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Inhalt des Dokuments

Publications

  • 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

2018

242.
L. Omann, B. Pudasaini, E. Irran, H. F. T. Klare, M.-H. Baik, and M. Oestreich,
Thermodynamic versus Kinetic Control in Substituent Redistribution Reactions of Silylium Ions Steered by the Counteranion,
submitted for publication.

241.
P. Shaykhutdinova, S. Keess, and M. Oestreich,
Cationic Silicon-Based Lewis Acids in Catalysis,
in Organosilicon Chemistry – Novel Approaches and Reactions (Eds.: T. Hiyama, M. Oestreich), Wiley-VCH, Weinheim, 2018, submitted for publication.

240.
L. Omann, E. Irran, H. F. T. Klare, and M. Oestreich,
Electrophilic Formylation of Arenes by Silylium Ion-Mediated Activation of Carbon Monoxide,
in revision.

239.
F. Forster and M. Oestreich,
Bioinspired Catalytic Generation of Main-Group Electrophiles by Cooperative Bond Activation (Account),
Chimia 2018, 72, submitted for publication.

238.
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. Int. Ed. 2018, 57, early view on April 12, 2018 [1]. (Abstract [2])

236.
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. 2018, early view on April 6, 2018. [3] (Abstract [4])

237.
W. Yuan, P. Smirnov, and M. Oestreich,
Custom Hydrosilane Synthesis Based on Monosilane,
Chem 2018, 4, in press (to appear on April 26, 2018).

235.
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,
Eur. J. Org. Chem. 2018, Accepted Article on March 25, 2018 [5]. (Abstract [6])

Lupe [7]

234.
S. Bähr and M. Oestreich,
A Neutral Ru(II) Hydride Complex for the Regio- and Chemoselective Reduction of N-Silylpyridinium Ions,
Chem. Eur. J. 2018, 24, 5613-5622 [8]. (Abstract [9])

Lupe [10]

233.
S. Bähr and M. Oestreich,
The Electrophilic Aromatic Substitution Approach to C-H Silylation and C-H Borylation
(IMEBORON XVI Conference Issue [11]),
Pure Appl. Chem. 2018, 90, 723-731 [12]. (Abstract [13])

Lupe [14]

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 [15]. (Abstract [16])

2017

Lupe [17]

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 [18]. (Abstract [19])
Highlighted in SYNFACTS 2018, 14, 165 [20].

Lupe [21]

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 [22]. (Abstract [23])

Lupe [24]

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. 2017, 139, 16334-16342 [25]. (Abstract [26])
Featured on the Front Cover of JACS [27].

Lupe [28]

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 Trans. 2017, 46, 16412-16418 [29]. (Abstract)
Featured on the Front Cover of Dalton Transactions [30].

Lupe [31]

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 2017, 36, 4013-4019 [32]. (Abstract [33])

Lupe [34]

226.
S. Wübbolt and M. Oestreich,
Exhaustive Chemoselective Reduction of Nitriles by Catalytic Hydrosilylation Involving Cooperative Si-H Bond Activation
(SYNLETT Cluster on Silicon in Synthesis and Catalysis [35]),
Synlett 2017, 28, 2411-2414 [36]. (Abstract [37])

Preface by M. Oestreich,
Synlett 2017, 28, 2394-2395 [38]. (Abstract [39])

Lupe [40]

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 [41]. (Abstract)

Lupe [42]

224.
W. Xue and M. Oestreich,
Copper-Catalyzed Decarboxylative Radical Silylation of Redox-Active Aliphatic Carboxylic Acid Derivatives,
Angew. Chem. 2017, 129, 11808-11811;
Angew. Chem. Int. Ed. 2017, 56, 11649-11652 [43]. (Abstract [44])

Lupe [45]

223.
D. Porwal and M. Oestreich,
B(C6F5)3-Catalyzed Reduction of Sulfoxides and Sulfones to Sulfides with Hydrosilanes,
Synthesis 2017, 49, 4698-4702 [46]. (Abstract [47])

Lupe [48]

222.
S. Keess and M. Oestreich,
Tri(cyclohexa-2,5-dien-1-yl)silane,
in Electronic Encyclopedia of Reagents for Organic Synthesis [49] (Eds.: D. Crich, P. L. Fuchs, A. B. Charette, and T. Rovis), Wiley, Chichester, 2017.
(Abstract [50])

Lupe [51]

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 Base,
Organometallics 2017, 36, 2381-2384 [52]. (Abstract [53])

Lupe [54]

220.
S. Keess and M. Oestreich,
Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes (Minireview),
Chem. Sci. 2017, 8, 4688-4695 [55]. (Abstract)
(open access)

Lupe [56]

219.
Q. Yin and M. Oestreich,
Photocatalysis Enabling Acceptorless Dehydrogenation of Benzofused Saturated Rings at Room Temperature (Highlight),
Angew. Chem. 2017, 129, 7824-7826;
Angew. Chem. Int. Ed. 2017, 56, 7716-7718 [57]. (Abstract [58])

Lupe [59]

218.
X. Dong, A. Weickgenannt, and M. Oestreich,
Broad-spectrum kinetic resolution of alcohols enabled by Cu–H-catalysed dehydrogenative coupling with hydrosilanes,
Nature Commun. 2017, 8, 15547 [60]. (Abstract)
(open access)

Lupe [61]

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. 2017, 139, 6867-6879 [62]. (Abstract [63])

Lupe [64]

216.
L. Omann, C. D. F. Königs, H. F. T. Klare, and M. Oestreich,
Cooperative Catalysis at MetalSulfur Bonds (Account),
Acc. Chem. Res. 2017, 50, 1258-1269 [65]. (Abstract [66])

Lupe [67]

215.
L.-Y. Jiao and M. Oestreich,
C-H Bond Functionalization at the Benzene Core of Indoles and Indolines (Excluding C-2 and C-3) [68],
in Strategies for Palladium-Catalyzed Non-Directed and Directed C-H Bond Functionalization [69] (Eds.: A. R. Kapdi, D. Maiti), Elsevier, Oxford, 2017, 205-232. (Abstract)

Lupe [70]

214.
P. Pommerening, J. Mohr, J. Friebel, and M. Oestreich,
Synthesis of a Chiral Borate Counteranion, its Trityl Salt, and Application Thereof in Lewis-Acid Catalysis,
Eur. J. Org. Chem. 2017, 2312-2316 [71]. (Abstract [72])

Lupe [73]

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,
[Collaborative Research Center (SFB 858) on Cooperative Effects [74]]
Chem. Eur. J. 2017, 23, 6213-6219 [75]. (Abstract [76])

Lupe [77]

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 [78]]
Chem. Eur. J. 2017, 23, 5925-5928 [79]. (Abstract [80])

Lupe [81]

211.
L. B. Delvos and M. Oestreich,
Silylboron Reagents (Volume 4, Product Class 7, Section 4.4.7),
in Science of Synthesis Knowledge Updates 2017/1 [82] (Ed.: M. Oestreich), Thieme, Stuttgart, 2017, 65-176. (Abstract [83])

Lupe [84]

210.
S. Keess and M. Oestreich,
Access to Fully Alkylated Germanes by B(C6F5)3-Catalyzed Transfer Hydrogermylation of Alkenes,
Org. Lett. 2017, 19, 1898-1901 [85]. (Abstract [86])

Lupe [87]

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;
Angew. Chem. Int. Ed. 2017, 56, 3712-3717 [88]. (Abstract [89])
Highlighted in SYNFACTS 2017, 13, 529 [90].

Lupe [91]

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;
Angew. Chem. Int. Ed. 2017, 56, 3389-3391 [92]. (Abstract [93])

Lupe [94]

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 [95]. (Abstract [96])

Lupe [97]

206.
L. Omann and M. Oestreich,
Catalytic Access to Indole-Fused Benzosiloles by 2-Fold Electrophilic C–H Silylation with Dihydrosilanes,
Organometallics 2017, 36, 767-776 [98]. (Abstract [99])
Featured on the Cover of Organometallics [100].

Lupe [101]

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 [102]. (Abstract [103])

Lupe [104]

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;
Angew. Chem. Int. Ed. 2017, 56, 52-59 [105]. (Abstract [106])

2016

203.
H. F. T. Klare and M. Oestreich,
Teaching nature the unnatural (Perspective),
Science 2016, 354, 970 [107]. (Abstract [108])

Lupe [109]

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. 2016, 138, 14222-14225 [110]. (Abstract [111])

Lupe [112]

201.
J. Mohr and M. Oestreich,
Balancing C=C Functionalization and C=O Reduction in Cu-H Catalysis (Highlight),
Angew. Chem. 2016, 128, 12330-12332;
Angew. Chem. Int. Ed. 2016, 55, 12148-12149 [113]. (Abstract [114])

Lupe [115]

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 [116]. (Abstract [117])

Lupe [118]

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 [119]. (Abstract [120])

Lupe [121]

198.
P. Smirnov and M. Oestreich,
Merging Platinum-Catalyzed Alkene Hydrosilylation with SiH4 Surrogates: Salt-Free Preparation of Trihydrosilanes,
Organometallics 2016, 35, 2433-2434 [122]. (Abstract [123])

Lupe [124]

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 [125]. (Abstract [126])
ACS AuthorChoice (open access)

Lupe [127]

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 [128]. (Abstract [129])

Lupe [130]

195.
I. Chatterjee and M. Oestreich,
Brønsted Acid-Catalyzed Transfer Hydrogenation of Imines and Alkenes Using Cyclohexa-1,4-dienes as Dihydrogen Surrogates,
Org. Lett. 2016, 18, 2463-2466 [131]. (Abstract [132])
ACS AuthorChoice (open access)
Highlighted in SYNFACTS 2016, 12, 971 [133].

Lupe [134]

194.
L. Süsse, J. Hermeke, and M. Oestreich,
The Asymmetric Piers Hydrosilylation,
J. Am. Chem. Soc. 2016, 138, 6940-6943 [135]. (Abstract [136])
ACS AuthorChoice (open access)
Highlighted in SYNFACTS 2016, 12, 833 [137].

Lupe [138]

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. 2016, 22, 10009-10016 [139]. (Abstract [140])

Lupe [141]

192.
C. Fopp, E. Romain, K. Isaac, F. Chemla, F. Ferreira, O. Jackowski, M. Oestreich, and A. Perez-Luna,
Stereodivergent Silylzincation of α-Heteroatom-Substituted Alkynes,
Org. Lett. 2016, 18, 2054-2057 [142]. (Abstract [143])
Highlighted in SYNFACTS 2016, 12, 729 [144].

Lupe [145]

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 [146]. (Abstract [147])

Lupe [148]

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 [149]. (Abstract [150])
ACS AuthorChoice (open access)

Lupe [151]

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 [152]. (Abstract [153])

Lupe [154]

188.
A. Hensel and M. Oestreich,
Asymmetric Addition of Boron and Silicon Nucleophiles [155],
in Progress in Enantioselective Cu(I)-catalyzed Formation of Stereogenic Centers (Ed.: S. R. Harutyunyan), Springer International Publishing Switzerland,
Top. Organomet. Chem. 2016, 58, 135-167.

Lupe [156]

187.
A. Simonneau and M. Oestreich,
3-(Trimethylsilyl)-1,4-cyclohexadiene,
in Electronic Encyclopedia of Reagents for Organic Synthesis [157] (Eds.: D. Crich, P. L. Fuchs, A. B. Charette, and T. Rovis), Wiley, Chichester, 2016. (Abstract [158])

Lupe [159]

186.
R. K. Schmidt, H. F. T. Klare, R. Fröhlich, and M. Oestreich,
Planar Chiral, Ferrocene-Stabilized Silicon Cations,
Chem. Eur. J. 2016, 22, 5376-5383 [160]. (Abstract [161])

Lupe [162]

185.
Q. Yin, H. F. T. Klare, and M. Oestreich,
FriedelCrafts-Type Intermolecular CH Silylation of Electron-Rich Arenes Initiated by Base-Metal Salts,
Angew. Chem. 2016, 128, 3256-3260;
Angew. Chem. Int. Ed. 2016, 55, 3204-3207 [163]. (Abstract [164])

Lupe [165]

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, 11, 367-370 [166]. (Abstract [167])

Lupe [168]

183.
M. Oestreich,
Transfer Hydrosilylation (Minireview),
Angew. Chem. 2016, 128, 504-509;
Angew. Chem. Int. Ed. 2016, 55, 494-499 [169]. (Abstract [170])
(open access)

2015

Lupe [171]

182.
S. Wübbolt and M. Oestreich,
Catalytic Electrophilic C-H Silylation of Pyridines Enabled by Temporary Dearomatization,
Angew. Chem. 2015, 127, 16103-16106;
Angew. Chem. Int. Ed. 2015, 54, 15876-15879 [172]. (Abstract [173])

Lupe [174]

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 and Hydrazones,
Chem. Eur. J. 2015, 21, 17583-17586 [175]. (Abstract [176])

Lupe [177]

180.
T. T. Metsänen, D. Gallego, T. Szilvási, M. Driess, and M. Oestreich,
Peripheral mechanism of a carbonyl hydrosilylation catalyzed by an SiNSi iron pincer complex,
Chem. Sci. 2015, 6, 7143-7149 [178]. (Abstract)
(open access)

Lupe [179]

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 [180]. (Abstract [181])
Highlighted as a "Very Important Paper (VIP)" by Angewandte Chemie.
Featured on the Back Cover of Angewandte Chemie [182].

Lupe [183]

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 [184]. (Abstract [185])

Lupe [186]

177.
A. Simonneau, T. Biberger, and M. Oestreich,
The Cyclohexadienyl-Leaving-Group Approach toward Donor-Stabilized Silylium Ions,
Organometallics 2015, 34, 3927-3929 [187]. (Abstract [188])
ACS AuthorChoice (open access)

Lupe [189]

176.
A. Simonneau and M. Oestreich,
Formal SiH4 chemistry using stable and easy-to-handle surrogates,
Nature Chem. 2015, 7, 816-822 [190]. (Abstract [191])
Highlighted in SYNFACTS 2015, 11, 1158 [192].
Highlighted in Nachr. Chem. 2016, 64, 6.

Lupe [193]

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 [194]. (Abstract [195])

Lupe [196]

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 [197]. (Abstract [198])
ACS AuthorChoice (open access)

Lupe [199]

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 SiH bond activation at RuS bonds,
Chem. Sci. 2015, 6, 4324-4334 [200]. (Abstract)
(open access)

Lupe [201]

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 [202]. (Abstract [203])
Highlighted in SYNFACTS 2015, 11, 829 [204].

Lupe [205]

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 [206]. (Abstract [207])
ACS AuthorChoice (open access)
Highlighted to SYNFACTS 2015, 11, 855 [208].

Lupe [209]

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 [210]. (Abstract [211])

Lupe [212]

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 [213]. (Abstract [214])

Lupe [215]

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 [216]. (Abstract [217])

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).

Lupe [218]

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 [219]. (Abstract [220])
ACS AuthorChoice (open access)

Lupe [221]

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 [222]. (Abstract)
(open access)

Lupe [223]

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 [224]. (Abstract [225])
Featured on the Cover of Organometallics [226].

Lupe [227]

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 [228]. (Abstract [229])

2014

Lupe [230]

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 [231]. (Abstract [232])

Lupe [233]

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 [234]. (Abstract [235])

Lupe [236]

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 [237]. (Abstract [238])

Lupe [239]

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 [240]. (Abstract [241])
Highlighted in SYNFACTS 2015, 11, 79 [242].

Lupe [243]

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 [244]. (Abstract [245])

Lupe [246]

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 [247]. (Abstract [248])

Lupe [249]

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 [250]. (Abstract [251])

Lupe [252]

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 [253]. (Abstract [254])

Lupe [255]

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 [256]. (Abstract [257])
Highlighted in ChemCatChem 2014, 6, 2486-2489 [258].

Lupe [259]

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 [260]),
Chem. Eur. J. 2014, 20, 9250-9254 [261]. (Abstract [262])

Editorial by M. Driess and M. Oestreich,
Chem. Eur. J. 2014, 20, 9144-9145 [263]. (Abstract [264])

Lupe [265]

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 [266]. (Abstract [267])
Highlighted in SYNFACTS 2014, 10, 840 [268].

Lupe [269]

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 [270]. (Abstract [271])

Lupe [272]

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 [273]. (Abstract [274])

Lupe [275]

149.
U. Hennecke, C. Rösner, T. Wald, T. Robert, and M. Oestreich,
Addition Reactions with Formation of Carbon-Halogen Bonds [276],
in Comprehensive Organic Synthesis II (Eds.: G. Molander and P. Knochel), Elsevier, Oxford, 2014, Vol. 7, 638-691 (Abstract [277]).

Lupe [278]

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 [279]. (Abstract [280])

Lupe [281]

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 [282]. (Abstract [283])

Lupe [284]

146.
A. de Meijere, S. Bräse, and M. Oestreich (Editors),
Metal-Catalyzed Cross-Coupling Reactions and More [285], Wiley-VCH, Weinheim, 2014 (1576 pages, Hardcover).
ISBN: 978-3-527-33154-3.
Book Review: Angew. Chem. 2014, 126, 13215-13216 [286]; Angew. Chem. Int. Ed. 2014, 53, 13001-13002 [287].

Lupe [288]

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 [289]. (Abstract [290])

2013

Lupe [291]

144.
L.-Y. Jiao and M. Oestreich,
Oxidative Palladium(II)-Catalyzed C-7 Alkenylation of Indolines,
Org. Lett. 2013, 15, 5374-5377 [292]. (Abstract [293])

Lupe [294]

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 [295]. (Abstract [296])

Lupe [297]

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 [298] (September/October issue).

Lupe [299]

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 [300]. (Abstract [301])
Highlighted as a "Very Important Paper (VIP)" by Chemistry - A European Journal.

Lupe [302]

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 [303]. (Abstract [304])
Highlighted in SYNFACTS 2014, 10, 73 [305].

Lupe [306]

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 [307]. (Abstract [308])
Highlighted in SYNFACTS 2013, 9, 1216 [309].

Lupe [310]

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 [311]. (Abstract [312])
Selected as a "Hot Paper" by Angewandte Chemie.

Lupe [313]

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 [314]. (Abstract [315])

Lupe [316]

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 [317]. (Abstract [318])

Lupe [319]

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 [320]. (Abstract [321])
Featured on the Cover of ACS Catalysis [322].

Lupe [323]

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 [324]. (Abstract [325])

Lupe [326]

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 [327]. (Abstract [328])

Lupe [329]

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 [330]. (Abstract [331])
Highlighted in SYNFACTS 2013, 9, 744 [332].

Lupe [333]

131.
C. D. F. Königs, M. F. Müller, N. Aiguabella, H. F. T. Klare, and M. Oestreich,
Catalytic dehydrogenative SiN coupling of pyrroles, indoles, carbazoles as well as anilines with hydrosilanes without added base,
Chem. Commun. 2013, 49, 1506-1508 [334]. (Abstract [335])

Lupe [336]

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 RuS Dimer in the Catalytic Cycle,
J. Am. Chem. Soc. 2013, 135, 1248-1251 [337]. (Abstract [338])

Lupe [339]

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 [340]. (Abstract [341])

2012

Lupe [342]

128.
W. Nie, H. F. T. Klare, M. Oestreich, R. Fröhlich, G. Kehr, and G. Erker,
Reversible Heterolytic SiH Bond Activation by an Intramolecular Frustrated Lewis Pair
(Special Issue dedicated to Professor Heribert Offermanns),
Z. Naturforsch. 2012, 67b, 987-994 [343]. (Abstract [344])

Lupe [345]

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 [346]. (Abstract [347])

Lupe [348]

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 [349]. (Abstract [350])

Lupe [351]

125.
T. H. Wöste and M. Oestreich,
Hemilabile BINAP(O) as a Chiral Ligand in Desymmetrizing Mizoroki-Heck Cyclizations,
ChemCatChem 2012, 4, 2096-2101 [352]. (Abstract [353])
Highlighted in ChemViews Magazine [354].

Lupe [355]

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 [356]. (Abstract [357])
Highlighted in SYNFACTS 2012, 8, 1239 [358].

Lupe [359]

123.
M. Mewald and M. Oestreich,
1,2,3,4-Tetrahydro-1-(1-methylethyl)-1-silanaphthalene,
in Electronic Encyclopedia of Reagents for Organic Synthesis [360] (Eds.: D. Crich, P. L. Fuchs, A. B. Charette, and T. Rovis), Wiley, Chichester, 2012. (Abstract [361])

Lupe [362]

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 [363] (Eds.: D. Crich, P. L. Fuchs, A. B. Charette, and T. Rovis), Wiley, Chichester, 2012. (Abstract [364])

Lupe [365]

121.
A. Weickgenannt and M. Oestreich,
The Renaissance of Silicon-Stereogenic Silanes: A Personal Account,
in Asymmetric Synthesis - More Methods and Applications [366] (Eds.: M. Christmann and S. Bräse), Wiley-VCH, Weinheim, 2012, 35-42.

Lupe [367]

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 [368]. (Abstract [369])
Included into Organic Chemistry Highlights under www.organic-chemistry.org [370].

Lupe [371]

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 [372]. (Abstract [373])

Lupe [374]

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 [375]. (Abstract [376])

Lupe [377]

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 [378]. (Abstract [379])

Lupe [380]

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 [381]. (Abstract [382])

Lupe [383]

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 [384]. (Abstract [385])

Lupe [386]

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. Int. Ed. 2012, 51, 1265-1269 [387]. (Abstract [388])

2011

Lupe [389]

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 [390]. (Abstract [391])

Lupe [392]

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 [393]. (Abstract [394])

Lupe [395]

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 [396]. (Abstract [397])

Lupe [398]

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 [399]. (Abstract [400])
Included into Organic Chemistry Highlights under www.organic-chemistry.org [401].

Lupe [402]

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).

Lupe [403]

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 [404]. (Abstract [405])
Highlighted in Nachr. Chem. 2012, 60, 216-250 [406].
Highlighted in Angew. Chem. Int. Ed. 2012, 51, 4526-4528 [407].

Lupe [408]

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 [409]. (Abstract [410])

Lupe [411]

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 [412]. (Abstract [413])

Lupe [414]

105.
C. D. F. Königs and M. Oestreich,
Shortened Synthesis of a Silicon-Stereogenic Cyclic Silane (Practical Synthetic Procedure),
Synthesis 2011, 2062-2065 [415]. (Abstract [416])

Lupe [417]

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 [418]. (Abstract [419])

Lupe [420]

103.
H. F. T. Klare, M. Oestreich, J.-i. Ito, H. Nishiyama, Y. Ohki, and K. Tatsumi,
Cooperative Catalytic Activation of SiH Bonds by a Polar RuS Bond: Regioselective Low-Temperature CH Silylation of Indoles under Neutral Conditions by a FriedelCrafts Mechanism,
J. Am. Chem. Soc. 2011, 133, 3312-3315 [421]. (Abstract [422])

Lupe [423]

102.
M. Oestreich,
Trendbericht 2010 - Organische Chemie: Metallfreie Synthesemethoden,
Nachr. Chem. 2011, 59, 264 [424]. (Abstract [425])

Lupe [426]

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 [427]. (Abstract [428])
Selected as EurBest in EurJOC.

Lupe [429]

100.
K. Müther and M. Oestreich,
Self-regeneration of a silylium ion catalyst in carbonyl reduction,
Chem. Commun. 2011, 47, 334-336 [430]. (Abstract [431])
Part of the "Emerging Investigators" Themed Issue of Chemical Communications.
Highlighted in Angew. Chem. Int. Ed. 2012, 51, 4526-4528 [432].

2010

Lupe [433]

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 [434]. (Abstract [435])
Editors' Choice: ChemInform. [436]

Lupe [437]

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 [438]. (Abstract [439])

Lupe [440]

97.
A. Grajewska and M. Oestreich,
Base-Catalyzed Dehydrogenative Si-O Coupling with Dihydrosilanes: Silylene Protection of Diols,
Synlett 2010, 2482-2484 [441]. (Abstract [442])

Lupe [443]

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 [444]. (Abstract [445])

Lupe [446]

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 [447]. (Abstract [448])

Lupe [449]

94.
F. M. J. Tappe, V. T. Trepohl, and M. Oestreich,
Transition Metal-Catalyzed C-P Cross-Coupling Reactions (Review),
Synthesis 2010, 3037-3062 [450]. (Abstract [451])

Lupe [452]

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 [453]. (Abstract [454])

Lupe [455]

92.
A. Weickgenannt, M. Mewald, and M. Oestreich,
Asymmetric Si-O coupling of alcohols (Emerging Area),
Org. Biomol. Chem. 2010, 8, 1497-1504 [456]. (Abstract [457])
Featured on the Inside Cover of Organic & Biomolecular Chemistry.

Lupe [458]

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 [459]. (Abstract [460])
Highlighted in SYNFACTS 2010, 549 [461].

Lupe [462]

90.
M. Oestreich,
Trendbericht 2009 - Organische Chemie: Metallfreie Synthesemethoden,
Nachr. Chem. 2010, 58, 278 [463]. (Abstract [464])

Lupe [465]

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 [466]. (Abstract [467])

Lupe [468]

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 [469]. (Abstract [470])
Selected a "Hot Article" by Chemical Communications.

Lupe [471]

87.
A. Weickgenannt and M. Oestreich,
Silicon- and Tin-Based Cuprates: Now Catalytic in Copper! (Concept),
Chem. Eur. J. 2010, 16, 402-412 [472]. (Abstract [473])
Editors' Choice: Spotlights.

Lupe [474]

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 [475]. (Abstract [476])

2009

Lupe [477]

85.
H. F. T. Klare, K. Bergander, and M. Oestreich,
Taming the Silylium Ion for Low-Temperature DielsAlder Reactions,
Angew. Chem. 2009, 121, 9241-9243;
Angew. Chem. Int. Ed. 2009, 48, 9077-9079 [478]. (Abstract [479])
Highlighted in Nachr. Chem. 2010, 58, 7 [480].
Highlighted in Angew. Chem. Int. Ed. 2012, 51, 4526-4528 [481].

Lupe [482]

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 [483]. (Abstract [484])
Editors' Choice: Spotlights.

Lupe [485]

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 [486]. (Abstract [487])

Lupe [488]

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 [489]. (Abstract [490])

Lupe [491]

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 [492]. (Abstract [493])

Lupe [494]

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 [495]. (Abstract [496])
Highlighted in SYNFACTS 2009, 1002 [497].

Lupe [498]

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 [499]. (Abstract [500])

Lupe [501]

78.
M. Oestreich,
Trendbericht 2008 - Organische Chemie: Metallfreie Synthesemethoden,
Nachr. Chem. 2009, 57, 259 [502]. (Abstract [503])

Lupe [504]

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 [505]. (Abstract [506])
Included into Organic Chemistry Highlights under www.organic-chemistry.org [507].

Lupe [508]

76.
M. Oestreich (Editor),
The Mizoroki-Heck Reaction [509], Wiley, Chichester, 2009 (608 pages, Hardcover).
ISBN: 978-0-470-03394-4.
Book Review: Angew. Chem. 2009, 121, 7081 [510]; Angew. Chem. Int. Ed. 2009, 48, 6947. [511]
Buchbesprechung: Nachr. Chem. 2009, 57, 1030-1031.
Book Review: Synthesis 2010, 718 [512].
Book Review: Org. Process Res. Dev. 2010, 14, 748 [513].
Book Review: Appl. Organometal. Chem. 2010, 24, 490 [514].

Lupe [515]

75.
A. B. Machotta and M. Oestreich,
Intramolecular Heck Reaction - Formation of Carbocycles,
in The Mizoroki-Heck Reaction [516] (Ed.: M. Oestreich), Wiley, Chichester, 2009, 179-213.

Lupe [517]

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 [518]. (Abstract [519])

Lupe [520]

73.
V. T. Trepohl and M. Oestreich,
Palladium-Catalyzed Arylation Reactions of Alkenes (Mizoroki-Heck Reaction and Related Processes),
in Modern Arylation Methods [521] (Ed.: L. Ackermann), Wiley-VCH, Weinheim, 2009, 221-269.

2008

Lupe [522]

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 [523]. (Abstract [524])

Lupe [525]

71.
R. Brückner, H.-D. Beckhaus, S. Braukmüller, J. Dirksen, D. Goeppel und M. Oestreich,
Praktikum Präparative Organische Chemie - Organisch-Chemisches Fortgeschrittenenpraktikum [526],
Spektrum Akademischer Verlag, Heidelberg, 2009 (374 Seiten, 424 Abbildungen, Softcover) (published in 2008).
ISBN: 978-3-8274-1981-1.

Lupe [527]

70.
J. A. Schiffner, A. B. Machotta, and M. Oestreich,
A Catalytic Asymmetric Fujiwara-Moritani Cyclization,
Synlett 2008, 2271-2274 [528]. (Abstract [529])

Lupe [530]

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 [531]. (Abstract [532])

Lupe [533]

68.
R. K. Schmidt and M. Oestreich,
Transition Metal-Free Conjugate Stannyl Transfer to α,β-Unsaturated Carbonyl and Carboxyl Compounds in Basic Aqueous Media,
Synlett 2008, 1690-1692 [534]. (Abstract [535])

Lupe [536]

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 [537]. (Abstract [538])
Highlighted in SYNFACTS 2008, 855 [539].

Lupe [540]

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 [541]. (Abstract [542])
Highlighted in SYNFACTS 2008, 739 [543].

Lupe [544]

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 Review),
Synthesis 2008, 1163 [545]. (Abstract [546])

Lupe [547]

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 [548]. (Abstract [549])

Lupe [550]

63.
R. Brückner, H.-D. Beckhaus, S. Braukmüller, J. Dirksen, D. Goeppel und M. Oestreich,
Praktikum Präparative Organische Chemie - Organisch-Chemisches Grundpraktikum [551],
Spektrum Akademischer Verlag, Heidelberg, 2008 (394 Seiten, 599 Abbildungen, Softcover).
ISBN: 978-3-8274-1505-9.
Buchbesprechung: Angew. Chem. 2008, 120, 8106-8108 [552].
Buchbesprechung: Nachr. Chem. 2008, 56, 931-932 [553].

Lupe [554]

62.
M. Oestreich,
Trendbericht 2007 - Organische Chemie: Metallfreie Synthesemethoden,
Nachr. Chem. 2008, 56, 276 [555]. (Abstract [556])

Lupe [557]

61.
S. Rendler and M. Oestreich,
Diverse Modes of Silane Activation for Hydrosilylation of Carbonyl Compounds,
in Modern Reduction Methods [558] (Eds.: P. G. Andersson and I. J. Munslow), Wiley-VCH, Weinheim, 2008, 183-207.

Lupe [559]

60.
S. Rendler and M. Oestreich,
Kinetic Resolution and Desymmetrization by Stereoselective Alcohol Silylation (Highlight),
Angew. Chem. 2008, 120, 254-257;
Angew. Chem. Int. Ed. 2008, 47, 248-250 [560]. (Abstract [561])

2007

Lupe [562]

59.
H. F. T. Klare and M. Oestreich,
Chiral Recognition with Silicon-Stereogenic Silanes: Remarkable Selectivity Factors in the Kinetic Resolution of Donor-Functionalized Alcohols,
Angew. Chem. 2007, 119, 9496-9499;
Angew. Chem. Int. Ed. 2007, 46, 9335-9338 [563]. (Abstract [564])

Lupe [565]

58.
S. Rendler and M. Oestreich,
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),
Nachr. Chem. 2007, 55, 1032-1033 [566]. (Abstract [567])

Lupe [568]

57.
A. B. Machotta, B. F. Straub, and M. Oestreich,
Oxygen Donor-Mediated Equilibration of Diastereomeric Alkene-Palladium(II) Intermediates in Enantioselective Desymmetrizing Heck Cyclizations,
J. Am. Chem. Soc. 2007, 129, 13455-13463 [569]. (Abstract [570])

Lupe [571]

56.
V. T. Trepohl and M. Oestreich,
Rhodium(I)-catalyzed Conjugate Phosphination of Cyclic α,β-Unsaturated Ketones with Silylphoshines as Masked Phosphinides,
Chem. Commun. 2007, 3300-3302 [572]. (Abstract [573])

Lupe [574]

55.
M. Oestreich,
Silicon-Stereogenic Silanes in Asymmetric Catalysis (Account),
Synlett 2007, 1629-1643 [575]. (Abstract [576])

Lupe [577]

54.
M. Oestreich,
Directed Mizoroki-Heck Reactions [578],
in Directed Metallation (Ed.: N. Chatani), Springer, Heidelberg,
Top. Organomet. Chem.
2007, 24, 169-192.

Lupe [579]

53.
A. Zimmermann and M. Oestreich,
Asymmetric Synthesis - The Essentials. Edited by Mathias Christmann and Stefan Bräse. Wiley-VCH, Weinheim, 2006 (Book Review),
Synthesis 2007, 957 [580]. (Abstract [581])

Lupe [582]

52.
M. Oestreich,
Trendbericht 2006 - Organische Chemie: Metallfreie Synthesemethoden,
Nachr. Chem. 2007, 55, 272-273 [583]. (Abstract [584])

Lupe [585]

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. [586] (open access) (Abstract [587])

Lupe [588]

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. Am. Chem. Soc. 2007, 129, 502-503 [589]. (Abstract [590])
Highlighted in SYNFACTS 2007, 409. [591]

Lupe [592]

49.
S. Rendler and M. Oestreich,
Polishing a Diamond in the Rough: "Cu-H" Catalysis with Silanes (Minireview),
Angew. Chem. 2007, 119, 504-510;
Angew. Chem. Int. Ed. 2007, 46, 498-504 [593]. (Abstract [594])

2006

Lupe [595]

48.
M. Oestreich,
Synthesis of Arenecarbaldehydes by C-C Bond Formation of Ar-CH=O (Product Class 6, Section 25.6.8),
in Science of Synthesis, Volume 25 (Ed.: R. Brückner), Thieme, Stuttgart, 2006, pp 667-688.

Lupe [596]

47.
M. Oestreich,
Synthesis of Aldehydes by Hydration of Alkynes (Product Class 1, Section 25.1.8),
in Science of Synthesis, Volume 25 (Ed.: R. Brückner), Thieme, Stuttgart, 2006, pp 199-211.

Lupe [597]

46.
A. B. Machotta and M. Oestreich,
Organic Chemistry Online...and for Free? (Website Review),
Angew. Chem. 2006, 118, 7272;
Angew. Chem. Int. Ed. 2006, 45, 7114 [598]. (Abstract [599])

Lupe [600]

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. Commun. 2006, 3643-3645 [601]. (Abstract [602])

Lupe [603]

44.
C. Walter, G. Auer, and M. Oestreich,
Rhodium-Catalyzed Enantioselective Conjugate Silyl Transfer: 1,4-Addition of Silyl Boronic Esters to Cyclic Enones and Lactones,
Angew. Chem. 2006, 118, 5803-5805;
Angew. Chem. Int. Ed. 2006, 45, 5675-5677 [604]. (Abstract [605])
Selected a "Hot Paper" by Angewandte Chemie.
Highlighted in SYNFACTS 2006, 1142 [606].
Included into Organic Chemistry Highlights under www.organic-chemistry.org [607].

Lupe [608]

43.
S. Rendler, G. Auer, M. Keller, and M. Oestreich,
Preparation of a Privileged Silicon-Stereogenic Silane: Classical versus Kinetic Resolution,
Adv. Synth. Catal. 2006, 348, 1171-1182 [609]. (Abstract [610])

Lupe [611]

42.
M. Oestreich, F. Sempere-Culler, and A. B. Machotta,
An Enantioselective Access to the Anthracycline AB Synthon by a Desymmetrizing Heck Cyclization
(Special Issue dedicated to Professor Richard F. Heck),
Synlett 2006, 2965-2968 [612]. (Abstract [613])

Lupe [614]

41.
G. Auer, B. Weiner, and M. Oestreich,
Copper-Free and Copper-Promoted Conjugate Addition Reactions of Bis(triorganosilyl) Zincs and Tris(triorganosilyl) Zincates
(Special Issue dedicated to Professor Dieter Hoppe on the occasion of his 65th birthday),
Synthesis 2006, 2113-2116 [615]. (Abstract [616])

Lupe [617]

40.
M. Oestreich,
Trendbericht 2005 - Organische Chemie: Metallfreie Synthesemethoden,
Nachr. Chem. 2006, 54, 254-255 [618]. (Abstract [619])

Lupe [620]

39.
M. Oestreich,
Quaternary Stereocenters. Edited by Jens Christoffers and Angelika Baro. Wiley-VCH, Weinheim 2005 (Book Review),
Angew. Chem. 2006, 118, 554-555;
Angew. Chem. Int. Ed. 2006, 45, 540-541 [621]. (Abstract [622])

Lupe [623]

38.
G. Auer and M. Oestreich,
Silylzincation of Carbon-Carbon Multiple Bonds Revisited,
Chem. Commun. 2006, 311-313 [624]. (Abstract [625])

Lupe [626]

37.
M. Oestreich,
Chirality Transfer from Silicon to Carbon (Concept),
Chem. Eur. J. 2006, 12, 30-37 [627]. (Abstract [628])

2005

Lupe [629]

36.
S. Rendler, G. Auer, and M. Oestreich,
Kinetic Resolution of Chiral Secondary Alcohols by Dehydrogenative Coupling with Recyclable Silicon-Stereogenic Silanes,
Angew. Chem. 2005, 117, 7793-7797;
Angew. Chem. Int. Ed. 2005, 44, 7620-7624. [630] (Abstract [631])

Lupe [632]

35.
A. B. Machotta and M. Oestreich,
OMCOS 13 (Conference Report),
Nachr. Chem. 2005, 53, 1069 [633]. (Abstract [634])

Lupe [635]

34.
M. Oestreich,
Kaleidoscope of Catalysis: Heidelberg Forum of Molecular Catalysis 2005 (Conference Report),
Angew. Chem. 2005, 117, 5296-5297;
Angew. Chem. Int. Ed. 2005, 44, 5166-5167 [636]. (Abstract [637])

Lupe [638]

33.
S. Rendler and M. Oestreich,
Hypervalent Silicon as a Reactive Site in Selective Bond Forming Processes (Review),
Synthesis 2005, 1727-1747 [639]. (Abstract [640])

Lupe [641]

32.
M. Oestreich,
Swiss Delight: Bürgenstock 2005 (Conference Report),
Angew. Chem. 2005, 117, 3578-3580;
Angew. Chem. Int. Ed. 2005, 44, 3512-3513 [642]. (Abstract [643])

Lupe [644]

31.
M. Oestreich,
Chemie-Nachwuchsgruppenleiter in Freiburg (Conference Report),
Nachr. Chem. 2005, 53, 559 [645]. (Abstract [646])

Lupe [647]

30.
M. Oestreich,
Strategies for Catalytic Asymmetric Electrophilic α-Halogenation of Carbonyl Compounds (Highlight),
Angew. Chem. 2005, 117, 2376-2379;
Angew. Chem. Int. Ed. 2005, 44, 2324-2327 [648]. (Abstract [649])

Lupe [650]

29.
M. Oestreich and G. Auer,
Practical Synthesis of Allylic Silanes from Allylic Esters and Carbamates by Stereoselective Copper-Catalyzed Allylic Substitution Reactions,
Adv. Synth. Catal. 2005, 347, 637-640 [651]. (Abstract [652])

Lupe [653]

28.
M. Oestreich and S. Rendler,
"True" Chirality Transfer from Silicon to Carbon: Asymmetric Amplification in a Reagent-controlled Palladium-catalyzed Hydrosilylation,
Angew. Chem. 2005, 117, 1688-1691;
Angew. Chem. Int. Ed. 2005, 44, 1661-1664 [654]. (Abstract [655])
Highlighted in SYNFACTS 2005, 39 (Pilot Issue) [656].

Lupe [657]

27.
M. Oestreich,
Trendbericht 2004 - Organische Chemie: Metallfreie Synthesemethoden,
Nachr. Chem. 2005, 53, 267 [658]. (Abstract [659])

Lupe [660]

26.
M. Oestreich,
Neighbouring Group Effects in Heck Reactions (Review),
Eur. J. Org. Chem. 2005, 783-792 [661]. (Abstract [662])

Lupe [663]

25.
M. Oestreich, G. Auer, and M. Keller,
On the Mechanism of the Reductive Metalation of Asymmetrically Substituted Silyl Chlorides,
Eur. J. Org. Chem. 2005, 184-195 [664]. (Abstract [665])

Lupe [666]

24.
M. Oestreich, F. Sempere-Culler, and A. B. Machotta,
Catalytic Desymmetrizing Intramolecular Heck Reaction: Evidence for an Unusual Hydroxy-directed Migratory Insertion,
Angew. Chem. 2005, 117, 152-155;
Angew. Chem. Int. Ed. 2005, 44, 149-152 [667]. (Abstract [668])

2004

Lupe [669]

23.
M. Oestreich,
Synthese im Blickpunkt: Phosphine: Chemische Alleskönner?,
Nachr. Chem. 2004, 52, 1257-1260 [670]. (Abstract [671])

Lupe [672]

22.
M. Oestreich,
Synthese im Blickpunkt: Biomimetische Diterpen-Synthesen,
Nachr. Chem. 2004, 52, 1050-1055 [673]. (Abstract [674])

Lupe [675]

21.
M. Oestreich and B. Weiner,
Copper-catalyzed Conjugate Addition of a Bis(triorganosilyl) Zinc and a Methyl(triorganosilyl) Magnesium,
Synlett 2004, 2139-2142 [676]. (Abstract [677])

Lupe [678]

20.
M. Oestreich,
Synthese im Blickpunkt: Niedervalentes Titan: der Herr der kleinen Ringe,
Nachr. Chem. 2004, 52, 805-808 [679]. (Abstract [680])

Lupe [681]

19.
M. Oestreich,
Synthese im Blickpunkt: Wege zu (-)-Galanthamin,
Nachr. Chem. 2004, 52, 688-691 [682]. (Abstract [683])

Lupe [684]

18.
M. Oestreich,
Synthese im Blickpunkt: Ein neues Eisen im Feuer,
Nachr. Chem. 2004, 52, 446-449 [685]. (Abstract [686])

Lupe [687]

17.
M. Oestreich and F. Sempere-Culler,
Facile Protocol for the Highly Regioselective and Stereodivergent Synthesis of Substituted Bishomoallylic Alcohols from Esters,
Chem. Commun. 2004, 692-693 [688]. (Abstract [689])

Lupe [690]

16.
M. Oestreich,
Trendbericht 2003 - Organische Chemie: Metallfreie Synthesemethoden,
Nachr. Chem. 2004, 52, 282-283 [691]. (Abstract [692])

Lupe [693]

15.
M. Oestreich,
Der Triumphzug der Metathese in drei Bänden: Handbook of Metathesis. Vol. 1-3. Hrsg. von Robert H. Grubbs. Wiley-VCH, Weinheim 2003 (Book Review),
Nachr. Chem. 2004, 52, 184-185 [694]. (Abstract [695])

Lupe [696]

14.
M. Oestreich,
23. Regio-Symposium in Falkau/Schwarzwald (Conference Report),
Nachr. Chem. 2004, 52, 64 [697]. (Abstract [698])

Lupe [699]

13.
M. Oestreich,
Synthese im Blickpunkt: Das andere Gesicht der Organokatalyse,
Nachr. Chem. 2004, 52, 35-38 [700]. (Abstract [701])

2003

Lupe [702]

12.
M. Oestreich, U. K. Schmid, G. Auer, and M. Keller,
A Convergent Method for the Synthesis of Highly Enantiomerically Enriched Cyclic Silanes with Silicon-Centered Chirality (Feature Article),
Synthesis 2003, 2725-2739 [703]. (Abstract [704])

Lupe [705]

11.
M. Oestreich,
Trendbericht 2002 - Organische Chemie: Metallfreie Synthesemethoden,
Nachr. Chem. 2003, 51, 298-300 [706]. (Abstract [707])

1999

Lupe [708]

10.
M. Oestreich and E. Droste,
Hochreaktive Mehrfachbindungssysteme: Theorie und Experiment (Conference Report),
Nachr. Chem. Tech. Lab. 1999, 47, 219 [709]. (Abstract [710])

Publications with Professor Larry E. Overman

9.
A. B. Dounay, K. Hatanaka, J. J. Kodanko, M. Oestreich, L. E. Overman, L. A. Pfeifer, and M. M. Weiss,
Catalytic Asymmetric Synthesis of Quaternary Carbons Bearing Two Aryl Substituents. Enantioselective Synthesis of 3-Alkyl-3-Aryl Oxindoles by Catalytic Asymmetric Intramolecular Heck Reactions,
J. Am. Chem. Soc. 2003, 125, 6261-6271 [711]. (Abstract [712])

8.
M. Oestreich, P. R. Dennison, J. J. Kodanko, and L. E. Overman,
Thwarting β-Hydride Elimination: Capture of the Alkylpalladium Intermediate of an Asymmetric Intramolecular Heck Reaction,
Angew. Chem. 2001, 113, 1485-1489;
Angew. Chem. Int. Ed. 2001, 40, 1439-1442 [713]. (Abstract [714])

Publications with Professor Dieter Hoppe

7.
M. Oestreich and D. Hoppe,
Stereospecific Preparation of Highly Enantiomerically Enriched Organomagnesium Reagents (Review and Commentary),
Chemtracts - Organic Chemistry 2001, 14, 100-105.

6.
M. Oestreich, R. Fröhlich, and D. Hoppe,
(-)-Sparteine-mediated Stereoselective Intramolecular Carbolithiation of 4-Substituted 5-Hexynyl Carbamates. Synthesis of Enantiopure 1,3-Difunctionalized Alkylidene Cyclopentanes,
J. Org. Chem. 1999, 64, 8616-8626 [715]. (Abstract [716])

5.
D. Hoppe, M. J. Woltering, M. Oestreich, and R. Fröhlich,
(-)-Sparteine-Mediated Stereoselective Intramolecular Carbolithiation of Alkenes: Synthesis of Enantiopure Cyclopentanes with Three Consecutive Stereogenic Centers,
Helv. Chim. Acta 1999, 82, 1860-1877 [717]. (Abstract [718])

4.
M. Oestreich and D. Hoppe,
(-)-Sparteine-mediated Stereoselective Intramolecular Conjugate Addition Reactions of Dienes and Enynes,
Tetrahedron Lett. 1999, 40, 1881-1884 [719]. (Abstract)
[720]Corrigendum, Tetrahedron Lett. 1999, 40, 3283 [721]. (Abstract [722])

3.
M. Oestreich, R. Fröhlich, and D. Hoppe,
(-)-Sparteine-mediated Stereoselective Intramolecular Carbolithiation of Alkynes,
Tetrahedron Lett. 1998, 39, 1745-1748 [723]. (Abstract [724])

Publications with Professor Paul Knochel

2.
A. Boudier, C. Darcel, F. Flachsmann, L. Micouin, M. Oestreich, and P. Knochel,
Stereoselective Preparation and Reactions of Configurationally Defined Dialkylzinc Compounds,
Chem. Eur. J. 2000, 6, 2748-2761 [725]. (Abstract [726])

1.
L. Micouin, M. Oestreich, and P. Knochel,
Stereoselective Preparation and Reactions of Cycloalkylzinc Compounds,
Angew. Chem. 1997, 109, 275-276;
Angew. Chem. Int. Ed. 1997, 36, 245-246 [727]. (Abstract [728])

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