Prof. Dr. Martin Oestreich - Publications

2420 Single-Electron Transfer Reactions in Frustrated and Conventional Silylium Ion/Phosphane Lewis Pairs A. Merk, H. Großekappenberg, M. Schmidtmann, M. P. Luecke, C. Lorent, M. Driess, M. Oestreich, H. F. T. Klare, T. Müller Angewandte Chemie International Edition 2018, 57, 15267–15271, 10.1002/anie.201808922

2388 Transfer Hydrocyanation of α- and α,β-Substituted Styrenes Catalyzed by Boron Lewis Acids P. Orecchia, W. Yuan, M. Oestreich Angewandte Chemie International Edition 2019, 58, 3579–3583, 10.1002/anie.201813853

2387 Palladium‐Catalyzed Three‐Component Reaction of Dihydrosilanes and Vinyl Iodides in the Presence of Alcohols: Rapid Assembly of Silyl Ethers of Tertiary Silanes W. Yuan, P. Orecchia, M. Oestreich Chemistry – A European Journal 2018, 24, 19175–19178, 10.1002/chem.201805595

2330 Z-Selective Hydrostannylation of Terminal and Internal C–C Triple Bonds Initiated by the Trityl Cation F. Forster, V. M. Rendón López, M. Oestreich Organometallics 2018, 37, 2656–2659, 10.1021/acs.organomet.8b00409

2307 Custom Hydrosilane Synthesis Based on Monosilane W. Yuan, P. Smirnov, M. Oestreich Chem 2018, 4, 1443–1450, 10.1016/j.chempr.2018.03.017

2203 Bis(silylenyl)-substituted ferrocene-stabilized η6-arene iron(0) complexes: synthesis, structure and catalytic application M. P. Luecke, D. Porwal, A. Kostenko, Y. P. Zhou, S. Yao, M. Keck, C. Limberg, M. Oestreich, M. Driess Dalton Transactions 2017, 46, 16412–16418, 10.1039/C7DT03301J

2155 Cooperative Al–H Bond Activation in DIBAL-H: Catalytic Generation of an Alumenium-Ion-Like Lewis Acid for Hydrodefluorinative Friedel–Crafts Alkylation F. Forster, T. T. Metsänen, E. Irran, P. Hrobárik, M. Oestreich Journal of the American Chemical Society 2017, 139, 16334–16342, 10.1021/jacs.7b09444

2154 Two-Silicon Cycle for Carbonyl Hydrosilylation with Nikonov’s Cationic Ruthenium(II) Catalyst J. Fuchs, H. F. T. Klare, M. Oestreich ACS Catalysis 2017, 7, 8338–8342, 10.1021/acscatal.7b03336

2153 Cyclohexa-1,3-diene-based dihydrogen and hydrosilane surrogates in B(C6F5)3-catalysed transfer processes W. Yuan, P. Orecchia, M. Oestreich Chemical Communications 2017, 53, 10390–10393, 10.1039/c7cc06195a

2152 B(C6F5)3-Catalyzed Reduction of Sulfoxides and Sulfones to Sulfides with Hydrosilanes D. Porwal, M. Oestreich Synthesis 2017, 49, 4698–4702, 10.1055/s-0036-1588476

2151 BArF3-Catalyzed Imine Hydroboration with Pinacolborane Not Requiring the Assistance of an Additional Lewis Base Q. Yin, Y. Soltani, R. L. Melen, M. Oestreich Organometallics 2017, 36, 2381–2384, 10.1021/acs.organomet.7b00381

2150 B(C6F5)3-katalysierte chemoselektive Defunktionalisierung von etherhaltigen primären Alkyltosylaten mit Hydrosilanen I. Chatterjee, D. Porwal, M. Oestreich Angewandte Chemie 2017, 129, 3438–3441, 10.1002/ange.201611813

2149 B(C6F5)3-Catalyzed Chemoselective Defunctionalization of Ether-Containing Primary Alkyl Tosylates with Hydrosilanes I. Chatterjee, D. Porwal, M. Oestreich Angewandte Chemie International Edition 2017, 56, 3389–3391, 10.1002/anie.201611813

1973 B(C6F5)3-Catalyzed Reduction of Aromatic and Aliphatic Nitro Groups with Hydrosilanes D. Porwal, M. Oestreich European Journal of Organic Chemistry 2016, 2016, 3307–3309, 10.1002/ejoc.201600556

1972 Brønsted Acid-Catalyzed Transfer Hydrogenation of Imines and Alkenes Using Cyclohexa-1,4-dienes as Dihydrogen Surrogates I. Chatterjee, M. Oestreich Organic Letters 2016, 18, 2463–2466, 10.1021/acs.orglett.6b01016

1971 Metal-Free Phosphine Oxide Reductions Catalyzed by B(C6F5)3 and Electrophilic Fluorophosphonium Cations M. Mehta, I. Garcia de la Arada, M. Perez, D. Porwal, M. Oestreich, D. W. Stephan Organometallics 2016, 35, 1030–1035, 10.1021/acs.organomet.6b00158

1713 Extending the Scope of the B(C6F5)3-Catalyzed C=N Bond Reduction: Hydrogenation of Oxime Ethers and Hydrazones J. Mohr, D. Porwal, I. Chatterjee, M. Oestreich Chemistry - A European Journal 2015, 21, 17583–17586, 10.1002/chem.201503509

1712 B(C6F5)3-Catalyzed Transfer of Dihydrogen from One Unsaturated Hydrocarbon to Another I. Chatterjee, Z. W. Qu, S. Grimme, M. Oestreich Angewandte Chemie International Edition 2015, 54, 12158–12162, 10.1002/anie.201504941

1711 Peripheral mechanism of a carbonyl hydrosilylation catalysed by an SiNSi iron pincer complex T. T. Metsänen, D. Gallego, T. Szilvási, M. Driess, M. Oestreich Chem. Sci. 2015, 6, 7143–7149, 10.1039/C5SC02855H

1710 Mechanism of the cooperative Si–H bond activation at Ru–S bonds T. Stahl, P. Hrobárik, C. D. F. Königs, Y. Ohki, K. Tatsumi, S. Kemper, M. Kaupp, H. F. T. Klare, M. Oestreich Chem. Sci. 2015, 6, 4324–4334, 10.1039/C5SC01035G

1465 Temperature-Dependent Chemoselective Hydrosilylation of Carbon Dioxide to Formaldehyde or Methanol Oxidation State T. T. Metsänen, M. Oestreich Organometallics 2015, 34, 543–546, 10.1021/om501279a

1464 B(C6F5)3-Catalyzed Transfer Hydrogenation of Imines and Related Heteroarenes Using Cyclohexa-1,4-dienes as a Dihydrogen Source I. Chatterjee, M. Oestreich Angewandte Chemie International Edition 2015, 54, 1965–1968, 10.1002/anie.201409246

1463 Chemoselective Tin–Boron Exchange Aided by the Use of Dummy Ligands at the Tin Atom J. Hermeke, M. Mewald, E. Irran, M. Oestreich Organometallics 2014, 33, 5097–5100, 10.1021/om500851r

1404 Direct Catalytic Access to N-Silylated Enamines from Enolizable Imines and Hydrosilanes by Base-Free Dehydrogenative Si–N Coupling J. Hermeke, H. F. T. Klare, M. Oestreich Chemistry - A European Journal 2014, 20, 9250–9254, 10.1002/chem.201402866

1403 Insight into the Mechanism of Carbonyl Hydrosilylation Catalyzed by Brookhart’s Cationic Iridium(III) Pincer Complex T. T. Metsänen, P. Hrobárik, H. F. T. Klare, M. Kaupp, M. Oestreich Journal of the American Chemical Society 2014, 136, 6912–6915, 10.1021/ja503254f

1176 Experimental Analysis of the Catalytic Cycle of the Borane-Promoted Imine Reduction with Hydrosilanes: Spectroscopic Detection of Unexpected Intermediates and a Refined Mechanism J. Hermeke, M. Mewald, M. Oestreich Journal of the American Chemical Society 2013, 135, 17537–17546, 10.1021/ja409344w

1175 The Family of Ferrocene-Stabilized Silylium Ions: Synthesis, 29Si NMR Characterization, Lewis Acidity, Substituent Scrambling, and Quantum-Chemical Analyses K. Müther, P. Hrobárik, V. Hrobáriková, M. Kaupp, M. Oestreich Chemistry - A European Journal 2013, 19, 16579–16594, 10.1002/chem.201302885