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Angewandte Chemie (International Ed. in English)|January 30, 2016
Friedel-Crafts-Type Intermolecular C-H Silylation of Electron-Rich Arenes Initiated by Base-Metal SaltsQin Yin, Hendrik F T Klare, Martin Oestreich
Zeitschrift Fur Kardiologie|January 1, 1989
[Suppression of coronary sclerosis in hypertensive rats by calcium channel antagonists without lowering blood pressure]P E Schwabedal, W Oestreich, S C Szathmary
Journal of the American Chemical Society|January 18, 2018
Catalytic Dehydrogenative Stannylation of C(sp)-H Bonds Involving Cooperative Sn-H Bond Activation of HydrostannanesFrancis Forster, Victoria M Rendón López, Martin Oestreich
Organic Letters|December 2, 2017
Copper-Catalyzed Substitution of α-Triflyloxy Nitriles and Esters with Silicon Nucleophiles under Inversion of the ConfigurationJonas Scharfbier, Hamideh Hazrati, Elisabeth Irran, et al.
The Journal of Organic Chemistry|March 7, 2023
Intramolecular 7-<i>endo</i>-<i>dig</i>-Selective Carbosilylation of Internal Alkynes Involving Silylium-Ion RegenerationHonghua Zuo, Hendrik F T Klare, Martin Oestreich
Journal of the American Chemical Society|February 1, 2023
Catalytically Generated Meerwein's Salt-Type Oxonium Ions for Friedel-Crafts C(sp<sup>2</sup>)-H Methylation with MethanolTao He, Hendrik F T Klare, Martin Oestreich
Chemistry (Weinheim an Der Bergstrasse, Germany)|October 23, 2015
Extending the Scope of the B(C6 F5 )3 -Catalyzed C=N Bond Reduction: Hydrogenation of Oxime Ethers and HydrazonesJens Mohr, Digvijay Porwal, Indranil Chatterjee, et al.
Angewandte Chemie (International Ed. in English)|February 19, 2021
Consecutive β,β'-Selective C(sp<sup>3</sup> )-H Silylation of Tertiary Amines with Dihydrosilanes Catalyzed by B(C<sub>6</sub> F<sub>5</sub> )<sub>3</sub>Huaquan Fang, Kaixue Xie, Sebastian Kemper, et al.
Angewandte Chemie (International Ed. in English)|May 30, 2019
Copper-Catalyzed Regio- and Enantioselective Addition of Silicon Grignard Reagents to Alkenes Activated by Azaaryl GroupsWenbin Mao, Weichao Xue, Elisabeth Irran, et al.
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