Martin Oestreich - Publications

Affiliations: 
2011- Institut für Chemie Technische Universität Berlin, Berlin, Berlin, Germany 
Area:
Catalysis, Main-Group Chemistry, Reaction Mechanism
Website:
http://www.organometallics.tu-berlin.de

200 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Wu Q, Irran E, Müller R, Kaupp M, Klare HFT, Oestreich M. Characterization of hydrogen-substituted silylium ions in the condensed phase. Science (New York, N.Y.). 365: 168-172. PMID 31296768 DOI: 10.1126/science.aax9184  1
2019 Chen W, Oestreich M. Metal-Free Transfer Hydrobromination of C-C Triple Bonds. Organic Letters. PMID 31150253 DOI: 10.1021/acs.orglett.9b01431  1
2019 Mao W, Xue W, Irran E, Oestreich M. Copper-Catalyzed Regio- and Enantioselective Addition of Silicon Grignard Reagents to Alkenes Activated by Azaaryl Groups. Angewandte Chemie (International Ed. in English). PMID 31141281 DOI: 10.1002/anie.201905934  1
2019 Richter SC, Oestreich M. Bioinspired Metal-Free Formal Decarbonylation of α-Branched Aliphatic Aldehydes at Ambient Temperature. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31066944 DOI: 10.1002/chem.201902082  0.96
2019 Feng JJ, Oestreich M. Tertiary α-Silyl Alcohols by Diastereoselective Coupling of 1,3-Dienes and Acylsilanes Initiated by Enantioselective Copper-Catalyzed Borylation. Angewandte Chemie (International Ed. in English). PMID 30947388 DOI: 10.1002/anie.201903174  1
2019 Seliger J, Oestreich M. Making the Silylation of Alcohols Chiral: Asymmetric Protection of Hydroxy Groups. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30919539 DOI: 10.1002/chem.201900792  1
2019 Yi H, Oestreich M. Regiodivergent and Stereospecific Aziridine Opening by Copper-Catalyzed Addition of Silicon Grignard Reagents. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30888724 DOI: 10.1002/chem.201901128  1
2019 Xue W, Mao W, Zhang L, Oestreich M. Mechanistic Dichotomy of Magnesium- and Zinc-Based Germanium Nucleophiles in the C(sp3)-Ge Cross-Coupling with Alkyl Electrophiles. Angewandte Chemie (International Ed. in English). PMID 30839143 DOI: 10.1002/anie.201901860  1
2019 Yi H, Mao W, Oestreich M. Enantioselective Construction of alpha-Chiral Silanes by Nickel-Catalyzed C(sp3)-C(sp3) Cross-Coupling. Angewandte Chemie (International Ed. in English). PMID 30644631 DOI: 10.1002/anie.201814340  1
2019 Orecchia P, Yuan W, Oestreich M. Transfer Hydrocyanation of α- and α,β-Substituted Styrenes Catalyzed by Boron Lewis Acids. Angewandte Chemie (International Ed. in English). PMID 30624005 DOI: 10.1002/anie.201813853  1
2018 Seliger J, Dong X, Oestreich M. Kinetic Resolution of Tertiary Propargylic Alcohols by Enantioselective Cu-H-Catalyzed Si-O-Coupling. Angewandte Chemie (International Ed. in English). PMID 30570206 DOI: 10.1002/anie.201813229  1
2018 Chen W, Walker J, Oestreich M. Metal-Free Transfer Hydroiodination of C-C Multiple Bonds. Journal of the American Chemical Society. PMID 30550280 DOI: 10.1021/jacs.8b12318  1
2018 Zhang L, Oestreich M. Copper-Catalyzed Cross-Coupling of Vinyliodonium Salts and Zinc-Based Silicon Nucleophiles. Organic Letters. PMID 30539631 DOI: 10.1021/acs.orglett.8b03714  1
2018 Yuan W, Orecchia P, Oestreich M. Palladium-Catalyzed Three-Component Reaction of Dihydrosilanes and Vinyl Iodides in the Presence of Alcohols: Rapid Assembly of Silyl Ethers of Tertiary Silanes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30431674 DOI: 10.1002/chem.201805595  1
2018 Shaykhutdinova P, Oestreich M. Achieving Enantioselectivity in Difficult Cyclohexa-1,3-diene Diels-Alder Reactions with Sulfur-Stabilized Silicon Cations as Lewis Acid Catalysts. Organic Letters. PMID 30362776 DOI: 10.1021/acs.orglett.8b02945  1
2018 Walker JCL, Oestreich M. Regioselective Transfer Hydrodeuteration of Alkenes with a Hydrogen Deuteride Surrogate Using B(CF) Catalysis. Organic Letters. 20: 6411-6414. PMID 30336676 DOI: 10.1021/acs.orglett.8b02718  1
2018 Forster F, Oestreich M. Bioinspired Catalytic Generation of Main-group Electrophiles by Cooperative Bond Activation. Chimia. 72: 584-588. PMID 30257731 DOI: 10.2533/chimia.2018.584  0.8
2018 Müller T, Merk A, Großekappenberg H, Luecke MP, Lorent C, Driess M, Oestreich M, Klare H. Single-Electron Transfer Reactions in Silylium Ion/Phosphane Frustrated and Conventional Lewis Pairs. Angewandte Chemie (International Ed. in English). PMID 30178534 DOI: 10.1002/anie.201808922  1
2018 Hazrati H, Oestreich M. Copper-Catalyzed Double C(sp)-Si Coupling of Geminal Dibromides: Ionic-to-Radical Switch in the Reaction Mechanism. Organic Letters. PMID 30095263 DOI: 10.1021/acs.orglett.8b02281  1
2018 Omann L, Pudasaini B, Irran E, Klare HFT, Baik MH, Oestreich M. Thermodynamic kinetic control in substituent redistribution reactions of silylium ions steered by the counteranion. Chemical Science. 9: 5600-5607. PMID 30061992 DOI: 10.1039/c8sc01833b  1
2018 Süsse L, Vogler M, Mewald M, Kemper B, Irran E, Oestreich M. Enantioselective Nazarov Cyclizations Catalyzed by an Axial Chiral, C6F5-Substituted Boron Lewis Acid. Angewandte Chemie (International Ed. in English). PMID 29978948 DOI: 10.1002/anie.201806011  1
2018 Feng JJ, Oestreich M. Copper-Catalyzed Silylation of C(sp)-H Bonds Adjacent to Amide Nitrogen Atoms. Organic Letters. PMID 29956941 DOI: 10.1021/acs.orglett.8b01698  1
2018 Wu Q, Qu ZW, Omann L, Irran E, Klare H, Oestreich M. Cleavage of Unactivated Si-C(sp3) Bonds with Reed's Carborane Acids: Clean Formation of Known and Unknown Silylium Ions. Angewandte Chemie (International Ed. in English). PMID 29775241 DOI: 10.1002/anie.201805637  1
2018 Omann L, Qu ZW, Irran E, Klare H, Grimme S, Oestreich M. Electrophilic Formylation of Arenes by Silylium Ion-Mediated Activation of Carbon Monoxide. Angewandte Chemie (International Ed. in English). PMID 29741219 DOI: 10.1002/anie.201803181  1
2018 Dong X, Kita Y, Oestreich M. Kinetic Resolution of alpha-Hydroxy-Substituted Oxime Ethers by Enantioselective Cu-H-Catalyzed Si-O Coupling. Angewandte Chemie (International Ed. in English). PMID 29645338 DOI: 10.1002/anie.201802947  1
2018 Forster F, Rendón López VM, Oestreich M. Catalytic Dehydrogenative Stannylation of C(sp)-H Bonds Involving Cooperative Sn-H Bond Activation of Hydrostannanes. Journal of the American Chemical Society. PMID 29338212 DOI: 10.1021/jacs.7b13088  0.8
2017 Scharfbier J, Hazrati H, Irran E, Oestreich M. Copper-Catalyzed Substitution of α-Triflyloxy Nitriles and Esters with Silicon Nucleophiles under Inversion of the Configuration. Organic Letters. 19: 6562-6565. PMID 29192788 DOI: 10.1021/acs.orglett.7b03279  1
2017 Forster F, Metsanen TT, Irran E, Hrobarik P, Oestreich M. Cooperative Al-H Bond Activation in DIBAL-H: Catalytic Generation of an Alumenium-Ion-Like Lewis Acid for Hydrodefluorinative Friedel-Crafts Alkylation. Journal of the American Chemical Society. PMID 28985070 DOI: 10.1021/jacs.7b09444  0.92
2017 Luecke MP, Porwal D, Kostenko A, Zhou YP, Yao S, Keck M, Limberg C, Oestreich M, Driess M. Bis(silylenyl)-substituted ferrocene-stabilized η(6)-arene iron(0) complexes: synthesis, structure and catalytic application. Dalton Transactions (Cambridge, England : 2003). PMID 28967014 DOI: 10.1039/c7dt03301j  1
2017 Keess S, Oestreich M. Cyclohexa-1,4-dienes in transition-metal-free ionic transfer processes. Chemical Science. 8: 4688-4695. PMID 28936336 DOI: 10.1039/c7sc01657c  1
2017 Yuan W, Orecchia P, Oestreich M. Cyclohexa-1,3-diene-based dihydrogen and hydrosilane surrogates in B(C6F5)3-catalysed transfer processes. Chemical Communications (Cambridge, England). PMID 28876009 DOI: 10.1039/c7cc06195a  1
2017 Xue W, Oestreich M. Copper-Catalyzed Decarboxylative Radical Silylation of Redox-Active Aliphatic Carboxylic Acid Derivatives. Angewandte Chemie (International Ed. in English). PMID 28742250 DOI: 10.1002/anie.201706611  1
2017 Dong X, Weickgenannt A, Oestreich M. Broad-spectrum kinetic resolution of alcohols enabled by Cu-H-catalysed dehydrogenative coupling with hydrosilanes. Nature Communications. 8: 15547. PMID 28569754 DOI: 10.1038/ncomms15547  1
2017 Yin Q, Oestreich M. Photocatalysis Enabling Acceptorless Dehydrogenation of Benzofused Saturated Rings at Room Temperature. Angewandte Chemie (International Ed. in English). PMID 28464504 DOI: 10.1002/anie.201703536  1
2017 Omann L, Königs CD, Klare HF, Oestreich M. Cooperative Catalysis at Metal-Sulfur Bonds. Accounts of Chemical Research. PMID 28406290 DOI: 10.1021/acs.accounts.7b00089  1
2017 Liu WB, Schuman DP, Yang YF, Toutov AA, Liang Y, Klare HF, Nesnas N, Oestreich M, Blackmond DG, Virgil SC, Banerjee S, Zare RN, Grubbs RH, Houk KN, Stoltz BM. KOt-Bu-Catalyzed Dehydrogenative C-H Silylation of Heteroaromatics: A Combined Experimental and Computational Mechanistic Study. Journal of the American Chemical Society. PMID 28403611 DOI: 10.1021/jacs.6b13031  1
2017 Keess S, Oestreich M. Access to Fully Alkylated Germanes by B(C6F5)3-Catalyzed Transfer Hydrogermylation of Alkenes. Organic Letters. PMID 28358201 DOI: 10.1021/acs.orglett.7b00672  1
2017 Yin Q, Klare HF, Oestreich M. Catalytic Friedel-Crafts C-H Borylation of Electron-Rich Arenes: Dramatic Rate Acceleration by Added Alkenes. Angewandte Chemie (International Ed. in English). PMID 28244623 DOI: 10.1002/anie.201611536  1
2017 Wübbolt S, Maji MS, Irran E, Oestreich M. A Tethered Ru-S Complex with an Axial Chiral Thiolate Ligand for Cooperative Si-H Bond Activation: Application to Enantioselective Imine Reduction. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28191742 DOI: 10.1002/chem.201700304  1
2017 Chatterjee I, Porwal D, Oestreich M. B(C6 F5 )3 -Catalyzed Chemoselective Defunctionalization of Ether-Containing Primary Alkyl Tosylates with Hydrosilanes. Angewandte Chemie (International Ed. in English). PMID 28181397 DOI: 10.1002/anie.201611813  1
2016 Klare HF, Oestreich M. Teaching nature the unnatural. Science (New York, N.Y.). 354: 970. PMID 27884992 DOI: 10.1126/science.aal1951  1
2016 Keess S, Oestreich M. 3-tert-Butyl-Substituted Cyclohexa-1,4-dienes as Isobutane Equivalents in the B(C6 F5 )3 -Catalyzed Transfer Hydro-tert-Butylation of Alkenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27775187 DOI: 10.1002/chem.201604397  1
2016 Xue W, Qu ZW, Grimme S, Oestreich M. Copper-Catalyzed Cross-Coupling of Silicon Pronucleophiles with Unactivated Alkyl Electrophiles Coupled with Radical Cyclization. Journal of the American Chemical Society. PMID 27744687 DOI: 10.1021/jacs.6b09596  1
2016 Mohr J, Oestreich M. Balancing C=C Functionalization and C=O Reduction in Cu-H Catalysis. Angewandte Chemie (International Ed. in English). PMID 27490748 DOI: 10.1002/anie.201606701  1
2016 Yin Q, Kemper S, Klare H, Oestreich M. Boron Lewis Acid-Catalyzed Hydroboration of Alkenes with Pinacolborane: BArF3 Does What B(C6F5)3 Cannot Do! Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27447683 DOI: 10.1002/chem.201603466  1
2016 Lefranc A, Qu ZW, Grimme S, Oestreich M. Hydrogenation and Transfer Hydrogenation Promoted by Tethered Ru-S Complexes: From Cooperative Dihydrogen Activation to Hydride Abstraction/Proton Release from Dihydrogen Surrogates. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 27311877 DOI: 10.1002/chem.201600386  1
2016 Chen QA, Klare HF, Oestreich M. Brønsted Acid-Promoted Formation of Stabilized Silylium Ions for Catalytic Friedel-Crafts C-H Silylation. Journal of the American Chemical Society. PMID 27303857 DOI: 10.1021/jacs.6b04878  1
2016 Süsse L, Hermeke J, Oestreich M. The Asymmetric Piers Hydrosilylation. Journal of the American Chemical Society. PMID 27212565 DOI: 10.1021/jacs.6b03443  1
2016 Chatterjee I, Oestreich M. Brønsted Acid-Catalyzed Transfer Hydrogenation of Imines and Alkenes Using Cyclohexa-1,4-dienes as Dihydrogen Surrogates. Organic Letters. PMID 27181437 DOI: 10.1021/acs.orglett.6b01016  1
2016 Fopp C, Romain E, Isaac K, Chemla F, Ferreira F, Jackowski O, Oestreich M, Perez-Luna A. Stereodivergent Silylzincation of α-Heteroatom-Substituted Alkynes. Organic Letters. PMID 27091113 DOI: 10.1021/acs.orglett.6b00680  1
2016 Schmidt RK, Klare HF, Fröhlich R, Oestreich M. Planar Chiral, Ferrocene-Stabilized Silicon Cations. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26929105 DOI: 10.1002/chem.201504777  1
2016 Yin Q, Klare HF, Oestreich M. Friedel-Crafts-Type Intermolecular C-H Silylation of Electron-Rich Arenes Initiated by Base-Metal Salts. Angewandte Chemie (International Ed. in English). PMID 26821860 DOI: 10.1002/anie.201510469  1
2015 Metsänen TT, Gallego D, Szilvási T, Driess M, Oestreich M. Peripheral mechanism of a carbonyl hydrosilylation catalysed by an SiNSi iron pincer complex. Chemical Science. 6: 7143-7149. PMID 29861950 DOI: 10.1039/c5sc02855h  1
2015 Stahl T, Hrobárik P, Königs CDF, Ohki Y, Tatsumi K, Kemper S, Kaupp M, Klare HFT, Oestreich M. Mechanism of the cooperative Si-H bond activation at Ru-S bonds. Chemical Science. 6: 4324-4334. PMID 29218203 DOI: 10.1039/c5sc01035g  1
2015 Oestreich M. Transfer Hydrosilylation. Angewandte Chemie (International Ed. in English). PMID 26597123 DOI: 10.1002/anie.201508879  1
2015 Wübbolt S, Oestreich M. Catalytic Electrophilic CH Silylation of Pyridines Enabled by Temporary Dearomatization. Angewandte Chemie (International Ed. in English). PMID 26593854 DOI: 10.1002/anie.201508181  1
2015 Mohr J, Porwal D, Chatterjee I, Oestreich M. Extending the Scope of the B(C6 F5 )3 -Catalyzed CN Bond Reduction: Hydrogenation of Oxime Ethers and Hydrazones. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26489785 DOI: 10.1002/chem.201503509  1
2015 Chatterjee I, Qu ZW, Grimme S, Oestreich M. B(C6 F5 )3 -Catalyzed Transfer of Dihydrogen from One Unsaturated Hydrocarbon to Another. Angewandte Chemie (International Ed. in English). 54: 12158-62. PMID 26418183 DOI: 10.1002/anie.201504941  1
2015 Simonneau A, Oestreich M. Formal SiH4 chemistry using stable and easy-to-handle surrogates. Nature Chemistry. 7: 816-22. PMID 26391081 DOI: 10.1038/nchem.2329  1
2015 Jiao LY, Ferreira AV, Oestreich M. Phosphinic Amide as Directing Group Enabling Palladium(II)-Catalyzed ortho C-H Alkenylation of Anilines without and with Alkylation at the Nitrogen Atom. Chemistry, An Asian Journal. PMID 26370493 DOI: 10.1002/asia.201500829  1
2015 Omann L, Oestreich M. A Catalytic SE Ar Approach to Dibenzosiloles Functionalized at Both Benzene Cores. Angewandte Chemie (International Ed. in English). 54: 10276-9. PMID 26177933 DOI: 10.1002/anie.201504066  1
2015 Hensel A, Oestreich M. Asymmetric catalysis with silicon-based cuprates: enantio- and regioselective allylic substitution of linear precursors. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 9062-5. PMID 25965581 DOI: 10.1002/chem.201501371  1
2015 Pareek M, Fallon T, Oestreich M. Platinum(0)-Catalyzed Indolyne Insertion into Bis(pinacolato)diboron Followed by Site-Selective Suzuki-Miyaura Cross-Coupling. Organic Letters. 17: 2082-5. PMID 25880022 DOI: 10.1021/acs.orglett.5b00604  1
2015 Fallon T, Oestreich M. A Constellation of Deuterium-Labeled Silanes as a Simple Mechanistic Probe not Requiring Absolute Configuration Determination. Angewandte Chemie (International Ed. in English). 54: 12488-91. PMID 25800438 DOI: 10.1002/anie.201500750  1
2015 Simonneau A, Oestreich M. Fascinating hydrogen atom transfer chemistry of alkenes inspired by problems in total synthesis. Angewandte Chemie (International Ed. in English). 54: 3556-8. PMID 25703197 DOI: 10.1002/anie.201500557  1
2015 Oestreich M, Hermeke J, Mohr J. A unified survey of Si-H and H-H bond activation catalysed by electron-deficient boranes. Chemical Society Reviews. 44: 2202-20. PMID 25679769 DOI: 10.1039/c4cs00451e  1
2015 Chatterjee I, Oestreich M. B(C6F5)3-catalyzed transfer hydrogenation of imines and related heteroarenes using cyclohexa-1,4-dienes as a dihydrogen source. Angewandte Chemie (International Ed. in English). 54: 1965-8. PMID 25529119 DOI: 10.1002/anie.201409246  1
2015 Delvos LB, Oestreich M. Temperature-Dependent Direct Enantioconvergent Silylation of a Racemic Cyclic Allylic Phosphate by Copper(I)-Catalyzed Allylic Substitution Synthesis (Germany). 47: 924-933. DOI: 10.1055/s-0034-1380157  1
2015 Metsänen TT, Gallego D, Szilvási T, Driess M, Oestreich M. Peripheral mechanism of a carbonyl hydrosilylation catalysed by an SiNSi iron pincer complex Chemical Science. 6: 7143-7149. DOI: 10.1039/c5sc02855h  1
2015 Stahl T, Hrobárik P, Königs CDF, Ohki Y, Tatsumi K, Kemper S, Kaupp M, Klare HFT, Oestreich M. Mechanism of the cooperative Si-H bond activation at Ru-S bonds Chemical Science. 6: 4324-4334. DOI: 10.1039/c5sc01035g  1
2015 Keess S, Simonneau A, Oestreich M. Direct and transfer hydrosilylation reactions catalyzed by fully or partially fluorinated triarylboranes: A systematic study Organometallics. 34: 790-799. DOI: 10.1021/om501284a  1
2015 Metsänen TT, Oestreich M. Temperature-dependent chemoselective hydrosilylation of carbon dioxide to formaldehyde or methanol oxidation state Organometallics. 34: 543-546. DOI: 10.1021/om501279a  1
2015 Simonneau A, Biberger T, Oestreich M. The Cyclohexadienyl-Leaving-Group Approach toward Donor-Stabilized Silylium Ions Organometallics. 34: 3927-3929. DOI: 10.1021/acs.organomet.5b00609  1
2015 Rohde VHG, Müller MF, Oestreich M. Intramolecularly Sulfur-Stabilized Silicon Cations with Chiral Binaphthyl Backbones: Synthesis of Three Different Motifs and Their Application in Enantioselective Diels-Alder Reactions Organometallics. 34: 3358-3373. DOI: 10.1021/acs.organomet.5b00351  1
2015 Zhou X, Szeker K, Jiao LY, Oestreich M, Mikhailopulo IA, Neubauer P. Synthesis of 2,6-dihalogenated purine nucleosides by thermostable nucleoside phosphorylases Advanced Synthesis and Catalysis. 357: 1237-1244. DOI: 10.1002/adsc.201400966  1
2014 Jiao LY, Smirnov P, Oestreich M. Exceptionally mild palladium(II)-catalyzed dehydrogenative C-H/C-H arylation of indolines at the C-7 position under air. Organic Letters. 16: 6020-3. PMID 25375317 DOI: 10.1021/ol503035z  1
2014 Mohr J, Oestreich M. B(C6F5)3-catalyzed hydrogenation of oxime ethers without cleavage of the N-O bond. Angewandte Chemie (International Ed. in English). 53: 13278-81. PMID 25283891 DOI: 10.1002/anie.201407324  1
2014 Romain E, Fopp C, Chemla F, Ferreira F, Jackowski O, Oestreich M, Perez-Luna A. Trans-selective radical silylzincation of ynamides. Angewandte Chemie (International Ed. in English). 53: 11333-7. PMID 25160825 DOI: 10.1002/anie.201407002  1
2014 Hazra CK, Fopp C, Oestreich M. Copper(I)-catalyzed regioselective addition of nucleophilic silicon across terminal and internal carbon-carbon triple bonds. Chemistry, An Asian Journal. 9: 3005-10. PMID 25065952 DOI: 10.1002/asia.201402643  1
2014 Driess M, Oestreich M. New frontiers and challenges in silicon chemistry: ISOS XVII in Berlin. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 9144-5. PMID 25042099 DOI: 10.1002/chem.201404080  1
2014 Hermeke J, Klare HF, Oestreich M. Direct catalytic access to N-silylated enamines from enolizable imines and hydrosilanes by base-free dehydrogenative Si-N coupling. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 9250-4. PMID 24867619 DOI: 10.1002/chem.201402866  1
2014 Metsänen TT, Hrobárik P, Klare HF, Kaupp M, Oestreich M. Insight into the mechanism of carbonyl hydrosilylation catalyzed by Brookhart's cationic iridium(III) pincer complex. Journal of the American Chemical Society. 136: 6912-5. PMID 24784900 DOI: 10.1021/ja503254f  1
2014 Hensel A, Nagura K, Delvos LB, Oestreich M. Enantioselective addition of silicon nucleophiles to aldimines using a preformed NHC-Copper(I) complex as the catalyst. Angewandte Chemie (International Ed. in English). 53: 4964-7. PMID 24700790 DOI: 10.1002/anie.201402086  1
2014 Oestreich M. Breaking news on the enantioselective intermolecular Heck reaction. Angewandte Chemie (International Ed. in English). 53: 2282-5. PMID 24481834 DOI: 10.1002/anie.201310585  1
2014 Delvos LB, Hensel A, Oestreich M. McQuade's six-membered NHC-copper(I) Complexes for catalytic asymmetric silyl transfer Synthesis (Germany). 46: 2957-2964. DOI: 10.1055/s-0034-1378542  1
2014 Hermeke J, Mewald M, Irran E, Oestreich M. Chemoselective tin-boron exchange aided by the use of dummy ligands at the tin atom Organometallics. 33: 5097-5100. DOI: 10.1021/om500851r  1
2014 Rohde VHG, Pommerening P, Klare HFT, Oestreich M. Intramolecularly sulfur-stabilized silicon cations as Lewis acid catalysts Organometallics. 33: 3618-3628. DOI: 10.1021/om500570d  1
2014 Redies KM, Fallon T, Oestreich M. En route to stable all-carbon-substituted silylenes: Synthesis and reactivity of a bis(α-spirocyclopropyl)silylene Organometallics. 33: 3235-3238. DOI: 10.1021/om500485m  1
2014 Mohr J, Durmaz M, Irran E, Oestreich M. Tris(5,6,7,8-tetrafluoronaphthalen-2-yl)borane, a partially fluorinated boron lewis acid with fluorination distal to the boron atom Organometallics. 33: 1108-1111. DOI: 10.1021/om500128a  1
2014 Nödling AR, Müther K, Rohde VHG, Hilt G, Oestreich M. Ferrocene-stabilized silicon cations as catalysts for diels-alder reactions: Attempted experimental quantification of lewis acidity and reactIR kinetic analysis Organometallics. 33: 302-308. DOI: 10.1021/om401040y  1
2014 Hennecke U, Rösner C, Wald T, Robert T, Oestreich M. Addition Reactions with Formation of Carbonhalogen Bonds Comprehensive Organic Synthesis: Second Edition. 7: 638-691. DOI: 10.1016/B978-0-08-097742-3.00725-4  1
2014 Simonneau A, Friebel J, Oestreich M. Salt-free preparation of trimethylsilyl ethers by B(C6F 5)3-catalyzed transfer silylation by using a Me 3SiH surrogate European Journal of Organic Chemistry. 2014: 2077-2083. DOI: 10.1002/ejoc.201301840  1
2014 Kandukuri SR, Jiao LY, MacHotta AB, Oestreich M. Diastereotopic group selection in hydroxy-directed intramolecular C-H alkenylation of indole under oxidative palladium(II) catalysis Advanced Synthesis and Catalysis. 356: 1597-1609. DOI: 10.1002/adsc.201301108  1
2013 Hermeke J, Mewald M, Oestreich M. Experimental analysis of the catalytic cycle of the borane-promoted imine reduction with hydrosilanes: spectroscopic detection of unexpected intermediates and a refined mechanism. Journal of the American Chemical Society. 135: 17537-46. PMID 24180217 DOI: 10.1021/ja409344w  1
2013 Müther K, Hrobárik P, Hrobáriková V, Kaupp M, Oestreich M. The family of ferrocene-stabilized silylium ions: synthesis, 29Si NMR characterization, Lewis acidity, substituent scrambling, and quantum-chemical analyses. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 16579-94. PMID 24151198 DOI: 10.1002/chem.201302885  1
2013 Simonneau A, Oestreich M. 3-Silylated cyclohexa-1,4-dienes as precursors for gaseous hydrosilanes: the B(C6 F5)3-catalyzed transfer hydrosilylation of alkenes. Angewandte Chemie (International Ed. in English). 52: 11905-7. PMID 24106061 DOI: 10.1002/anie.201305584  1
2013 Jiao LY, Oestreich M. Oxidative palladium(II)-catalyzed C-7 alkenylation of indolines. Organic Letters. 15: 5374-7. PMID 24102435 DOI: 10.1021/ol402687t  1
2013 Königs CD, Klare HF, Oestreich M. Catalytic 1,4-selective hydrosilylation of pyridines and benzannulated congeners. Angewandte Chemie (International Ed. in English). 52: 10076-9. PMID 23907997 DOI: 10.1002/anie.201305028  1
2013 Stahl T, Müther K, Ohki Y, Tatsumi K, Oestreich M. Catalytic generation of borenium ions by cooperative B-H bond activation: the elusive direct electrophilic borylation of nitrogen heterocycles with pinacolborane. Journal of the American Chemical Society. 135: 10978-81. PMID 23855894 DOI: 10.1021/ja405925w  1
2013 Jiao LY, Oestreich M. Oxidative palladium(II)-catalyzed dehydrogenative C-H/C-H cross-coupling of 2,3-substituted indolines with arenes at the C7 position. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 10845-8. PMID 23821552 DOI: 10.1002/chem.201302140  1
2013 Robert T, Oestreich M. Si-H bond activation: bridging Lewis acid catalysis with Brookhart's iridium(III) pincer complex and B(C6F5)3. Angewandte Chemie (International Ed. in English). 52: 5216-8. PMID 23592517 DOI: 10.1002/anie.201301205  1
2013 Delvos LB, Vyas DJ, Oestreich M. Asymmetric synthesis of α-chiral allylic silanes by enantioconvergent γ-selective copper(I)-catalyzed allylic silylation. Angewandte Chemie (International Ed. in English). 52: 4650-3. PMID 23512610 DOI: 10.1002/anie.201300648  1
2013 Königs CD, Müller MF, Aiguabella N, Klare HF, Oestreich M. Catalytic dehydrogenative Si-N coupling of pyrroles, indoles, carbazoles as well as anilines with hydrosilanes without added base. Chemical Communications (Cambridge, England). 49: 1506-8. PMID 23328998 DOI: 10.1039/c3cc38900f  1
2013 Stahl T, Klare HF, Oestreich M. C(sp3)-F bond activation of CF3-substituted anilines with catalytically generated silicon cations: spectroscopic evidence for a hydride-bridged Ru-S dimer in the catalytic cycle. Journal of the American Chemical Society. 135: 1248-51. PMID 23311960 DOI: 10.1021/ja311398j  1
2013 Oestreich M, Hartmann E, Mewald M. Activation of the Si-B interelement bond: mechanism, catalysis, and synthesis. Chemical Reviews. 113: 402-41. PMID 23163551 DOI: 10.1021/cr3003517  1
2013 Müther K, Mohr J, Oestreich M. Silylium ion promoted reduction of imines with hydrosilanes Organometallics. 32: 6643-6646. DOI: 10.1021/om4002796  1
2013 Stahl T, Klare HFT, Oestreich M. Main-group lewis acids for C-F bond activation Acs Catalysis. 3: 1578-1587. DOI: 10.1021/cs4003244  1
2013 Hazra CK, Irran E, Oestreich M. Regio- and diastereoselective copper(I)-catalyzed allylic substitution of δ-hydroxy allylic chlorides by a silicon nucleophile European Journal of Organic Chemistry. 4903-4908. DOI: 10.1002/ejoc.201300493  1
2013 Weickgenannt A, Oestreich M. The Renaissance of Silicon-Stereogenic Silanes: A Personal Account Asymmetric Synthesis Ii: More Methods and Applications. 35-42. DOI: 10.1002/9783527652235.ch5  1
2012 Mewald M, Oestreich M. Illuminating the mechanism of the borane-catalyzed hydrosilylation of imines with both an axially chiral borane and silane. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 14079-84. PMID 22996207 DOI: 10.1002/chem.201202693  1
2012 Kandukuri SR, Oestreich M. Aerobic palladium(II)-catalyzed dehydrogenation of cyclohexene-1-carbonyl indole amides: an indole-directed aromatization. The Journal of Organic Chemistry. 77: 8750-5. PMID 22950832 DOI: 10.1021/jo301088f  1
2012 Hazra CK, Oestreich M. Copper(I)-catalyzed regio- and chemoselective single and double addition of nucleophilic silicon to propargylic chlorides and phosphates. Organic Letters. 14: 4010-3. PMID 22830994 DOI: 10.1021/ol301827t  1
2012 Königs CD, Klare HF, Ohki Y, Tatsumi K, Oestreich M. Base-free dehydrogenative coupling of enolizable carbonyl compounds with silanes. Organic Letters. 14: 2842-5. PMID 22621382 DOI: 10.1021/ol301089r  1
2012 Hartmann E, Oestreich M. Two-directional desymmetrization by double 1,4-addition of silicon and boron nucleophiles. Organic Letters. 14: 2406-9. PMID 22506869 DOI: 10.1021/ol300832f  1
2012 Schmidt RK, Müther K, Mück-Lichtenfeld C, Grimme S, Oestreich M. Silylium ion-catalyzed challenging Diels-Alder reactions: the danger of hidden proton catalysis with strong Lewis acids. Journal of the American Chemical Society. 134: 4421-8. PMID 22309027 DOI: 10.1021/ja211856m  1
2012 Mewald M, Schiffner JA, Oestreich M. A new direction in C-H alkenylation: silanol as a helping hand. Angewandte Chemie (International Ed. in English). 51: 1763-5. PMID 22250066 DOI: 10.1002/anie.201107859  1
2012 Kandukuri SR, Schiffner JA, Oestreich M. Aerobic palladium(II)-catalyzed 5-endo-trig cyclization: an entry into the diastereoselective C-2 alkenylation of indoles with tri- and tetrasubstituted double bonds. Angewandte Chemie (International Ed. in English). 51: 1265-9. PMID 22213474 DOI: 10.1002/anie.201106927  1
2012 Nie W, Klare HFT, Oestreich M, Fröhlich R, Kehr G, Erker G. Reversible heterolytic Si-H bond activation by an intramolecular frustrated Lewis pair Zeitschrift Fur Naturforschung - Section B Journal of Chemical Sciences. 67: 987-994. DOI: 10.5560/ZNB.2012-0181  1
2012 Weickgenannt A, Mohr J, Oestreich M. Catalytic enantioselective dehydrogenative Si-O coupling of oxime ether-functionalized alcohols Tetrahedron. 68: 3468-3479. DOI: 10.1016/j.tet.2011.06.102  1
2012 Wöste TH, Oestreich M. Hemilabile BINAP(O) as a Chiral Ligand in Desymmetrizing Mizoroki-Heck Cyclizations Chemcatchem. 4: 2096-2101. DOI: 10.1002/cctc.201200300  1
2011 Kleeberg C, Feldmann E, Hartmann E, Vyas DJ, Oestreich M. Copper-catalyzed 1,2-addition of nucleophilic silicon to aldehydes: mechanistic insight and catalytic systems. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 13538-43. PMID 22025369 DOI: 10.1002/chem.201102367  1
2011 Wöste TH, Oestreich M. BINAP versus BINAP(O) in asymmetric intermolecular Mizoroki-Heck reactions: substantial effects on selectivities. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 11914-8. PMID 21898621 DOI: 10.1002/chem.201101695  1
2011 Vyas DJ, Hazra CK, Oestreich M. Copper(I)-catalyzed regioselective propargylic substitution involving Si-B bond activation. Organic Letters. 13: 4462-5. PMID 21786824 DOI: 10.1021/ol201811d  1
2011 Müther K, Fröhlich R, Mück-Lichtenfeld C, Grimme S, Oestreich M. A unique transition metal-stabilized silicon cation. Journal of the American Chemical Society. 133: 12442-4. PMID 21774467 DOI: 10.1021/ja205538t  1
2011 Mewald M, Fröhlich R, Oestreich M. An axially chiral, electron-deficient borane: synthesis, coordination chemistry, Lewis acidity, and reactivity. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 9406-14. PMID 21732446 DOI: 10.1002/chem.201100724  1
2011 Hartmann E, Vyas DJ, Oestreich M. Enantioselective formal hydration of α,β-unsaturated acceptors: asymmetric conjugate addition of silicon and boron nucleophiles. Chemical Communications (Cambridge, England). 47: 7917-32. PMID 21528142 DOI: 10.1039/c1cc10528k  1
2011 Vyas DJ, Fröhlich R, Oestreich M. Activation of the Si-B linkage: copper-catalyzed addition of nucleophilic silicon to imines. Organic Letters. 13: 2094-7. PMID 21417305 DOI: 10.1021/ol200509c  1
2011 Klare HF, Oestreich M, Ito J, Nishiyama H, Ohki Y, Tatsumi K. Cooperative catalytic activation of Si-H bonds by a polar Ru-S bond: regioselective low-temperature C-H silylation of indoles under neutral conditions by a Friedel-Crafts mechanism. Journal of the American Chemical Society. 133: 3312-5. PMID 21341748 DOI: 10.1021/ja111483r  1
2011 Müther K, Oestreich M. Self-regeneration of a silylium ion catalyst in carbonyl reduction. Chemical Communications (Cambridge, England). 47: 334-6. PMID 20737081 DOI: 10.1039/c0cc02139c  1
2011 Königs CDF, Oestreich M. Shortened synthesis of a silicon-stereogenic cyclic silane Synthesis. 2062-2065. DOI: 10.1055/s-0030-1259989  1
2011 Schiffner JA, Oestreich M. All-carbon-substituted quaternary carbon atoms in oxindoles by an aerobic palladium(II)-catalyzed ring closure onto tri- and tetrasubstituted double bonds European Journal of Organic Chemistry. 1148-1154. DOI: 10.1002/ejoc.201001526  1
2011 Weickgenannt A, Oestreich M. A new motif for lewis base catalysis: Asymmetric reduction of β-enamino esters Chemcatchem. 3: 1527-1529. DOI: 10.1002/cctc.201100210  1
2011 Hartmann E, Oestreich M. Si-B bond activation in asymmetric Cu(I) and Rh(I) catalysis Chimica Oggi. 29: 34-36.  1
2010 Vyas DJ, Oestreich M. Copper-catalyzed Si-B bond activation in branched-selective allylic substitution of linear allylic chlorides. Angewandte Chemie (International Ed. in English). 49: 8513-5. PMID 20836116 DOI: 10.1002/anie.201004658  1
2010 Vyas DJ, Fröhlich R, Oestreich M. Stereochemical surprises in the Lewis acid-mediated allylation of isatins. The Journal of Organic Chemistry. 75: 6720-3. PMID 20825233 DOI: 10.1021/jo101420e  1
2010 Hartmann E, Oestreich M. Asymmetric conjugate silyl transfer in iterative catalytic sequences: synthesis of the C7-C16 fragment of (+)-neopeltolide. Angewandte Chemie (International Ed. in English). 49: 6195-8. PMID 20648508 DOI: 10.1002/anie.201002916  1
2010 Klare HF, Oestreich M. Silylium ions in catalysis. Dalton Transactions (Cambridge, England : 2003). 39: 9176-84. PMID 20405073 DOI: 10.1039/c003097j  1
2010 Weickgenannt A, Mewald M, Oestreich M. Asymmetric Si-O coupling of alcohols. Organic & Biomolecular Chemistry. 8: 1497-504. PMID 20237658 DOI: 10.1039/b925722e  1
2010 Schiffner JA, Müther K, Oestreich M. Enantioselective conjugate borylation. Angewandte Chemie (International Ed. in English). 49: 1194-6. PMID 20077553 DOI: 10.1002/anie.200906521  1
2010 Vyas DJ, Oestreich M. Expedient access to branched allylic silanes by copper-catalysed allylic substitution of linear allylic halides. Chemical Communications (Cambridge, England). 46: 568-70. PMID 20062864 DOI: 10.1039/b920793g  1
2010 Weickgenannt A, Mewald M, Muesmann TW, Oestreich M. Catalytic asymmetric Si-O coupling of simple achiral silanes and chiral donor-functionalized alcohols. Angewandte Chemie (International Ed. in English). 49: 2223-6. PMID 19967693 DOI: 10.1002/anie.200905561  1
2010 Weickgenannt A, Oestreich M. Silicon- and tin-based cuprates: now catalytic in copper! Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 402-12. PMID 19937624 DOI: 10.1002/chem.200902222  1
2010 Grajewska A, Oestreich M. Base-catalyzed dehydrogenative Si-o coupling of dihydrosilanes: Silylene protection of diols Synlett. 2482-2484. DOI: 10.1055/s-0030-1258055  1
2010 Tappe FMJ, Trepohl VT, Oestreich M. Transition-metal-catalyzed C-P cross-coupling reactions Synthesis. 3037-3062. DOI: 10.1055/s-0030-1257960  1
2010 Mewald M, Weickgenannt A, Fröhlich R, Oestreich M. Expeditious synthesis of TADDOL-derived phosphoramidite and phosphonite ligands Tetrahedron Asymmetry. 21: 1232-1237. DOI: 10.1016/j.tetasy.2010.03.010  1
2010 Bräse S, Würthner F, Lehmann M, Bach T, Müller TJJ, Senge MO, Winkler M, Giernoth R, Ditrich K, Oestreich M, Straub BF, Schröder D, Gschwind R, Schreiner PR, Breinbauer R, et al. Organic chemistry 2009 | Organische Chemie 2009 Nachrichten Aus Der Chemie. 58: 267-299. DOI: 10.1002/nadc.201068299  1
2010 Schiffner JA, Wöste TH, Oestreich M. Enantioselective Fujiwara-Moritani indole and pyrrole annulations catalyzed by chiral palladium(II)-NicOx complexes European Journal of Organic Chemistry. 174-182. DOI: 10.1002/ejoc.200901129  1
2009 Klare HF, Bergander K, Oestreich M. Taming the silylium ion for low-temperature Diels-Alder reactions. Angewandte Chemie (International Ed. in English). 48: 9077-9. PMID 19862787 DOI: 10.1002/anie.200904520  1
2009 Steves A, Oestreich M. Facile preparation of CF3-substituted carbinols with an azine donor and subsequent kinetic resolution through stereoselective Si-O coupling. Organic & Biomolecular Chemistry. 7: 4464-9. PMID 19830296 DOI: 10.1039/b911534j  1
2009 Schmidtmann ES, Oestreich M. Enantiospecific synthesis and allylation of all-carbon-substituted alpha-chiral allylic stannanes. Angewandte Chemie (International Ed. in English). 48: 4634-8. PMID 19437529 DOI: 10.1002/anie.200901384  1
2009 Klare HF, Oestreich M. Asymmetric ring-closing metathesis with a twist. Angewandte Chemie (International Ed. in English). 48: 2085-9. PMID 19199310 DOI: 10.1002/anie.200806254  1
2009 Trepohl VT, Mori S, Itami K, Oestreich M. Palladium(II)-catalyzed conjugate phosphination of electron-deficient acceptors. Organic Letters. 11: 1091-4. PMID 19191507 DOI: 10.1021/ol8028466  1
2009 Weickgenannt A, Oestreich M. Potassium tert-butoxide-catalyzed dehydrogenative Si-O coupling: reactivity pattern and mechanism of an underappreciated alcohol protection. Chemistry, An Asian Journal. 4: 406-10. PMID 19153976 DOI: 10.1002/asia.200800426  1
2009 Trepohl VT, Fröhlich R, Oestreich M. Conjugate phosphination of cyclic and acyclic acceptors using Rh(I)-phosphine or Rh(I)-carbene complexes. Probing the mechanism with chirality at the silicon atom or the phosphorus atom of the Si-P reagent Tetrahedron. 65: 6510-6518. DOI: 10.1016/j.tet.2009.04.038  1
2009 Walter C, Fröhlich R, Oestreich M. Rhodium(I)-catalyzed enantioselective 1,4-addition of nucleophilic silicon Tetrahedron. 65: 5513-5520. DOI: 10.1016/j.tet.2009.01.111  1
2009 Bräse S, Würthner F, Tschierske C, Bach T, Merkul E, Müller TJJ, Winkler M, Giernoth R, Ditrich K, Oestreich M, Straub BF, Muñiz K, Schröder D, Gschwind R, Schreiner PR, et al. Organic chemistry 2008 | Organische Chemie 2008 Nachrichten Aus Der Chemie. 57: 252-277. DOI: 10.1002/nadc.200960646  1
2009 Hog DT, Oestreich M. B(C6F5)3-Catalyzed reduction of ketones and imines using silicon-stereogenic silanes: Stereoinduction by single-point binding European Journal of Organic Chemistry. 5047-5056. DOI: 10.1002/ejoc.200900796  1
2009 Trepohl VT, Oestreich M. Palladium-Catalyzed Arylation Reactions of Alkenes (Mizoroki-Heck Reaction and Related Processes) Modern Arylation Methods. 221-269. DOI: 10.1002/9783527627325.ch7  1
2009 Machotta AB, Oestreich M. Formation of Carbocycles The Mizoroki-Heck Reaction. 179-213. DOI: 10.1002/9780470716076.ch5  1
2008 Rendler S, Plefka O, Karatas B, Auer G, Fröhlich R, Mück-Lichtenfeld C, Grimme S, Oestreich M. 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. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 11512-28. PMID 19021177 DOI: 10.1002/chem.200801377  1
2008 Rendler S, Oestreich M. Conclusive evidence for an S(N)2-Si mechanism in the B(C6F5)3-catalyzed hydrosilylation of carbonyl compounds: implications for the related hydrogenation. Angewandte Chemie (International Ed. in English). 47: 5997-6000. PMID 18613156 DOI: 10.1002/anie.200801675  1
2008 Walter C, Oestreich M. Catalytic asymmetric C-Si bond formation to acyclic alpha,beta-unsaturated acceptors by Rh(I)-catalyzed conjugate silyl transfer using a Si-B linkage. Angewandte Chemie (International Ed. in English). 47: 3818-20. PMID 18389510 DOI: 10.1002/anie.200800361  1
2008 Karatas B, Rendler S, Fröhlich R, Oestreich M. Kinetic resolution of donor-functionalised tertiary alcohols by Cu-H-catalysed stereoselective silylation using a strained silicon-stereogenic silane. Organic & Biomolecular Chemistry. 6: 1435-40. PMID 18385850 DOI: 10.1039/b802186d  1
2008 Rendler S, Oestreich M. Kinetic resolution and desymmetrization by stereoselective silylation of alcohols. Angewandte Chemie (International Ed. in English). 47: 248-50. PMID 17987596 DOI: 10.1002/anie.200704210  1
2008 Schmidt RK, Oestreich M. Transition-metal-free conjugate stannyl transfer to α,β- unsaturated carbonyl and carboxyl compounds in basic aqueous media Synlett. 1690-1692. DOI: 10.1055/s-2008-1078493  1
2008 Schiffner JA, Machotta AB, Oestreich M. A catalytic asymmetric Fujiwara-Moritani cyclization Synlett. 2271-2274. DOI: 10.1055/s-2008-1078271  1
2008 Oestreich M. Directed Mizoroki-Heck reactions Topics in Organometallic Chemistry. 24: 169-192. DOI: 10.1007/3418_2007_063  1
2008 Rendler S, Fröhlich R, Keller M, Oestreich M. Enantio- and diastereotopos differentiation in the palladium(II)-catalyzed hydrosilylation of bicyclo[2.2.1]alkene scaffolds with silicon-stereogenic silanes European Journal of Organic Chemistry. 2582-2591. DOI: 10.1002/ejoc.200800107  1
2008 Rendler S, Oestreich M. Diverse Modes of Silane Activation for the Hydrosilylation of Carbonyl Compounds Modern Reduction Methods. 183-207. DOI: 10.1002/9783527622115.ch8  1
2008 Würthner F, Tschierske C, Bach T, Beifuss U, Müller TJJ, Senge MO, Winkler M, Giernoth R, Ditrich K, Oestreich M, Bisel P, Müller M, Straub BF, Muniz K, Heydt H, et al. Organic chemistry 2007 | Organische Chemie 2007 Nachrichten Aus Der Chemie. 56: 269-294.  1
2007 Klare HF, Oestreich M. Chiral recognition with silicon-stereogenic silanes: remarkable selectivity factors in the kinetic resolution of donor-functionalized alcohols. Angewandte Chemie (International Ed. in English). 46: 9335-8. PMID 17990256 DOI: 10.1002/anie.200703847  1
2007 Machotta AB, Straub BF, Oestreich M. Oxygen donor-mediated equilibration of diastereomeric alkene-palladium(II) intermediates in enantioselective desymmetrizing Heck cyclizations. Journal of the American Chemical Society. 129: 13455-63. PMID 17935323 DOI: 10.1021/ja072571y  1
2007 Trepohl VT, Oestreich M. Rhodium(i)-catalysed conjugate phosphination of cyclic alpha,beta-unsaturated ketones with silylphosphines as masked phosphinides. Chemical Communications (Cambridge, England). 3300-2. PMID 17668107 DOI: 10.1039/b706137d  1
2007 Rendler S, Oestreich M. Conformational rigidity of silicon-stereogenic silanes in asymmetric catalysis: A comparative study. Beilstein Journal of Organic Chemistry. 3: 9. PMID 17288605 DOI: 10.1186/1860-5397-3-9  1
2007 Rendler S, Oestreich M, Butts CP, Lloyd-Jones GC. Intermolecular chirality transfer from silicon to carbon: interrogation of the two-silicon cycle for Pd-catalyzed hydrosilylation by stereoisotopochemical crossover. Journal of the American Chemical Society. 129: 502-3. PMID 17227008 DOI: 10.1021/ja067780h  1
2007 Rendler S, Oestreich M. Polishing a diamond in the rough: "Cu--H" catalysis with silanes. Angewandte Chemie (International Ed. in English). 46: 498-504. PMID 17072922 DOI: 10.1002/anie.200602668  1
2007 Oestreich M. Silicon-stereogenic silanes in asymmetric catalysis Synlett. 1629-1643. DOI: 10.1055/s-2007-980385  1
2007 Krüger A, Würthner F, Beifuss U, Senge MO, Müller TJJ, Albrecht M, Bach T, Tschierske C, Heydt H, Härtung J, Bucher G, Straub BF, Muniz K, Ditrich K, Giernoth R, ... Oestreich M, et al. Organic chemistry 2006 | Organische Chemie 2006 Nachrichten Aus Der Chemie. 55: 252-275.  1
2006 Schmidtmann ES, Oestreich M. Mechanistic insight into copper-catalysed allylic substitutions with bis(triorganosilyl) zincs. Enantiospecific preparation of alpha-chiral silanes. Chemical Communications (Cambridge, England). 3643-5. PMID 17047792 DOI: 10.1039/b606589a  1
2006 Walter C, Auer G, Oestreich M. Rhodium-catalyzed enantioselective conjugate silyl transfer: 1,4-addition of silyl boronic esters to cyclic enones and lactones. Angewandte Chemie (International Ed. in English). 45: 5675-7. PMID 16858702 DOI: 10.1002/anie.200601747  1
2006 Auer G, Oestreich M. Silylzincation of carbon-carbon multiple bonds revisited. Chemical Communications (Cambridge, England). 311-3. PMID 16391744 DOI: 10.1039/b513528a  1
2006 Oestreich M, Sempere-Culler F, Machotta AB. An enantioselective access to an anthracycline AB synthon by a desymmetrizing Heck cyclization Synlett. 2965-2968. DOI: 10.1055/s-2006-944193  1
2006 Auer G, Weiner B, Oestreich M. Copper-free and copper-promoted conjugate addition reactions of bis(triorganosilyl) zincs and tris(triorganosilyl) zincates Synthesis. 2113-2116. DOI: 10.1055/s-2006-942405  1
2006 Rendler S, Auer G, Keller M, Oestreich M. Preparation of a privileged silicon-stereogenic silane: Classical versus kinetic resolution Advanced Synthesis and Catalysis. 348: 1171-1182. DOI: 10.1002/adsc.200606071  1
2006 Würthner F, Tschierske C, Krüger A, Ditrich K, Pfau R, Priepke H, Breinbauer R, Wagenknecht HA, Dräger G, Kirschning A, Sewald N, Beifuss U, Senge MO, Müller TJJ, Schreiner PR, ... ... Oestreich M, et al. Organic chemistry 2005 | Organische chemie 2005 Nachrichten Aus Der Chemie. 54: 241-264.  0.56
2005 Rendler S, Auer G, Oestreich M. Kinetic resolution of chiral secondary alcohols by dehydrogenative coupling with recyclable silicon-stereogenic silanes. Angewandte Chemie (International Ed. in English). 44: 7620-4. PMID 16252303 DOI: 10.1002/anie.200502631  1
2005 Oestreich M, Rendler S. "True" chirality transfer from silicon to carbon: asymmetric amplification in a reagent-controlled palladium-catalyzed hydrosilylation. Angewandte Chemie (International Ed. in English). 44: 1661-4. PMID 15742322 DOI: 10.1002/anie.200462355  1
2005 Rendler S, Oestreich M. Hypervalent silicon as a reactive site in selective bond-forming processes Synthesis. 1727-1747. DOI: 10.1055/s-2005-869949  1
2005 Oestreich M. Neighbouring-group effects in Heck reactions European Journal of Organic Chemistry. 783-792. DOI: 10.1002/ejoc.200400711  1
2005 Oestreich M, Auer G. Practical synthesis of allylic silanes from allylic esters and carbamates by stereoselective copper-catalyzed allylic substitution reactions Advanced Synthesis and Catalysis. 347: 637-640. DOI: 10.1002/adsc.200404381  1
2004 Oestreich M, Sempere-Culler F, Machotta AB. Catalytic desymmetrizing intramolecular Heck reaction: evidence for an unusual hydroxy-directed migratory insertion. Angewandte Chemie (International Ed. in English). 44: 149-52. PMID 15599903 DOI: 10.1002/anie.200460921  1
2004 Oestreich M, Sempere-Culler F. Facile protocol for the highly regioselective and stereodivergent synthesis of substituted bishomoallylic alcohols from esters. Chemical Communications (Cambridge, England). 692-3. PMID 15010784 DOI: 10.1039/b315758j  1
2004 Oestreich M, Weiner B. Copper-catalyzed conjugate addition of a bis(triorganosilyl) zinc and a methyl(triorganosilyl) magnesium Synlett. 2139-2142. DOI: 10.1055/s-2004-831331  1
2004 Oestreich M, Auer G, Keller M. On the mechanism of the reductive metallation of asymmetrically substituted silyl chlorides European Journal of Organic Chemistry. 184-195. DOI: 10.1002/ejoc.200400622  1
2004 Oestreich M. Ways to (-)-galanthamine | Wege zu (-)-Galanthamin Nachrichten Aus Der Chemie. 52: 688-691.  1
2004 Oestreich M. A new iron in the fire | Ein neues eisen im feuer Nachrichten Aus Der Chemie. 52: 446-449.  1
2003 Dounay AB, Hatanaka K, Kodanko JJ, Oestreich M, Overman LE, Pfeifer LA, Weiss MM. Catalytic asymmetric synthesis of quaternary carbons bearing two aryl substituents. Enantioselective synthesis of 3-alkyl-3-aryl oxindoles by catalytic asymmetric intramolecular heck reactions. Journal of the American Chemical Society. 125: 6261-71. PMID 12785859 DOI: 10.1021/ja034525d  1
2001 Oestreich M, Dennison PR, Kodanko JJ, Overman LE. Thwarting β-Hydride Elimination: Capture of the Alkylpalladium Intermediate of an Asymmetric Intramolecular Heck Reaction. Angewandte Chemie (International Ed. in English). 40: 1439-1442. PMID 29712379 DOI: 10.1002/1521-3773(20010417)40:8<1439::AID-ANIE1439>3.0.CO;2-F  1
2001 Oestreich M, Dennison PR, Kodanko JJ, Overman LE. Thwarting beta-Hydride Elimination: Capture of the Alkylpalladium Intermediate of an Asymmetric Intramolecular Heck Reaction This research was supported by the National Institutes of Health (grant GM-12389). M.O. thanks the Deutsche Forschungsgemeinschaft (DFG) for an Emmy Noether fellowship (Oe 249/1-1). NMR and mass spectra were determined at the University of California, Irvine with instruments purchased with the assistance of the NSF and NIH shared instrumentation programs. We are grateful to Dr. Joseph W. Ziller and Dr. John Greaves for their assistance with X-ray structure and mass spectrometric analyses. Angewandte Chemie (International Ed. in English). 40: 1439-1442. PMID 11317296 DOI: 10.1002/1521-3773(20010417)40:8<1439::AID-ANIE1439>3.0.CO;2-F  1
2000 Boudier A, Darcel C, Flachsmann F, Micouin L, Oestreich M, Knochel P. Stereoselective preparation and reactions of configurationally defined dialkylzinc compounds Chemistry (Weinheim An Der Bergstrasse, Germany). 6: 2748-61. PMID 10985723 DOI: 10.1002/1521-3765(20000804)6:15<2748::AID-CHEM2748>3.0.CO;2-Q  1
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