Schiffner and
M. Oestreich,
All Carbon-Substituted Quaternary Carbon Atoms
in Oxindoles by an Aerobic Palladium(II)-Catalyzed Ring Closure onto
Tri- and Tetrasubstituted Double Bonds,
Eur. J. Org.
Chem. 2011, 1148-1154 [662]. (Abstract [663])
Selected as EurBest in EurJOC.
[664]
- © The Royal Society of Chemistry 2011
100.
K. Müther and
M. Oestreich,
Self-regeneration of a silylium ion catalyst
in carbonyl reduction,
Chem. Commun.
2011, 47, 334-336 [665]. (Abstract [666])
Part of the "Emerging Investigators" Themed Issue of
Chemical Communications.
Highlighted in Angew. Chem.
Int. Ed. 2012, 51, 4526-4528
[667].
[668]
- © 2010 WILEY-VCH
99.
D. J. Vyas and M.
Oestreich,
Copper-Catalyzed Si-B Bond Activation in
Branched-Selective Allylic Substitution of Linear Allylic
Chlorides,
Angew. Chem. 2010,
122, 8692-8694;
Angew. Chem. Int. Ed.
2010, 49, 8513-8515 [669]. (Abstract
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Editors' Choice: ChemInform. [671]
[672]
- © 2010 American Chemical Society
98.
D. J. Vyas, R.
Fröhlich, and M. Oestreich,
Stereochemical Surprises in the
Lewis Acid-Mediated Allylation of Isatins,
J. Org.
Chem. 2010, 75, 6720-6723 [673].
(Abstract [674])
[675]
- © Georg Thieme Verlag
97.
A. Grajewska and M.
Oestreich,
Base-Catalyzed Dehydrogenative Si-O Coupling with
Dihydrosilanes: Silylene Protection of Diols,
Synlett 2010, 2482-2484 [676]. (Abstract
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[678]
- © 2010 The Royal Society of Chemistry
96.
H. F. T. Klare and
M. Oestreich,
Silylium ions in catalysis (Perspective),
(Special Issue "New Horizon of Organosilicon
Chemistry"),
Dalton Trans. 2010,
39, 9176-9184 [679]. (Abstract [680])
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- © 2010 WILEY-VCH
95.
E. Hartmann and M.
Oestreich,
Asymmetric Conjugate Silyl Transfer in Iterative
Catalytic Sequences: Synthesis of the C7-C16 Fragment of
(+)-Neopeltolide,
Angew. Chem.
2010, 122, 6331-6334;
Angew. Chem.
Int. Ed. 2010, 49, 6195-6198 [682].
(Abstract [683])
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- © Georg Thieme Verlag
94.
F. M. J. Tappe, V. T.
Trepohl, and M. Oestreich,
Transition Metal-Catalyzed C-P
Cross-Coupling Reactions (Review),
Synthesis
2010, 3037-3062 [685]. (Abstract [686])
[687]
- © 2010 Elsevier Ltd.
93.
M. Mewald, A. Weickgenannt,
R. Fröhlich, and M. Oestreich,
Expeditious synthesis of
TADDOL-derived phosphoramidite and phosphonite ligands
(Special Issue dedicated to Professor Henri B. Kagan on the occasion
of his 80th birthday),
Tetrahedron: Asymmetry
2010, 21, 1232-1237 [688]. (Abstract
[689])
[690]
- © The Royal Society of Chemistry 2010
92.
A. Weickgenannt,
M. Mewald, and M. Oestreich,
Asymmetric Si-O coupling of
alcohols (Emerging Area),
Org. Biomol. Chem.
2010, 8, 1497-1504 [691]. (Abstract
[692])
Featured on the Inside Cover of Organic &
Biomolecular Chemistry.
[693]
- © 2010 WILEY-VCH
91.
A. Weickgenannt, M.
Mewald, T. W. T. Muesmann, and M. Oestreich,
Catalytic
Asymmetric Si-O Coupling of Simple Achiral Silanes and Chiral
Donor-Functionalized Alcohols,
Angew. Chem.
2010, 122, 2269-2272;
Angew. Chem.
Int. Ed. 2010, 49, 2223-2226 [694].
(Abstract [695])
Highlighted in SYNFACTS
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[697]
- © 2010 Gesellschaft Deutscher Chemiker
90.
M. Oestreich,
Trendbericht 2009 - Organische Chemie:
Metallfreie Synthesemethoden,
Nachr. Chem.
2010, 58, 278 [698]. (Abstract
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- © 2010 WILEY-VCH
89.
J. A. Schiffner, K.
Müther, and M. Oestreich,
Enantioselective Conjugate
Borylation (Highlight),
Angew. Chem.
2010, 122, 1214-1216;
Angew. Chem.
Int. Ed. 2010, 49, 1194-1196 [701].
(Abstract [702])
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- © The Royal Society of Chemistry 2010
88.
D. J. Vyas and M.
Oestreich,
Expedient access to branched allylic silanes by
copper-catalysed allylic substitution of linear allylic
halides,
Chem. Commun.
2010, 46, 568-570 [704]. (Abstract [705])
Selected a "Hot Article" by Chemical
Communications.
[706]
- © 2010 WILEY-VCH
87.
A. Weickgenannt and M.
Oestreich,
Silicon- and Tin-Based Cuprates: Now Catalytic in
Copper! (Concept),
Chem. Eur. J.
2010, 16, 402-412 [707]. (Abstract [708])
Editors' Choice: Spotlights.
[709]
- © 2010 WILEY-VCH
86.
J. A. Schiffner, T. H.
Wöste, and M. Oestreich,
Enantioselective Fujiwara-Moritani
Indole and Pyrrole Annulations Catalyzed by Chiral Palladium(II)-NicOx
Complexes,
Eur. J. Org. Chem.
2010, 174-182 [710]. (Abstract [711])
[712]
- © 2009 WILEY-VCH
85.
H. F. T. Klare, K.
Bergander, and M. Oestreich,
Taming the Silylium Ion for
Low-Temperature Diels–Alder Reactions,
Angew. Chem. 2009, 121, 9241-9243;
Angew. Chem. Int. Ed. 2009,
48, 9077-9079 [713]. (Abstract [714])
Highlighted in
Nachr. Chem. 2010, 58, 7 [715].
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51, 4526-4528 [716].
[717]
- © 2009 WILEY-VCH
84.
D. T. Hog and M.
Oestreich,
B(C6F5)3-Catalyzed Reduction of
Ketones and Imines Using Silicon-Stereogenic Silanes: Stereoinduction
by Single-Point Binding,
Eur. J. Org. Chem.
2009, 5047-5056 [718]. (Abstract [719])
Editors' Choice: Spotlights.
[720]
- © The Royal Society of Chemistry 2009
83.
A. Steves and M.
Oestreich,
Facile preparation of CF3-substituted
carbinols with an azine donor and subsequent kinetic resolution
through stereoselective Si-O coupling,
Org. Biomol.
Chem. 2009, 7, 4464-4469 [721].
(Abstract [722])
[723]
- © 2009 Elsevier Ltd.
82.
V. T. Trepohl, R.
Fröhlich, and M. Oestreich,
Conjugate phosphination of
cyclic and acyclic acceptors using Rh(I)-phosphine and Rh(I)-carbene
complexes. Probing the mechanism with chirality at the silicon atom or
the phosphorus atom of the Si-P reagent
(Tetrahedron
Symposium-in-Print "2008 Tetrahedron Prize for Creativity in
Organic Chemistry to Larry E. Overman"),
Tetrahedron 2009, 65, 6510-6518
[724]. (Abstract [725])
[726]
- © 2009 Elsevier Ltd.
81.
C. Walter, R. Fröhlich,
and M. Oestreich,
Rhodium(I)-catalyzed enantioselective
1,4-addition of nucleophilic silicon
(Tetrahedron
Symposium-in-Print "Recent Advances in Organosilicon
Chemistry Directed towards Organic Synthesis"),
Tetrahedron 2009, 65, 5513-5520
[727]. (Abstract [728])
[729]
- © 2009 WILEY-VCH
80.
E. S. Schmidtmann and
M. Oestreich,
Enantiospecific Preparation and Allylation
Chemistry of All-Carbon-Substituted α-Chiral Allylic
Stannanes,
Angew. Chem. 2009,
121, 4705-4709;
Angew. Chem. Int. Ed.
2009, 48, 4634-4638 [730]. (Abstract
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Highlighted in SYNFACTS 2009,
1002 [732].
[733]
- © 2009 WILEY-VCH
79.
H. F. T. Klare and M.
Oestreich,
Asymmetric Ring-Closing Metathesis with a
Twist (Highlight),
Angew. Chem.
2009, 121, 2119-2123;
Angew. Chem.
Int. Ed. 2009, 48, 2085-2089 [734].
(Abstract [735])
[736]
- © 2009 Gesellschaft Deutscher Chemiker
78.
M. Oestreich,
Trendbericht 2008 - Organische Chemie:
Metallfreie Synthesemethoden,
Nachr. Chem.
2009, 57, 259 [737]. (Abstract
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[739]
- © 2009 American Chemical Society
77.
V. T. Trepohl, S. Mori,
K. Itami, and M. Oestreich,
Palladium(II)-Catalyzed
Conjugate Phosphination of Electron-Deficient Acceptors,
Org. Lett. 2009, 11, 1091-1094
[740]. (Abstract [741])
Included into Organic Chemistry
Highlights under www.organic-chemistry.org [742].
[743]
- © 2009 John Wiley & Sons
76.
M. Oestreich (Editor),
The Mizoroki-Heck Reaction [744], Wiley, Chichester,
2009 (608 pages, Hardcover).
ISBN:
978-0-470-03394-4.
Book Review: Angew. Chem.
2009, 121, 7081 [745]; Angew. Chem. Int.
Ed. 2009, 48, 6947. [746]
Buchbesprechung: Nachr. Chem. 2009,
57, 1030-1031.
Book Review: Synthesis
2010, 718 [747].
Book Review: Org. Process
Res. Dev. 2010, 14, 748 [748].
Book Review: Appl. Organometal. Chem. 2010,
24, 490 [749].
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75.
A. B. Machotta and M.
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Intramolecular Heck Reaction - Formation of
Carbocycles,
in The Mizoroki-Heck Reaction [751]
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179-213.
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- © 2009 WILEY-VCH
74.
A. Weickgenannt and M.
Oestreich,
Potassium tert-Butoxide-Catalyzed
Dehydrogenative Si-O Coupling: Reactivity Pattern and Mechanism of an
Underappreciated Alcohol Protection,
Chem. Asian
J. 2009, 4, 406-410 [753]. (Abstract
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- © 2009 John Wiley & Sons
73.
V. T. Trepohl and
M. Oestreich,
Palladium-Catalyzed Arylation Reactions of
Alkenes (Mizoroki-Heck Reaction and Related Processes),
in
Modern Arylation Methods [756] (Ed.: L. Ackermann),
Wiley-VCH, Weinheim, 2009, 221-269.
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- © 2008 WILEY-VCH
72.
S. Rendler, O. Plefka,
B. Karatas, G. Auer, R. Fröhlich, C. Mück-Lichtenfeld, S. Grimme,
and M. Oestreich,
Stereoselective Alcohol Silylation by
Dehydrogenative Si-O Coupling: Scope, Limitations, and Mechanism of
the Cu-H-Catalyzed Non-Enzymatic Kinetic Resolution with
Silicon-Stereogenic Silanes,
Chem. Eur. J.
2008, 14, 11512-11528 [758]. (Abstract
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- © Springer
71.
R. Brückner, H.-D. Beckhaus, S.
Braukmüller, J. Dirksen, D. Goeppel und M. Oestreich,
Praktikum Präparative Organische Chemie - Organisch-Chemisches
Fortgeschrittenenpraktikum [761],
Spektrum Akademischer
Verlag, Heidelberg, 2009 (374 Seiten, 424
Abbildungen, Softcover) (published in 2008).
ISBN:
978-3-8274-1981-1.
[762]
- © Georg Thieme Verlag
70.
J. A. Schiffner, A. B.
Machotta, and M. Oestreich,
A Catalytic Asymmetric
Fujiwara-Moritani Cyclization,
Synlett
2008, 2271-2274 [763]. (Abstract [764])
[765]
- © WILEY-VCH
69.
S. Rendler and M. Oestreich,
Conclusive Evidence for an SN2-Si Mechanism in the
B(C6F5)3-Catalyzed Carbonyl Hydrosilylation: Implications for the
Related Hydrogenation,
Angew. Chem.
2008, 120, 6086-6089;
Angew. Chem.
Int. Ed. 2008, 47, 5997-6000 [766].
(Abstract [767])
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- © Georg Thieme Verlag
68.
R. K. Schmidt and M.
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Transition Metal-Free Conjugate Stannyl Transfer
to α,β-Unsaturated Carbonyl and Carboxyl Compounds in Basic Aqueous
Media,
Synlett 2008, 1690-1692
[769]. (Abstract [770])
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- © 2008 WILEY-VCH
67.
S. Rendler, R.
Fröhlich, M. Keller, and M. Oestreich,
Enantio- and
Diastereotopos-Differentiation in the Palladium(II)-Catalyzed
Hydrosilylation of Bicyclo[2.2.1]alkene Scaffolds with
Silicon-Stereogenic Silanes,
Eur. J. Org. Chem.
2008, 2582-2591 [772]. (Abstract [773])
Highlighted in SYNFACTS 2008, 855
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66.
C. Walter and M.
Oestreich,
Catalytic Asymmetric C-Si Bond Formation by
Rh(I)-Catalyzed Conjugate Silyl Transfer onto Acyclic
α,β-Unsaturated Acceptors Using the Si-B Interelement
Linkage,
Angew. Chem. 2008,
120, 3878-3880;
Angew. Chem. Int. Ed.
2008, 47, 3818-3820 [776]. (Abstract
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Highlighted in SYNFACTS 2008,
739 [778].
[779]
- © 2008 WILEY-VCH
65.
A. B. Machotta and M.
Oestreich,
Asymmetric Synthesis - The Essentials
(Second, Completely Revised Edition). Edited by Mathias Christmann and
Stefan Bräse. Wiley-VCH, Weinheim 2008 (Book
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Synthesis 2008, 1163 [780].
(Abstract [781])
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- © The Royal Society of Chemistry 2008
64.
B. Karatas, S.
Rendler, R. Fröhlich, and M. Oestreich,
Kinetic Resolution
of Donor-Functionalised Tertiary Alcohols by Cu-H-Catalysed
Stereoselective Silylation Using a Strained Silicon-Stereogenic
Silane,
Org. Biomol. Chem. 2008,
6, 1435-1440 [783]. (Abstract [784])
[785]
- © Springer
63.
R. Brückner, H.-D. Beckhaus, S.
Braukmüller, J. Dirksen, D. Goeppel und M. Oestreich,
Praktikum Präparative Organische Chemie - Organisch-Chemisches
Grundpraktikum [786],
Spektrum Akademischer Verlag,
Heidelberg, 2008 (394 Seiten, 599 Abbildungen,
Softcover).
ISBN: 978-3-8274-1505-9.
Buchbesprechung:
Angew. Chem. 2008, 120, 8106-8108
[787].
Buchbesprechung: Nachr. Chem.
2008, 56, 931-932 [788].
[789]
- © 2008 Gesellschaft Deutscher Chemiker
62.
M. Oestreich,
Trendbericht 2007 - Organische Chemie:
Metallfreie Synthesemethoden,
Nachr. Chem.
2008, 56, 276 [790]. (Abstract
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- © 2008 WILEY-VCH
61.
S. Rendler and M.
Oestreich,
Diverse Modes of Silane Activation for
Hydrosilylation of Carbonyl Compounds,
in Modern
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- © 2008 WILEY-VCH
60.
S. Rendler and M.
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Kinetic Resolution and Desymmetrization by
Stereoselective Alcohol Silylation (Highlight),
Angew.
Chem. 2008, 120, 254-257;
Angew. Chem. Int. Ed. 2008, 47,
248-250 [795]. (Abstract [796])
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- © 2007 WILEY-VCH
59.
H. F. T. Klare and M.
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Chiral Recognition with Silicon-Stereogenic
Silanes: Remarkable Selectivity Factors in the Kinetic Resolution of
Donor-Functionalized Alcohols,
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2007, 119, 9496-9499;
Angew. Chem.
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(Abstract [799])
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58.
S. Rendler
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Asymmetrische Synthese Hand in Hand: Ein
Erfolgsbericht: Asymmetric Synthesis with Chemical and Biological
Methods. Hrsg. von Dieter Enders und Karl-Erich Jaeger. Wiley-VCH,
Weinheim 2007 (Book Review),
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- © 2007 American Chemical Society
57.
A. B. Machotta, B. F.
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Oxygen Donor-Mediated
Equilibration of Diastereomeric Alkene-Palladium(II) Intermediates in
Enantioselective Desymmetrizing Heck Cyclizations,
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56.
V. T. Trepohl and
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Rhodium(I)-catalyzed Conjugate Phosphination
of Cyclic α,β-Unsaturated Ketones with Silylphoshines as Masked
Phosphinides,
Chem. Commun. 2007,
3300-3302 [807]. (Abstract [808])
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- © Georg Thieme Verlag
55.
M. Oestreich,
Silicon-Stereogenic Silanes in Asymmetric Catalysis
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Synlett 2007, 1629-1643
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54.
M. Oestreich,
Directed
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in Directed Metallation
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53.
A. Zimmermann and M.
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2006 (Book Review),
Synthesis
2007, 957 [815]. (Abstract [816])
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52.
M.
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Trendbericht 2006 - Organische Chemie:
Metallfreie Synthesemethoden,
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2007, 55, 272-273 [818]. (Abstract
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- © Beilstein-Institut
51.
S. Rendler and M. Oestreich,
Conformational Rigidity of Silicon-Stereogenic Silanes in
Asymmetric Catalysis: A Comparative Study,
(Thematic Series
on Contemporary Organosilicon Chemistry),
Beilstein J. Org.
Chem. 2007, 3, 9. [821] (open access)
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- © 2007 American Chemical Society
50.
S. Rendler, M.
Oestreich, C. P. Butts, and G. C. Lloyd-Jones,
Intermolecular Chirality Transfer from Silicon to Carbon:
Interrogation of the Two-Silicon Cycle for Pd-Catalyzed
Hydrosilylation by Stereoisotopochemical Cross-over,
J.
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49.
S. Rendler and M.
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Polishing a Diamond in the Rough:
"Cu-H" Catalysis with Silanes (Minireview),
Angew. Chem. 2007, 119, 504-510;
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46, 498-504 [828]. (Abstract [829])
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48.
M. Oestreich,
Synthesis of Arenecarbaldehydes by C-C Bond Formation of
Ar-CH=O (Product Class 6, Section 25.6.8),
in Science
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47.
M. Oestreich,
Synthesis of Aldehydes by Hydration of Alkynes (Product Class
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in Science of Synthesis, Volume 25
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46.
A. B. Machotta and M.
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Organic Chemistry Online...and for Free?
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45.
E. S. Schmidtmann
and M. Oestreich,
Mechanistic Insight into Copper-Catalysed
Allylic Substitutions with Bis(triorganosilyl) Zincs: Enantiospecific
Preparation of α-Chiral Allylic Silanes,
Chem.
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- © 2006 WILEY-VCH
44.
C. Walter, G. Auer,
and M. Oestreich,
Rhodium-Catalyzed Enantioselective
Conjugate Silyl Transfer: 1,4-Addition of Silyl Boronic Esters to
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