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

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Year Citation  Score
2022 Peng Y, Oestreich M. B(CF)-Catalyzed Reductive Denitrogenation of Benzonitrile Derivatives. Organic Letters. 24: 2940-2943. PMID 35417183 DOI: 10.1021/acs.orglett.2c01003  0.48
2022 He T, Qu ZW, Klare HFT, Grimme S, Oestreich M. Intermolecular Carbosilylation of α-Olefins with C(sp3)-C(sp) Bond Formation Involving Silylium-Ion Regeneration. Angewandte Chemie (International Ed. in English). PMID 35344257 DOI: 10.1002/anie.202203347  0.606
2022 Xie K, Oestreich M. Decarbonylative Transfer Hydrochlorination of Alkenes and Alkynes Based on a B(C F ) -Initiated Grob Fragmentation. Angewandte Chemie (International Ed. in English). e202203692. PMID 35325506 DOI: 10.1002/anie.202203692  0.615
2022 He T, Klare HFT, Oestreich M. Perdeuteration of Deactivated Aryl Halides by H/D Exchange under Superelectrophile Catalysis. Journal of the American Chemical Society. PMID 35258291 DOI: 10.1021/jacs.2c00080  0.441
2022 Rej S, Klare HFT, Oestreich M. Silylium-Ion-Promoted Hydrosilylation of Aryl-Substituted Allenes: Interception by Cyclization of the Allyl-Cation Intermediate. Organic Letters. 24: 1346-1350. PMID 35113570 DOI: 10.1021/acs.orglett.2c00011  0.809
2021 Weidkamp AJ, Oestreich M. Metal-free transfer hydrochlorination of internal C-C triple bonds with a bicyclo[3.1.0]hexane-based surrogate releasing two molecules of hydrogen chloride. Chemical Communications (Cambridge, England). PMID 34950942 DOI: 10.1039/d1cc06591b  0.803
2021 Gao H, Müller R, Irran E, Klare HFT, Kaupp M, Oestreich M. Competition for Hydride between Silicon and Boron: Synthesis and Characterization of a Hydroborane-Stabilized Silylium Ion. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34918852 DOI: 10.1002/chem.202104464  0.807
2021 Klare HFT, Oestreich M. The Power of the Proton: From Superacidic Media to Superelectrophile Catalysis. Journal of the American Chemical Society. PMID 34520196 DOI: 10.1021/jacs.1c07614  0.614
2021 Cui M, Oestreich M. Synthesis of Silylated Cyclobutanone and Cyclobutene Derivatives Involving 1,4-Addition of Zinc-Based Silicon Nucleophiles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34490934 DOI: 10.1002/chem.202102993  0.556
2021 Zhang L, Oestreich M. Nickel-Catalyzed Reductive C(sp3)-Si Cross-Coupling of α-Cyano Alkyl Electrophiles and Chlorosilanes. Angewandte Chemie (International Ed. in English). PMID 34213049 DOI: 10.1002/anie.202107492  0.561
2021 Long PW, Oestreich M. B(CF)-Catalyzed Diastereoselective Formal (4 + 1)-Cycloaddition of Vinylcyclopropanes and EtSiH. Organic Letters. PMID 34076451 DOI: 10.1021/acs.orglett.1c01565  0.311
2021 Finck L, Oestreich M. Transition-Metal-Free Coupling of Polyfluorinated Arenes and Functionalized, Masked Aryl Nucleophiles. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 34014007 DOI: 10.1002/chem.202101731  0.817
2021 Klare HFT, Albers L, Süsse L, Keess S, Müller T, Oestreich M. Silylium Ions: From Elusive Reactive Intermediates to Potent Catalysts. Chemical Reviews. PMID 33861564 DOI: 10.1021/acs.chemrev.0c00855  0.806
2021 Roy A, Oestreich M. Metal-Free Hydrosilylation of Ketenes with Silicon Electrophiles: Access to Fully Substituted Aldehyde-Derived Silyl Enol Ethers. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33825237 DOI: 10.1002/chem.202100877  0.709
2021 Kranidiotis-Hisatomi N, Yi H, Oestreich M. Enantio- and Regioconvergent Nickel-Catalyzed C(sp3)-C(sp3) Cross-Coupling of Allylic Electrophiles Steered by a Silyl Group. Angewandte Chemie (International Ed. in English). PMID 33822445 DOI: 10.1002/anie.202102233  0.815
2021 Fang H, Xie K, Kemper S, Oestreich M. Consecutive β,β'-Selective C(sp3)-H Silylation of Tertiary Amines with Dihydrosilanes Catalyzed by B(C6F5)3. Angewandte Chemie (International Ed. in English). PMID 33604987 DOI: 10.1002/anie.202016664  0.824
2021 Roy A, Oestreich M. At Long Last: The Me Si Group as a Masked Alcohol. Angewandte Chemie (International Ed. in English). PMID 33496981 DOI: 10.1002/anie.202017157  0.67
2020 He T, Wang G, Long PW, Kemper S, Irran E, Klare HFT, Oestreich M. Intramolecular Friedel-Crafts alkylation with a silylium-ion-activated cyclopropyl group: formation of tricyclic ring systems from benzyl-substituted vinylcyclopropanes and hydrosilanes. Chemical Science. 12: 569-575. PMID 34163787 DOI: 10.1039/d0sc05553k  0.769
2020 Fang H, Oestreich M. Defunctionalisation catalysed by boron Lewis acids. Chemical Science. 11: 12604-12615. PMID 34094457 DOI: 10.1039/d0sc03712e  0.811
2020 Papadopulu Z, Oestreich M. Kinetic Resolution of Neopentylic Secondary Alcohols by Cu-H-Catalyzed Enantioselective Silylation with Hydrosilanes. Organic Letters. PMID 33356324 DOI: 10.1021/acs.orglett.0c03943  0.8
2020 Feng JJ, Mao W, Zhang L, Oestreich M. Activation of the Si-B interelement bond related to catalysis. Chemical Society Reviews. PMID 33325936 DOI: 10.1039/d0cs00965b  0.804
2020 Seliger J, Oestreich M. Dynamic Kinetic Resolution of Alcohols by Enantioselective Silylation Enabled by Two Orthogonal Transition-Metal Catalysts. Angewandte Chemie (International Ed. in English). PMID 33107692 DOI: 10.1002/anie.202010484  0.808
2020 Mao W, Oestreich M. Enantioselective Synthesis of α-Chiral Propargylic Silanes by Copper-Catalyzed 1,4-Selective Addition of Silicon Nucleophiles to Enyne-Type α,β,γ,δ-Unsaturated Acceptors. Organic Letters. PMID 33021804 DOI: 10.1021/acs.orglett.0c03046  0.719
2020 Long PW, He T, Oestreich M. B(CF)-Catalyzed Hydrosilylation of Vinylcyclopropanes. Organic Letters. PMID 32903017 DOI: 10.1021/Acs.Orglett.0C02751  0.818
2020 Chen W, Fang H, Xie K, Oestreich M. The Cyclohexa-2,5-dienyl Group as a Placeholder for Hydrogen: Organocatalytic Michael Addition of an Acetaldehyde Surrogate. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32808731 DOI: 10.1002/Chem.202003764  0.818
2020 Xue W, Oestreich M. Beyond Carbon: Enantioselective and Enantiospecific Reactions with Catalytically Generated Boryl- and Silylcopper Intermediates. Acs Central Science. 6: 1070-1081. PMID 32724842 DOI: 10.1021/Acscentsci.0C00738  0.78
2020 Cui M, Oestreich M. Copper-Catalyzed Enantioselective and -Selective Addition of Silicon Nucleophiles to 7-Oxa- and 7-Azabenzonorbornadiene Derivatives. Organic Letters. PMID 32319297 DOI: 10.1021/Acs.Orglett.0C01170  0.611
2020 Fang H, Oestreich M. Reductive Deamination with Hydrosilanes Catalyzed by B(C6F5)3. Angewandte Chemie (International Ed. in English). PMID 32311213 DOI: 10.1002/Anie.202004651  0.812
2020 He T, Wang G, Bonetti V, Klare HFT, Oestreich M. Silylium-Ion-Promoted (5+1) Cycloaddition of Aryl-Substituted Vinylcyclopropanes and Hydrosilanes Involving Aryl Migration. Angewandte Chemie (International Ed. in English). PMID 32302454 DOI: 10.1002/Anie.202004320  0.817
2020 Wu Q, Roy A, Wang G, Irran E, Klare HFT, Oestreich M. Synthesis of a Counteranion-Stabilized Bis(silylium) Ion. Angewandte Chemie (International Ed. in English). PMID 32216163 DOI: 10.1002/Anie.202003799  0.785
2020 Chauvier C, Finck L, Irran E, Oestreich M. Autocatalytic Carbonyl Arylation through In-Situ Release of Aryl Nucleophiles from N-Aryl-N'-Silyldiazenes. Angewandte Chemie (International Ed. in English). PMID 32030857 DOI: 10.1002/Anie.201916004  0.808
2020 Roy A, Bonetti V, Wang G, Wu Q, Klare HFT, Oestreich M. Silylium-Ion-Promoted Ring-Opening Hydrosilylation and Disilylation of Unactivated Cyclopropanes. Organic Letters. PMID 31951144 DOI: 10.1021/Acs.Orglett.0C00173  0.796
2020 Janssen-Müller D, Oestreich M. Transition-Metal-Like Catalysis with a Main-Group Element: Bismuth-Catalyzed C-F Coupling of Aryl Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 31916671 DOI: 10.1002/Anie.201914729  0.802
2020 Fang H, Oestreich M. Defunctionalisation catalysed by boron Lewis acids Chemical Science. DOI: 10.1039/D0Sc03712E  0.813
2020 Fang H, Oestreich M. Reduktive Desaminierung mit Hydrosilanen katalysiert durch B(C 6 F 5 ) 3 Angewandte Chemie. 132: 11491-11495. DOI: 10.1002/Ange.202004651  0.772
2020 Wu Q, Roy A, Wang G, Irran E, Klare HFT, Oestreich M. Synthese eines gegenanionstabilisierten Bis(silylium)ions Angewandte Chemie. 132: 10609-10613. DOI: 10.1002/Ange.202003799  0.775
2020 Chauvier C, Finck L, Irran E, Oestreich M. Autokatalytische Carbonylarylierung mittels lokaler Freisetzung von Arylnukleophilen ausgehend von N ‐Aryl‐ N ′‐silyldiazenen Angewandte Chemie. 132: 12436-12440. DOI: 10.1002/Ange.201916004  0.753
2019 Feng JJ, Xu Y, Oestreich M. Ligand-controlled diastereodivergent, enantio- and regioselective copper-catalyzed hydroxyalkylboration of 1,3-dienes with ketones. Chemical Science. 10: 9679-9683. PMID 32015801 DOI: 10.1039/C9Sc03531A  0.736
2019 Schulz AC, Frielingsdorf S, Pommerening P, Lauterbach L, Bistoni G, Neese F, Oestreich M, Lenz O. Formyltetrahydrofolate decarbonylase synthesizes the active site CO ligand of O-tolerant [NiFe] hydrogenase. Journal of the American Chemical Society. PMID 31830412 DOI: 10.1021/Jacs.9B11506  0.816
2019 Scharfbier J, Gross BM, Oestreich M. Stereospecific and Chemoselective Copper-Catalyzed Deaminative Silylation of Benzylic Ammonium Triflates. Angewandte Chemie (International Ed. in English). PMID 31730248 DOI: 10.1002/Anie.201912490  0.832
2019 Fuchs J, Irran E, Hrobárik P, Klare HFT, Oestreich M. Si-H Bond Activation with Bullock's Cationic Tungsten(II) Catalyst: CO as Cooperating Ligand. Journal of the American Chemical Society. PMID 31692343 DOI: 10.1021/Jacs.9B10304  0.799
2019 Kaicharla T, Zimmermann BM, Oestreich M, Teichert JF. Using alcohols as simple H-equivalents for copper-catalysed transfer semihydrogenations of alkynes. Chemical Communications (Cambridge, England). PMID 31638107 DOI: 10.1039/C9Cc06637C  0.702
2019 Wu Q, Roy A, Irran E, Qu ZW, Grimme S, Klare H, Oestreich M. Catalytic Difunctionalization of Unactivated Alkenes with Unreactive Hexamethyldisilane through Regeneration of Silylium Ions. Angewandte Chemie (International Ed. in English). PMID 31566863 DOI: 10.1002/Anie.201911282  0.822
2019 Zhang L, Oestreich M. Copper-Catalyzed Enantio- and Diastereoselective Addition of Silicon Nucleophiles to 3,3-Disubstituted Cyclopropenes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31531992 DOI: 10.1002/Chem.201904272  0.626
2019 Walker JCL, Oestreich M. Lewis Acid-Catalyzed Transfer Hydromethallylation for the Construction of Quaternary Carbon Centers. Angewandte Chemie (International Ed. in English). PMID 31449730 DOI: 10.1002/Anie.201909852  0.823
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  0.757
2019 Chen W, Oestreich M. Metal-Free Transfer Hydrobromination of C-C Triple Bonds. Organic Letters. PMID 31150253 DOI: 10.1021/Acs.Orglett.9B01431  0.601
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  0.829
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  0.679
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  0.735
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  0.795
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  0.583
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  0.827
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  0.775
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  0.792
2019 Walker JCL, Oestreich M. Ionic Transfer Reactions with Cyclohexadiene-Based Surrogates Synlett. 30: 2216-2232. DOI: 10.1055/S-0039-1690233  0.794
2019 Shaykhutdinova P, Oestreich M. Further Structural Modification of Sulfur-Stabilized Silicon Cations with Binaphthyl Backbones Synthesis. 51: 2221-2229. DOI: 10.1055/S-0037-1610697  0.827
2019 Shaykhutdinova P, Oestreich M. Further Structural Modification of Sulfur-Stabilized Silicon Cations with Binaphthyl Backbones Synthesis. 51: 2221-2229. DOI: 10.1055/s-0037-1610697  0.326
2019 Chauvier C, Finck L, Hecht S, Oestreich M. General Synthesis and Optical Properties of N-Aryl-N′-Silyldiazenes Organometallics. 38: 4679-4686. DOI: 10.1021/Acs.Organomet.9B00654  0.789
2019 Süsse L, LaFortune JHW, Stephan DW, Oestreich M. Axially Chiral, Electrophilic Fluorophosphonium Cations: Synthesis, Lewis Acidity, and Reactivity in the Hydrosilylation of Ketones Organometallics. 38: 712-721. DOI: 10.1021/Acs.Organomet.8B00912  0.81
2019 Pommerening P, Oestreich M. Chiral Modification of the Tetrakis(pentafluorophenyl)borate Anion with Myrtanyl Groups European Journal of Organic Chemistry. 2019: 7240-7246. DOI: 10.1002/Ejoc.201901434  0.79
2019 Scharfbier J, Gross BM, Oestreich M. Stereospezifische und chemoselektive kupferkatalysierte, deaminierende Silylierung von Benzylammoniumtriflaten Angewandte Chemie. 132: 1593-1596. DOI: 10.1002/Ange.201912490  0.77
2019 Wu Q, Roy A, Irran E, Qu Z, Grimme S, Klare HFT, Oestreich M. Katalytische Difunktionalisierung von nichtaktivierten Alkenen mit reaktionsträgem Hexamethyldisilan durch Neubildung von Silyliumionen Angewandte Chemie. 131: 17468-17472. DOI: 10.1002/Ange.201911282  0.769
2019 Walker JCL, Oestreich M. Lewis Säure‐katalysierte Transferhydromethallylierung für den Aufbau quartärer Kohlenstoffzentren Angewandte Chemie. 131: 15530-15534. DOI: 10.1002/Ange.201909852  0.786
2019 Mao W, Xue W, Irran E, Oestreich M. Kupferkatalysierte regio‐ und enantioselektive Addition von Silicium‐Grignard‐Reagenzien an durch Azaarylgruppen aktivierte Alkene Angewandte Chemie. 131: 10833-10836. DOI: 10.1002/Ange.201905934  0.817
2019 Mao W, Xue W, Irran E, Oestreich M. Kupferkatalysierte regio‐ und enantioselektive Addition von Silicium‐Grignard‐Reagenzien an durch Azaarylgruppen aktivierte Alkene Angewandte Chemie. 131: 10833-10836. DOI: 10.1002/ange.201905934  0.817
2019 Feng J, Oestreich M. Tertiäre α‐Silylalkohole mittels diastereoselektiver Kupplung von 1,3‐Dienen und Acylsilanen, eingeleitet durch enantioselektive kupferkatalysierte Borylierung Angewandte Chemie. 131: 8295-8299. DOI: 10.1002/Ange.201903174  0.665
2019 Xue W, Mao W, Zhang L, Oestreich M. Gegensätzliche Reaktionsweisen magnesium‐ und zinkbasierter Germaniumnukleophile in der C(sp 3 )‐Ge‐Kreuzkupplung mit Alkylelektrophilen Angewandte Chemie. 131: 6506-6509. DOI: 10.1002/Ange.201901860  0.779
2019 Yi H, Mao W, Oestreich M. Enantioselektiver Aufbau von α‐chiralen Silanen durch nickelkatalysierte C(sp 3 )‐C(sp 3 )‐Kreuzkupplung Angewandte Chemie. 131: 3613-3616. DOI: 10.1002/Ange.201814340  0.733
2019 Orecchia P, Yuan W, Oestreich M. Bor-Lewis-Säure-katalysierte Transferhydrocyanierung α- und α,β-substituierter Styrole Angewandte Chemie. 131: 3617-3621. DOI: 10.1002/Ange.201813853  0.73
2019 Seliger J, Dong X, Oestreich M. Kinetische Racematspaltung tertiärer Propargylalkohole durch enantioselektive Cu-H-katalysierte Si-O-Kupplung Angewandte Chemie. 131: 1991-1996. DOI: 10.1002/Ange.201813229  0.779
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  0.806
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  0.817
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  0.589
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  0.805
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  0.84
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  0.815
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  0.744
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  0.688
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  0.828
2018 Xue W, Shishido R, Oestreich M. Bench-Stable Stock Solutions of Silicon Grignard Reagents: Application to Iron- and Cobalt-Catalyzed Radical C(sp3)-Si Cross-Coupling Reactions. Angewandte Chemie (International Ed. in English). PMID 30070420 DOI: 10.1002/Anie.201807640  0.762
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  0.79
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  0.814
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  0.751
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  0.815
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  0.789
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  0.783
2018 Bähr S, Oestreich M. A Neutral Ru(II) Hydride Complex for the Regio- and Chemoselective Reduction of N-Silylpyridinium Ions. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29436732 DOI: 10.1002/Chem.201705899  0.793
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  0.746
2018 Bähr S, Oestreich M. The electrophilic aromatic substitution approach to C–H silylation and C–H borylation Pure and Applied Chemistry. 90: 723-731. DOI: 10.1515/Pac-2017-0902  0.807
2018 Xue W, Oestreich M. Silicon Grignard Reagents as Nucleophiles in Transition-Metal-Catalyzed Allylic Substitution Synthesis. 51: 233-239. DOI: 10.1055/S-0037-1610309  0.767
2018 Xue W, Oestreich M. Silicon Grignard Reagents as Nucleophiles in Transition-Metal-Catalyzed Allylic Substitution Synthesis. 51: 233-239. DOI: 10.1055/s-0037-1610309  0.751
2018 Xue W, Oestreich M. Silicon Grignard Reagents as Nucleophiles in Transition-Metal-Catalyzed Allylic Substitution Synthesis. 51: 233-239. DOI: 10.1055/s-0037-1610309  0.3
2018 Xue W, Oestreich M. Silicon Grignard Reagents as Nucleophiles in Transition-Metal-Catalyzed Allylic Substitution Synthesis. 51: 233-239. DOI: 10.1055/s-0037-1610309  0.3
2018 Bähr S, Xue W, Oestreich M. C(sp3)–Si Cross-Coupling Acs Catalysis. 9: 16-24. DOI: 10.1021/Acscatal.8B04230  0.822
2018 Vogler M, Süsse L, LaFortune JHW, Stephan DW, Oestreich M. Electrophilic Phosphonium Cations as Lewis Acid Catalysts in Diels–Alder Reactions and Nazarov Cyclizations Organometallics. 37: 3303-3313. DOI: 10.1021/Acs.Organomet.8B00496  0.818
2018 Vogler M, Süsse L, LaFortune JHW, Stephan DW, Oestreich M. Electrophilic Phosphonium Cations as Lewis Acid Catalysts in Diels–Alder Reactions and Nazarov Cyclizations Organometallics. 37: 3303-3313. DOI: 10.1021/acs.organomet.8b00496  0.705
2018 Forster F, Rendón López VM, Oestreich M. Z-Selective Hydrostannylation of Terminal and Internal C–C Triple Bonds Initiated by the Trityl Cation Organometallics. 37: 2656-2659. DOI: 10.1021/Acs.Organomet.8B00409  0.74
2018 Yuan W, Smirnov P, Oestreich M. Custom Hydrosilane Synthesis Based on Monosilane Chem. 4: 1443-1450. DOI: 10.1016/J.Chempr.2018.03.017  0.817
2018 Shaykhutdinova P, Kemper S, Oestreich M. 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 European Journal of Organic Chemistry. 2018: 2896-2901. DOI: 10.1002/Ejoc.201800434  0.823
2018 Shaykhutdinova P, Kemper S, Oestreich M. 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 European Journal of Organic Chemistry. 2018: 2896-2901. DOI: 10.1002/ejoc.201800434  0.31
2018 Pommerening P, Stahl T, Oestreich M. Direct Acetophenone-Acetophenone Crossed Aldol Reaction and Aldol Self-Reaction Promoted by a Tethered Ru-S Complex European Journal of Organic Chemistry. 2018: 2290-2293. DOI: 10.1002/Ejoc.201800132  0.792
2018 Dong X, Kita Y, Oestreich M. Inside Back Cover: Kinetic Resolution of α‐Hydroxy‐Substituted Oxime Ethers by Enantioselective Cu−H‐Catalyzed Si−O Coupling (Angew. Chem. Int. Ed. 33/2018) Angewandte Chemie International Edition. 57: 10771-10771. DOI: 10.1002/Anie.201806828  0.758
2018 Merk A, Großekappenberg H, Schmidtmann M, Luecke M, Lorent C, Driess M, Oestreich M, Klare HFT, Müller T. Einelektronenübertragungsreaktionen in frustrierten und klassischen Silyliumion/Phosphan‐Lewis‐Paaren Angewandte Chemie. 130: 15487-15492. DOI: 10.1002/Ange.201808922  0.66
2018 Xue W, Shishido R, Oestreich M. Stabile Stammlösungen von Silicium-Grignard-Reagenzien: Anwendung in eisen- und cobaltkatalysierten radikalischen C(sp3 )-Si-Kreuzkupplungsreaktionen Angewandte Chemie. 130: 12318-12322. DOI: 10.1002/Ange.201807640  0.728
2018 Dong X, Kita Y, Oestreich M. Innenrücktitelbild: Kinetische Racematspaltung α‐hydroxysubstituierter Oximether durch enantioselektive Cu‐H‐katalysierte Si‐O‐Kupplung (Angew. Chem. 33/2018) Angewandte Chemie. 130: 10933-10933. DOI: 10.1002/Ange.201806828  0.722
2018 Süsse L, Vogler M, Mewald M, Kemper B, Irran E, Oestreich M. Enantioselektive Nazarov-Cyclisierungen, die von einer axial-chiralen, C6 F5 -substituierten Bor-Lewis-Säure katalysiert werden Angewandte Chemie. 130: 11612-11615. DOI: 10.1002/Ange.201806011  0.77
2018 Wu Q, Qu Z, Omann L, Irran E, Klare HFT, Oestreich M. Spaltung nicht aktivierter Si-C(sp3)-Bindungen mit Reedschen Carboransäuren: Bildung bekannter und unbekannter Silyliumionen Angewandte Chemie. 130: 9317-9320. DOI: 10.1002/Ange.201805637  0.791
2018 Omann L, Qu Z, Irran E, Klare HFT, Grimme S, Oestreich M. Elektrophile Formylierung von Aromaten durch silyliumionvermittelte Aktivierung von Kohlenmonoxid Angewandte Chemie. 130: 8433-8437. DOI: 10.1002/Ange.201803181  0.767
2018 Dong X, Kita Y, Oestreich M. Kinetische Racematspaltung α‐hydroxysubstituierter Oximether durch enantioselektive Cu‐H‐katalysierte Si‐O‐Kupplung Angewandte Chemie. 130: 10888-10891. DOI: 10.1002/Ange.201802947  0.732
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  0.827
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  0.808
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  0.804
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  0.81
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  0.767
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  0.769
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  0.799
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  0.557
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  0.832
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  0.734
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  0.818
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  0.754
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  0.829
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  0.817
2017 Oestreich M. Cluster Preface: Silicon in Synthesis and Catalysis Synlett. 28: 2394-2395. DOI: 10.1055/S-0036-1591626  0.374
2017 Porwal D, Oestreich M. B(C6F5)3-Catalyzed Reduction of Sulfoxides and Sulfones to Sulfides with Hydrosilanes Synthesis. 49: 4698-4702. DOI: 10.1055/S-0036-1588476  0.825
2017 Porwal D, Oestreich M. B(C6F5)3-Catalyzed Reduction of Sulfoxides and Sulfones to Sulfides with Hydrosilanes Synthesis. 49: 4698-4702. DOI: 10.1055/s-0036-1588476  0.314
2017 Porwal D, Oestreich M. B(C6F5)3-Catalyzed Reduction of Sulfoxides and Sulfones to Sulfides with Hydrosilanes Synthesis. 49: 4698-4702. DOI: 10.1055/s-0036-1588476  0.314
2017 Porwal D, Oestreich M. B(C6F5)3-Catalyzed Reduction of Sulfoxides and Sulfones to Sulfides with Hydrosilanes Synthesis. 49: 4698-4702. DOI: 10.1055/s-0036-1588476  0.314
2017 Oestreich M, Wübbolt S. Exhaustive Chemoselective Reduction of Nitriles by Catalytic Hydrosilylation Involving Cooperative Si–H Bond Activation Synlett. 28: 2411-2414. DOI: 10.1055/S-0036-1588441  0.813
2017 Fuchs J, Klare HFT, Oestreich M. Two-Silicon Cycle for Carbonyl Hydrosilylation with Nikonov’s Cationic Ruthenium(II) Catalyst Acs Catalysis. 7: 8338-8342. DOI: 10.1021/Acscatal.7B03336  0.794
2017 Bähr S, Ogasawara H, Yamaguchi S, Oestreich M. An Expedient Procedure for the Synthesis of Benzo[4,5]silolo[2,3-b]thiophenes and Related Systems Organometallics. 36: 4013-4019. DOI: 10.1021/Acs.Organomet.7B00619  0.814
2017 Yin Q, Soltani Y, Melen RL, Oestreich M. BArF3-Catalyzed Imine Hydroboration with Pinacolborane Not Requiring the Assistance of an Additional Lewis Base Organometallics. 36: 2381-2384. DOI: 10.1021/Acs.Organomet.7B00381  0.566
2017 Yin Q, Soltani Y, Melen RL, Oestreich M. BArF3-Catalyzed Imine Hydroboration with Pinacolborane Not Requiring the Assistance of an Additional Lewis Base Organometallics. 36: 2381-2384. DOI: 10.1021/Acs.Organomet.7B00381  0.566
2017 Bähr S, Oestreich M. 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. 36: 935-943. DOI: 10.1021/Acs.Organomet.7B00030  0.831
2017 Pommerening P, Mohr J, Friebel J, Oestreich M. Synthesis of a Chiral Borate Counteranion, Its Trityl Salt, and Application Thereof in Lewis-Acid Catalysis European Journal of Organic Chemistry. 2017: 2312-2316. DOI: 10.1002/Ejoc.201700239  0.829
2017 Pommerening P, Mohr J, Friebel J, Oestreich M. Synthesis of a Chiral Borate Counteranion, Its Trityl Salt, and Application Thereof in Lewis-Acid Catalysis European Journal of Organic Chemistry. 2017: 2312-2316. DOI: 10.1002/ejoc.201700239  0.798
2017 Xue W, Oestreich M. Kupferkatalysierte decarboxylierende radikalische Silylierung von redoxaktiven aliphatischen Carbonsäurederivaten Angewandte Chemie. 129: 11808-11811. DOI: 10.1002/Ange.201706611  0.694
2017 Yin Q, Oestreich M. Photokatalyse ermöglicht die akzeptorfreie Dehydrierung von benzanellierten gesättigten Ringen bei Raumtemperatur Angewandte Chemie. 129: 7824-7826. DOI: 10.1002/Ange.201703536  0.509
2017 Chatterjee I, Porwal D, Oestreich M. B(C6F5)3-katalysierte chemoselektive Defunktionalisierung von etherhaltigen primären Alkyltosylaten mit Hydrosilanen Angewandte Chemie. 129: 3438-3441. DOI: 10.1002/Ange.201611813  0.773
2017 Yin Q, Klare HFT, Oestreich M. Katalytische Friedel-Crafts-C-H-Borylierung elektronenreicher Arene: starke Reaktionsbeschleunigung durch Versetzen mit Alkenen Angewandte Chemie. 129: 3766-3771. DOI: 10.1002/Ange.201611536  0.708
2016 Klare HF, Oestreich M. Teaching nature the unnatural. Science (New York, N.Y.). 354: 970. PMID 27884992 DOI: 10.1126/Science.Aal1951  0.636
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  0.826
2016 Bähr S, Oestreich M. Electrophilic Aromatic Substitution with Silicon Electrophiles: Catalytic Friedel-Crafts C-H Silylation. Angewandte Chemie (International Ed. in English). PMID 27762042 DOI: 10.1002/Anie.201608470  0.83
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  0.802
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  0.769
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  0.747
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  0.813
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  0.742
2016 Süsse L, Hermeke J, Oestreich M. The Asymmetric Piers Hydrosilylation. Journal of the American Chemical Society. PMID 27212565 DOI: 10.1021/Jacs.6B03443  0.824
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  0.666
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  0.827
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  0.77
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  0.744
2016 Oestreich M, Perez-Luna A, Fopp C, Isaac K, Romain E, Chemla F, Ferreira F, Jackowski O. Stereodivergent Synthesis of β-Heteroatom-Substituted Vinyl­silanes by Sequential Silylzincation–Copper(I)-Mediated Electrophilic­ Substitution Synthesis. 49: 724-735. DOI: 10.1055/S-0036-1588106  0.825
2016 Yamamoto H, Sai M, Süsse L, Hermeke J, Oestreich M. Axially Chiral Boron Catalyst for Asymmetric Piers Hydrosilylation Synfacts. 12: 833-833. DOI: 10.1055/S-0035-1562661  0.325
2016 Knochel P, Ziegler D, Fopp C, Romain E, Isaac K, Chemla F, Ferreira F, Jackowski O, Oestreich M, Perez-Luna A. Stereoselective Silylzincation of Alkynes Synfacts. 12: 729-729. DOI: 10.1055/S-0035-1562325  0.823
2016 Oestreich M, Scharfbier J. Copper-Catalyzed Si–B Bond Activation in the Nucleophilic Substitution of Primary Aliphatic Triflates Synlett. 27: 1274-1276. DOI: 10.1055/S-0035-1561407  0.81
2016 Omann L, Oestreich M. Catalytic Access to Indole-Fused Benzosiloles by 2-Fold Electrophilic C–H Silylation with Dihydrosilanes Organometallics. 36: 767-776. DOI: 10.1021/Acs.Organomet.6B00801  0.822
2016 Shaykhutdinova P, Oestreich M. Enantioselective Diels–Alder Reactions of Cyclohexa-1,3-diene and Chalcones Catalyzed by Intramolecular Silicon–Sulfur Lewis Pairs as Chiral Lewis Acids Organometallics. 35: 2768-2771. DOI: 10.1021/Acs.Organomet.6B00548  0.835
2016 Smirnov P, Oestreich M. Merging Platinum-Catalyzed Alkene Hydrosilylation with SiH4 Surrogates: Salt-Free Preparation of Trihydrosilanes Organometallics. 35: 2433-2434. DOI: 10.1021/Acs.Organomet.6B00505  0.832
2016 Mehta M, Garcia De La Arada I, Perez M, Porwal D, Oestreich M, Stephan DW. Metal-Free Phosphine Oxide Reductions Catalyzed by B(C6F5)3 and Electrophilic Fluorophosphonium Cations Organometallics. 35: 1030-1035. DOI: 10.1021/Acs.Organomet.6B00158  0.797
2016 Bähr S, Simonneau A, Irran E, Oestreich M. An Air-Stable Dimeric Ru–S Complex with an NHC as Ancillary Ligand for Cooperative Si–H Bond Activation Organometallics. 35: 925-928. DOI: 10.1021/Acs.Organomet.6B00110  0.799
2016 Porwal D, Oestreich M. B(C6F5)3-Catalyzed Reduction of Aromatic and Aliphatic Nitro Groups with Hydrosilanes European Journal of Organic Chemistry. 2016: 3307-3309. DOI: 10.1002/Ejoc.201600556  0.801
2016 Porwal D, Oestreich M. ChemInform Abstract: B(C6F5)3-Catalyzed Reduction of Aromatic and Aliphatic Nitro Groups with Hydrosilanes. Cheminform. 47. DOI: 10.1002/chin.201648033  0.791
2016 Scharfbier J, Oestreich M. ChemInform Abstract: Copper-Catalyzed Si-B Bond Activation in the Nucleophilic Substitution of Primary Aliphatic Triflates. Cheminform. 47. DOI: 10.1002/chin.201639192  0.821
2016 Scharfbier J, Oestreich M. ChemInform Abstract: Copper-Catalyzed Si-B Bond Activation in the Nucleophilic Substitution of Primary Aliphatic Triflates. Cheminform. 47. DOI: 10.1002/chin.201639192  0.821
2016 Scharfbier J, Oestreich M. ChemInform Abstract: Copper-Catalyzed Si-B Bond Activation in the Nucleophilic Substitution of Primary Aliphatic Triflates. Cheminform. 47. DOI: 10.1002/chin.201639192  0.302
2016 Scharfbier J, Oestreich M. ChemInform Abstract: Copper-Catalyzed Si-B Bond Activation in the Nucleophilic Substitution of Primary Aliphatic Triflates. Cheminform. 47. DOI: 10.1002/chin.201639192  0.302
2016 Bähr S, Oestreich M. Elektrophile aromatische Substitution mit Siliciumelektrophilen: die katalytische Friedel-Crafts-C-H-Silylierung Angewandte Chemie. 129: 52-59. DOI: 10.1002/Ange.201608470  0.796
2016 Mohr J, Oestreich M. Ausbalancieren von C=C-Funktionalisierung und C=O-Reduktion in der Cu-H-Katalyse Angewandte Chemie. 128: 12330-12332. DOI: 10.1002/Ange.201606701  0.749
2016 Yin Q, Klare HFT, Oestreich M. Durch Nichtedelmetallsalze ausgelöste Friedel-Crafts-artige intermolekulare C-H-Silylierung von elektronenreichen Arenen Angewandte Chemie. 128: 3256-3260. DOI: 10.1002/Ange.201510469  0.703
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  0.786
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  0.802
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  0.838
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  0.82
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  0.729
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  0.75
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  0.666
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  0.82
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  0.685
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  0.772
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  0.669
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  0.704
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  0.811
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  0.699
2015 Knochel P, Hammann JM, Pareek M, Fallon T, Oestreich M. Platinum-Catalyzed Indolyne Insertion/Cross-Coupling Synfacts. 11: 855-855. DOI: 10.1055/S-0034-1381131  0.381
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  0.823
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  0.73
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  0.836
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  0.316
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  0.717
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  0.458
2015 Oestreich M, Hermeke J, Mohr J. ChemInform Abstract: A Unified Survey of Si-H and H-H Bond Activation Catalyzed by Electron-Deficient Boranes Cheminform. 46: no-no. DOI: 10.1002/chin.201527278  0.794
2015 Fallon T, Oestreich M. Back Cover: A Constellation of Deuterium-Labeled Silanes as a Simple Mechanistic Probe not Requiring Absolute Configuration Determination (Angew. Chem. Int. Ed. 42/2015) Angewandte Chemie International Edition. 54: 12516-12516. DOI: 10.1002/Anie.201508437  0.597
2015 Fallon T, Oestreich M. Rücktitelbild: Eine Mischung deuteriummarkierter Silane als einfache mechanistische Sonde, die ohne Bestimmung von absoluten Konfigurationen auskommt (Angew. Chem. 42/2015) Angewandte Chemie. 127: 12698-12698. DOI: 10.1002/Ange.201508437  0.578
2015 Wübbolt S, Oestreich M. Katalytische elektrophile C-H-Silylierung von Pyridinen ermöglicht durch vorübergehende Aufhebung der Aromatizität Angewandte Chemie. 127: 16103-16106. DOI: 10.1002/Ange.201508181  0.793
2015 Wübbolt S, Oestreich M. Katalytische elektrophile C-H-Silylierung von Pyridinen ermöglicht durch vorübergehende Aufhebung der Aromatizität Angewandte Chemie. 127: 16103-16106. DOI: 10.1002/Ange.201508181  0.793
2015 Chatterjee I, Qu Z, Grimme S, Oestreich M. B(C6F5)3-katalysierter Diwasserstofftransfer von einem ungesättigten Kohlenwasserstoff auf einen anderen Angewandte Chemie. 127: 12326-12330. DOI: 10.1002/Ange.201504941  0.694
2015 Omann L, Oestreich M. Ein katalytischer SEAr-Zugang zu Dibenzosilolen mit Funktionalisierung an beiden Benzolkernen Angewandte Chemie. 127: 10414-10418. DOI: 10.1002/Ange.201504066  0.789
2015 Fallon T, Oestreich M. Eine Mischung deuteriummarkierter Silane als einfache mechanistische Sonde, die ohne Bestimmung von absoluten Konfigurationen auskommt Angewandte Chemie. 127: 12666-12670. DOI: 10.1002/Ange.201500750  0.607
2015 Simonneau A, Oestreich M. Faszinierende Chemie des Wasserstoffatomtransfers auf Alkene inspiriert durch Probleme in Totalsynthesen Angewandte Chemie. 127: 3626-3628. DOI: 10.1002/Ange.201500557  0.654
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  0.651
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  0.806
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  0.781
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  0.811
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  0.81
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  0.477
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  0.831
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  0.811
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  0.828
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  0.401
2014 Oestreich M, Klare H, Müther K, Fröhlich R. Taming Super Lewis Acids for Catalysis: The Family of Ferrocene-Stabilized Silicon Cations Scienceopen Posters. DOI: 10.14293/P2199-8442.1.Sop-Chem.Pmugh7.V1  0.782
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  0.823
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  0.812
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  0.819
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  0.667
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  0.813
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  0.816
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  0.584
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  0.816
2014 Chatterjee I, Oestreich M. B(C6F5)3-katalysierte Transferhydrierung von Iminen und verwandten Heteroaromaten mit Cyclohexa-1,4-dienen als Wasserstoffquelle Angewandte Chemie. 127: 1988-1991. DOI: 10.1002/Ange.201409246  0.631
2014 Mohr J, Oestreich M. B(C6F5)3-katalysierte Hydrierung von Oximethern ohne Spaltung der N-O-Bindung Angewandte Chemie. 126: 13494-13497. DOI: 10.1002/Ange.201407324  0.749
2014 Hensel A, Nagura K, Delvos LB, Oestreich M. Enantioselektive Addition von Siliciumnukleophilen an Aldimine mit einem präformierten NHC-Kupfer(I)-Komplex als Katalysator Angewandte Chemie. 126: 5064-5067. DOI: 10.1002/Ange.201402086  0.791
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  0.8
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  0.835
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  0.81
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  0.706
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  0.657
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  0.655
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  0.816
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  0.63
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  0.63
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  0.839
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  0.784
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  0.783
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  0.812
2013 Müther K, Mohr J, Oestreich M. Silylium ion promoted reduction of imines with hydrosilanes Organometallics. 32: 6643-6646. DOI: 10.1021/Om4002796  0.784
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  0.765
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  0.805
2013 Simonneau A, Oestreich M. 3-Silylierte Cyclohexa-1,4-diene als Vorstufen für gasförmige Hydrosilane: die B(C6F5)3-katalysierte Transferhydrosilylierung von Alkenen Angewandte Chemie. 125: 12121-12124. DOI: 10.1002/Ange.201305584  0.676
2013 Königs CDF, Klare HFT, Oestreich M. Katalytische 1,4-selektive Hydrosilylierung von Pyridinverbindungen und benzanellierten Verwandten Angewandte Chemie. 125: 10260-10263. DOI: 10.1002/Ange.201305028  0.593
2013 Robert T, Oestreich M. Si-H-Bindungsaktivierung: Parallelen der Lewis-Säure-Katalyse mit Brookharts Iridium(III)-Pincerkomplex und B(C6F5)3 Angewandte Chemie. 125: 5324-5326. DOI: 10.1002/Ange.201301205  0.601
2013 Delvos LB, Vyas DJ, Oestreich M. Asymmetrische Synthese α-chiraler Allylsilane durch enantiokonvergente γ-selektive Kupfer(I)-katalysierte allylische Silylierung Angewandte Chemie. 125: 4748-4751. DOI: 10.1002/Ange.201300648  0.783
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  0.746
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  0.822
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  0.829
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  0.806
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  0.693
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  0.643
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  0.817
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  0.784
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  0.819
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  0.656
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  0.811
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  0.793
2012 Mewald M, Schiffner JA, Oestreich M. Ein neuer Weg der C-H-Alkenylierung: Silanol als helfende Hand Angewandte Chemie. 124: 1797-1799. DOI: 10.1002/Ange.201107859  0.778
2012 Mewald M, Schiffner JA, Oestreich M. Ein neuer Weg der C-H-Alkenylierung: Silanol als helfende Hand Angewandte Chemie. 124: 1797-1799. DOI: 10.1002/Ange.201107859  0.778
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  0.766
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  0.802
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  0.825
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  0.801
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  0.806
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  0.745
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  0.652
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  0.686
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  0.793
2011 Königs CDF, Oestreich M. Shortened synthesis of a silicon-stereogenic cyclic silane Synthesis. 2062-2065. DOI: 10.1055/S-0030-1259989  0.397
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  0.753
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  0.773
2011 Kandukuri SR, Schiffner JA, Oestreich M. Aerobe Palladium(II)-katalysierte 5-endo-trig-Cyclisierung als ein Einstieg in die diastereoselektive C-2-Alkenylierung von Indolen mit tri- und tetrasubstituierten Doppelbindungen Angewandte Chemie. 124: 1291-1295. DOI: 10.1002/Ange.201106927  0.783
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  0.648
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  0.622
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  0.611
2010 Klare HF, Oestreich M. Silylium ions in catalysis. Dalton Transactions (Cambridge, England : 2003). 39: 9176-84. PMID 20405073 DOI: 10.1039/C003097J  0.676
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  0.798
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  0.808
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  0.66
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  0.801
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  0.802
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  0.758
2010 Tappe FMJ, Trepohl VT, Oestreich M. Transition-metal-catalyzed C-P cross-coupling reactions Synthesis. 3037-3062. DOI: 10.1055/S-0030-1257960  0.794
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  0.805
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  0.823
2010 Oestreich M, Hoppe D. ChemInform Abstract: Stereospecific Preparation of Highly Enantiomerically Enriched Organomagnesium Reagents Cheminform. 32: no-no. DOI: 10.1002/chin.200136272  0.4
2010 Oestreich M, Hoppe D. ChemInform Abstract: Stereospecific Preparation of Highly Enantiomerically Enriched Organomagnesium Reagents Cheminform. 32: no-no. DOI: 10.1002/chin.200136272  0.4
2010 MICOUIN L, OESTREICH M, KNOCHEL P. ChemInform Abstract: Stereoselective Preparation and Reactions of Cycloalkylzinc Compounds. Cheminform. 28: no-no. DOI: 10.1002/chin.199719092  0.33
2010 Vyas DJ, Oestreich M. Kupferkatalysierte Si-B-Bindungsaktivierung in der verzweigtselektiven allylischen Substitution linearer Allylchloride Angewandte Chemie. 122: 8692-8694. DOI: 10.1002/Ange.201004658  0.58
2010 Hartmann E, Oestreich M. Der asymmetrische konjugierte Silyltransfer in iterativen katalytischen Sequenzen: Synthese des C7-C16-Fragments von (+)-Neopeltolid Angewandte Chemie. 122: 6331-6334. DOI: 10.1002/Ange.201002916  0.582
2010 Schiffner J, Müther K, Oestreich M. Enantioselektive konjugierte Borylierung Angewandte Chemie. 122: 1214-1216. DOI: 10.1002/Ange.200906521  0.777
2010 Schiffner J, Müther K, Oestreich M. Enantioselektive konjugierte Borylierung Angewandte Chemie. 122: 1214-1216. DOI: 10.1002/Ange.200906521  0.777
2010 Weickgenannt A, Mewald M, Muesmann T, Oestreich M. Katalytische asymmetrische Si-O-Kupplung einfacher achiraler Silane und chiraler donorfunktionalisierter Alkohole Angewandte Chemie. 122: 2269-2272. DOI: 10.1002/Ange.200905561  0.786
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  0.614
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  0.783
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  0.689
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  0.676
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  0.803
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  0.8
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  0.83
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  0.631
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  0.457
2009 Schmidtmann ES, Oestreich M. ChemInform Abstract: Enantiospecific Synthesis and Allylation of All-Carbon-Substituted α-Chiral Allylic Stannanes. Cheminform. 40. DOI: 10.1002/chin.200942016  0.658
2009 Klare H, Bergander K, Oestreich M. Ein gezähmtes Silyliumion für Diels-Alder-Reaktionen bei niedrigen Temperaturen Angewandte Chemie. 121: 9241-9243. DOI: 10.1002/Ange.200904520  0.64
2009 Schmidtmann E, Oestreich M. Enantiospezifische Synthese und Allylierung ausschließlich Kohlenstoff-substituierter, α-chiraler Allylstannane Angewandte Chemie. 121: 4705-4709. DOI: 10.1002/Ange.200901384  0.655
2009 Klare H, Oestreich M. Asymmetrische Ringschlussmetathese mit Pfiff Angewandte Chemie. 121: 2119-2123. DOI: 10.1002/Ange.200806254  0.618
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  0.806
2009 Machotta AB, Oestreich M. Formation of Carbocycles The Mizoroki-Heck Reaction. 179-213. DOI: 10.1002/9780470716076.ch5  0.654
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  0.811
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  0.756
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  0.598
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  0.801
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  0.721
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  0.572
2008 Schiffner JA, Machotta AB, Oestreich M. A catalytic asymmetric Fujiwara-Moritani cyclization Synlett. 2271-2274. DOI: 10.1055/S-2008-1078271  0.818
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  0.783
2008 Rendler S, Oestreich M. Schlüssiger Nachweis eines SN2-Si-Mechanismus in der B(C6F5)3- katalysierten Hydrosilylierung von Carbonylverbindungen: Einsichten in die verwandte Hydrierung Angewandte Chemie. 120: 6086-6089. DOI: 10.1002/Ange.200801675  0.739
2008 Walter C, Oestreich M. Katalytische asymmetrische C-Si-Bindungsknüpfung an acyclischen α,β-ungesättigten Akzeptoren durch RhI-katalysierten konjugierten Silyltransfer mithilfe einer Si-B-Bindung Angewandte Chemie. 120: 3878-3880. DOI: 10.1002/Ange.200800361  0.552
2008 Rendler S, Oestreich M. Kinetische Racematspaltung und Desymmetrisierung durch stereoselektive Silylierung von Alkoholen Angewandte Chemie. 120: 254-257. DOI: 10.1002/Ange.200704210  0.716
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  0.688
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  0.629
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  0.731
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  0.776
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  0.786
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  0.773
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  0.775
2007 Oestreich M. Silicon-stereogenic silanes in asymmetric catalysis Synlett. 1629-1643. DOI: 10.1055/S-2007-980385  0.398
2007 Zimmermann A, Oestreich M. Asymmetric Synthesis - The Essentials Synthesis. 2007: 957-957. DOI: 10.1055/S-2007-973641  0.352
2007 Lloyd-Jones G, Rendler S, Oestreich M, Butts C. Intermolecular Chirality Transfer from Silicon to Carbon Synfacts. 2007: 0409-0409. DOI: 10.1055/S-2007-968362  0.74
2007 Trepohl VT, Oestreich M. Rhodium(I)-Catalyzed Conjugate Phosphination of Cyclic α,β-Unsaturated Ketones with Silylphosphines as Masked Phosphinides. Cheminform. 38. DOI: 10.1002/chin.200750186  0.788
2007 Rendler S, Oestreich M. Polishing a Diamond in the Rough: “Cu—H” Catalysis with Silanes Cheminform. 38. DOI: 10.1002/chin.200715247  0.695
2007 Klare H, Oestreich M. Chirale Erkennung mit siliciumstereogenen Silanen: außergewöhnliche Selektivitätsfaktoren bei der kinetischen Racematspaltung von donorfunktionalisierten Alkoholen Angewandte Chemie. 119: 9496-9499. DOI: 10.1002/Ange.200703847  0.627
2007 Rendler S, Oestreich M. Vom Schleifen eines “Rohdiamanten”: die “Cu-H”-Katalyse mit Silanen Angewandte Chemie. 119: 504-510. DOI: 10.1002/Ange.200602668  0.735
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  0.686
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  0.729
2006 Auer G, Oestreich M. Silylzincation of carbon-carbon multiple bonds revisited. Chemical Communications (Cambridge, England). 311-3. PMID 16391744 DOI: 10.1039/B513528A  0.604
2006 Oestreich M, Walter C, Auer G. Rh-Catalyzed Enantioselective 1,4-Addition of Silyl Boronic Esters Synfacts. 2006: 1142-1142. DOI: 10.1055/S-2006-949435  0.748
2006 Oestreich M, Walter C, Auer G. Rh-Catalyzed Enantioselective 1,4-Addition of Silyl Boronic Esters Synfacts. 2006: 1142-1142. DOI: 10.1055/s-2006-949435  0.345
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  0.824
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  0.799
2006 Machotta AB, Oestreich M. Organic Chemistry Online … and for Free? Angewandte Chemie International Edition. 45: 7114-7114. DOI: 10.1002/Anie.200603935  0.654
2006 Machotta AB, Oestreich M. Organische Chemie online… und gratis? Angewandte Chemie. 118: 7272-7272. DOI: 10.1002/Ange.200603935  0.675
2006 Walter C, Auer G, Oestreich M. Rhodiumkatalysierter enantioselektiver konjugierter Silyltransfer: 1,4-Addition von Silylboronsäureestern an cyclische Enone und Lactone Angewandte Chemie. 118: 5803-5805. DOI: 10.1002/Ange.200601747  0.715
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  0.823
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  0.794
2005 Oestreich M. Chirality transfer from silicon to carbon. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 30-7. PMID 16216041 DOI: 10.1002/Chem.200500782  0.421
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  0.761
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  0.78
2005 Oestreich M, Rendler S. ‘True’ Chirality Transfer from Silicon to Carbon Synfacts. 2005: 39-39. DOI: 10.1055/S-2005-869915  0.304
2005 Oestreich M. Neighbouring-group effects in Heck reactions European Journal of Organic Chemistry. 783-792. DOI: 10.1002/Ejoc.200400711  0.42
2005 Rendler S, Auer G, Oestreich M. Kinetische Racematspaltung von chiralen sekundären Alkoholen durch dehydrierende Kupplung mit zurückgewinnbaren, siliciumstereogenen Silanen Angewandte Chemie. 117: 7793-7797. DOI: 10.1002/Ange.200502631  0.755
2005 Rendler S, Auer G, Oestreich M. Kinetische Racematspaltung von chiralen sekundären Alkoholen durch dehydrierende Kupplung mit zurückgewinnbaren, siliciumstereogenen Silanen Angewandte Chemie. 117: 7793-7797. DOI: 10.1002/Ange.200502631  0.755
2005 Oestreich M, Rendler S. ?Echter? Chiralit�tstransfer von Silicium auf Kohlenstoff: asymmetrische Verst�rkung in einer reagenskontrollierten palladiumkatalysierten Hydrosilylierung Angewandte Chemie. 117: 1688-1691. DOI: 10.1002/Ange.200462355  0.713
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  0.655
2005 Brückner R, Würthner F, Tschierske C, Krüger A, Herges R, Ditrich K, Pfau R, Priepke H, Beifuss U, Bräse S, Marx A, Kirschning A, Sewald N, Senge MO, Müller TJJ, ... ... Oestreich M, et al. Organic chemistry 2004 | Organische chemie 2004 Nachrichten Aus Der Chemie. 53: 251-272.  0.31
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  0.808
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  0.788
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  0.737
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  0.632
2004 Oestreich M, Sempere-Culler F, Machotta AB. Katalytische desymmetrisierende intramolekulare Heck-Reaktion: Nachweis einer ungewöhnlichen hydroxydirigierten Alkeninsertion Angewandte Chemie. 117: 152-155. DOI: 10.1002/Ange.200460921  0.804
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  0.768
2003 Oestreich M, Schmid UK, Auer G, Keller M. A Convergent Method for the Synthesis of Highly Enantiomerically Enriched Cyclic Silanes with Silicon-Centered Chirality Synthesis. 2003: 2725-2739. DOI: 10.1055/S-2003-42477  0.633
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  0.737
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  0.673
2001 Oestreich M, Dennison PR, Kodanko JJ, Overman LE. Vereitelteβ-Hydrideliminierung: Abfangen der Alkylpalladiumzwischenstufe einer asymmetrischen intramolekularen Heck-Reaktion Angewandte Chemie. 113: 1485-1489. DOI: 10.1002/1521-3757(20010417)113:8<1485::Aid-Ange1485>3.0.Co;2-F  0.71
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  0.459
1999 Oestreich M, Fröhlich R, Hoppe D. (−)-Sparteine-Mediated Stereoselective Intramolecular Carbolithiation of 4-Substituted 5-Hexynyl Carbamates. Synthesis of Enantiopure 1,3-Difunctionalized Alkylidene Cyclopentanes The Journal of Organic Chemistry. 64: 8616-8626. DOI: 10.1021/Jo991095U  0.415
1999 Oestreich M, Hoppe D. (−)-Sparteine-mediated stereoselective intramolecular conjugate addition reactions of dienes and enynes Tetrahedron Letters. 40: 1881-1884. DOI: 10.1016/S0040-4039(99)00092-1  0.515
1999 Hoppe D, Woltering M, Oestreich M, Fröhlich R. (−)-Sparteine-Mediated Asymmetric Intramolecular Carbolithiation of Alkenes: Synthesis of Enantiopure Cyclopentanes with Three Consecutive Stereogenic Centers Helvetica Chimica Acta. 82: 1860-1877. DOI: 10.1002/(Sici)1522-2675(19991110)82:11<1860::Aid-Hlca1860>3.0.Co;2-8  0.612
1998 Oestreich M, Fröhlich R, Hoppe D. (−)-Sparteine-mediated stereoselective intramolecular carbolithiation of alkynes Tetrahedron Letters. 39: 1745-1748. DOI: 10.1016/S0040-4039(98)00085-9  0.439
1998 Oestreich M, Fröhlich R, Hoppe D. (−)-Sparteine-mediated stereoselective intramolecular carbolithiation of alkynes Tetrahedron Letters. 39: 1745-1748. DOI: 10.1016/S0040-4039(98)00085-9  0.439
1997 Micouin L, Oestreich M, Knochel P. Stereoselective Preparation and Reactions of Cycloalkylzinc Compounds Angewandte Chemie International Edition in English. 36: 245-246. DOI: 10.1002/Anie.199702451  0.419
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