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Inhalt des Dokuments

2018

251.
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 Silylium Ion/Phosphane Frustrated and Conventional Lewis Pairs,
submitted for publication.

250.
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,
submitted for publication.

249.
W. Chen and M. Oestreich,
Metal-Free Transfer Hydroiodination of C‒C Multiple Bonds,
in revision.

248.
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, accepted for publication.

247.
F. Forster and M. Oestreich,
Bioinspired Catalytic Generation of Main-Group Electrophiles by Cooperative Bond Activation (Account),
Chimia 2018, 72, accepted for publication.

Lupe

246.
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, asap on August 10, 2018. (Abstract)

245.
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. Int. Ed. 2018, 57, Accepted Article on August 2, 2018. (Abstract)
Highlighted as a "Very Important Paper (VIP)" by Angewandte Chemie.

Lupe

244.
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. Int. Ed. 2018, 57, early view on July 26, 2018. (Abstract)

Lupe

243.
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 2018, 37, asap on July 23, 2018. (Abstract)

Lupe

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. 2018, 57, 10728-10731. (Abstract)
Selected as a "Hot Paper" by Angewandte Chemie.
Featured on the Inside Back Cover of Angewandte Chemie.

Lupe

241.
J.-J. Feng and M. Oestreich,
Copper-Catalyzed Silylation of C(sp3)-H Bonds Adjacent to Amide Nitrogen Atoms,
Org. Lett. 2018, 20, 4273-4276. (Abstract)

Lupe

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, 9317-9320;
Angew. Chem. Int. Ed. 2018, 57, 9176-9179. (Abstract)

Lupe

239.
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,
Chem. Sci. 2018, 9, 5600-5607. (Abstract)
Selected for the 2018 Chemical Science HOT Article Collection
(open access)

Lupe

238.
L. Omann, Z.-W. Qu, E. Irran, H. F. T. Klare, S. Grimme, and M. Oestreich,
Electrophilic Formylation of Arenes by Silylium Ion Mediated Activation of Carbon Monoxide,
Angew. Chem. 2018, 130, 8433-8437;
Angew. Chem. Int. Ed. 2018, 57, 8301-8305. (Abstract)

Lupe

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. (Abstract)
Part of A Dutch-German Initiative Virtual Issue.
Part of Board Member Virtual Issue.
(open access)

Lupe

236.
W. Yuan, P. Smirnov, and M. Oestreich,
Custom Hydrosilane Synthesis Based on Monosilane,
Chem 2018, 4, 1443-1450. (Abstract)
FREE ACCESS AVAILABLE!

Lupe

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. 2018, 2290-2293. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)

2017

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2018, 14, 165.

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Featured on the Front Cover of JACS.

Lupe

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. (Abstract)
Featured on the Front Cover of Dalton Transactions.

Lupe

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. (Abstract)

Lupe

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),
Synlett 2017, 28, 2411-2414. (Abstract)

Preface by M. Oestreich,
Synlett 2017, 28, 2394-2395. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)
(open access)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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]
Chem. Eur. J. 2017, 23, 6213-6219. (Abstract)

Lupe

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]
Chem. Eur. J. 2017, 23, 5925-5928. (Abstract)

Lupe

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 (Ed.: M. Oestreich), Thieme, Stuttgart, 2017, 65-176. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2017, 13, 529.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Featured on the Cover of Organometallics.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

2016

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)
ACS AuthorChoice (open access)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
ACS AuthorChoice (open access)
Highlighted in SYNFACTS 2016, 12, 971.

Lupe

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2016, 12, 729.

Lupe

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. (Abstract)

Lupe

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. (Abstract)
ACS AuthorChoice (open access)

Lupe

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. (Abstract)

Lupe

188.
A. Hensel and M. Oestreich,
Asymmetric Addition of Boron and Silicon Nucleophiles,
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

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

2015

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
(open access)

Lupe

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

Lupe

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. (Abstract)

Lupe

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

Lupe

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)
ACS AuthorChoice (open access)

Lupe

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. (Abstract)
(open access)

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2015, 11, 829.

Lupe

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. (Abstract)
ACS AuthorChoice (open access)
Highlighted to SYNFACTS 2015, 11, 855.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

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

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. (Abstract)
ACS AuthorChoice (open access)

Lupe

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. (Abstract)
(open access)

Lupe

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. (Abstract)
Featured on the Cover of Organometallics.

Lupe

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. (Abstract)

2014

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2015, 11, 79.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Highlighted in ChemCatChem 2014, 6, 2486-2489.

Lupe

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),
Chem. Eur. J. 2014, 20, 9250-9254. (Abstract)

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

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2014, 10, 840.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)

2013

Lupe

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

Lupe

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. (Abstract)

Lupe

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 (September/October issue).

Lupe

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

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2014, 10, 73.

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2013, 9, 1216.

Lupe

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. (Abstract)
Selected as a "Hot Paper" by Angewandte Chemie.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Featured on the Cover of ACS Catalysis.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2013, 9, 744.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

2012

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2012, 8, 1239.

Lupe

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

Lupe

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

Lupe

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

Lupe

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. (Abstract)
Included into Organic Chemistry Highlights under www.organic-chemistry.org.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

2011

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Included into Organic Chemistry Highlights under www.organic-chemistry.org.

Lupe

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

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. (Abstract)
Highlighted in Nachr. Chem. 2012, 60, 216-250.
Highlighted in Angew. Chem. Int. Ed. 2012, 51, 4526-4528.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)
Selected as EurBest in EurJOC.

Lupe

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

2010

Lupe

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. (Abstract)
Editors' Choice: ChemInform.

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2010, 549.

Lupe

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Selected a "Hot Article" by Chemical Communications.

Lupe

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

Lupe

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. (Abstract)

2009

Lupe

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. (Abstract)
Highlighted in Nachr. Chem. 2010, 58, 7.
Highlighted in Angew. Chem. Int. Ed. 2012, 51, 4526-4528.

Lupe

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. (Abstract)
Editors' Choice: Spotlights.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2009, 1002.

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)
Included into Organic Chemistry Highlights under www.organic-chemistry.org.

Lupe

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

Lupe

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

Lupe

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. (Abstract)

Lupe

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

2008

Lupe

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. (Abstract)

Lupe

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

Lupe

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2008, 855.

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2008, 739.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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

Lupe

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

Lupe

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. (Abstract)

2007

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (open access) (Abstract)

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2007, 409.

Lupe

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. (Abstract)

2006

Lupe

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

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

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Selected a "Hot Paper" by Angewandte Chemie.
Highlighted in SYNFACTS 2006, 1142.
Included into Organic Chemistry Highlights under www.organic-chemistry.org.

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)

Lupe

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

Lupe

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

2005

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)

Lupe

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

Lupe

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

Lupe

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)

Lupe

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. (Abstract)
Highlighted in SYNFACTS 2005, 39 (Pilot Issue).

Lupe

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

Lupe

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

Lupe

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. (Abstract)

Lupe

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. (Abstract)

2004

Lupe

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

Lupe

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

Lupe

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

Lupe

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

Lupe

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

Lupe

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

Lupe

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. (Abstract)

Lupe

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

Lupe

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. (Abstract)

Lupe

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

Lupe

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

2003

Lupe

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. (Abstract)

Lupe

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

1999

Lupe

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

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. (Abstract)

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. (Abstract)

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. (Abstract)

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. (Abstract)

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

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

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. (Abstract)

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. (Abstract)

Zusatzinformationen / Extras