| Year |
Citation |
Score |
| 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 |
0.6 |
|
| 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 |
0.64 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
0.8 |
|
| 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 |
1 |
|
| 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 |
0.36 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
1 |
|
| 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 |
0.72 |
|
| 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 |
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 |
0.01 |
|
| 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 |
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 |
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 |
0.72 |
|
| 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 |
1 |
|
| 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 |
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 |
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 CH 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 CN 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 2013 |
Müther K, Mohr J, Oestreich M. Silylium ion promoted reduction of imines with hydrosilanes Organometallics. 32: 6643-6646. DOI: 10.1021/om4002796 |
1 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 2011 |
Königs CDF, Oestreich M. Shortened synthesis of a silicon-stereogenic cyclic silane Synthesis. 2062-2065. DOI: 10.1055/s-0030-1259989 |
1 |
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| 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 |
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| 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 |
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| 2011 |
Hartmann E, Oestreich M. Si-B bond activation in asymmetric Cu(I) and Rh(I) catalysis Chimica Oggi. 29: 34-36. |
1 |
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| 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 |
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| 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 |
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| 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 |
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| 2010 |
Klare HF, Oestreich M. Silylium ions in catalysis. Dalton Transactions (Cambridge, England : 2003). 39: 9176-84. PMID 20405073 DOI: 10.1039/c003097j |
1 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 2009 |
Machotta AB, Oestreich M. Formation of Carbocycles The Mizoroki-Heck Reaction. 179-213. DOI: 10.1002/9780470716076.ch5 |
1 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 2008 |
Schiffner JA, Machotta AB, Oestreich M. A catalytic asymmetric Fujiwara-Moritani cyclization Synlett. 2271-2274. DOI: 10.1055/s-2008-1078271 |
1 |
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| 2008 |
Oestreich M. Directed Mizoroki-Heck reactions Topics in Organometallic Chemistry. 24: 169-192. DOI: 10.1007/3418_2007_063 |
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| 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 |
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| 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 |
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| 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. |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 2007 |
Oestreich M. Silicon-stereogenic silanes in asymmetric catalysis Synlett. 1629-1643. DOI: 10.1055/s-2007-980385 |
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| 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. |
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| 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 |
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| 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 |
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| 2006 |
Auer G, Oestreich M. Silylzincation of carbon-carbon multiple bonds revisited. Chemical Communications (Cambridge, England). 311-3. PMID 16391744 DOI: 10.1039/b513528a |
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| 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 |
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| 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 |
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| 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 |
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| 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. |
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| 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 |
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| 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 |
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| 2005 |
Oestreich M. Strategies for catalytic asymmetric electrophilic alpha halogenation of carbonyl compounds. Angewandte Chemie (International Ed. in English). 44: 2324-7. PMID 15827954 DOI: 10.1002/anie.200500478 |
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| 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 |
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| 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 |
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| 2005 |
Oestreich M. Neighbouring-group effects in Heck reactions European Journal of Organic Chemistry. 783-792. DOI: 10.1002/ejoc.200400711 |
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| 2005 |
Oestreich M. Kaleidoscope of catalysis: Heidelberg Forum of Molecular Catalysis 2005 Angewandte Chemie - International Edition. 44: 5166-5167. DOI: 10.1002/anie.200502426 |
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| 2005 |
Oestreich M. Swiss delight: Bürgenstock 2005 Angewandte Chemie - International Edition. 44: 3512-3513. DOI: 10.1002/anie.200501433 |
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| 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 |
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| 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. |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 2004 |
Oestreich M. Ways to (-)-galanthamine | Wege zu (-)-Galanthamin Nachrichten Aus Der Chemie. 52: 688-691. |
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| 2004 |
Oestreich M. A new iron in the fire | Ein neues eisen im feuer Nachrichten Aus Der Chemie. 52: 446-449. |
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| 2004 |
Würthner F, Krüger A, Herges R, Ditrich K, Priepke H, Pfau R, Bräse S, Kirschning A, Sewald N, Senge MO, Müller TJJ, Bach T, Heydt H, Hartung J, Schreiner PR, ... ... Oestreich M, et al. Organic chemistry 2003 | Organische chemie 2003 Nachrichten Aus Der Chemie. 52: 267-291. |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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