Bench-Stable Cobalt Pre-Catalysts for Mild Hydrosilative Reduction of Tertiary Amides to Amines and Beyond

被引:38
作者
Nurseiit, Alibek [1 ]
Janabel, Jaysan [1 ]
Gudun, Kristina A. [1 ]
Kassymbek, Aishabibi [1 ]
Segizbayev, Medet [1 ]
Seilkhanov, Tulegen M. [2 ]
Khalimon, Andrey Y. [1 ]
机构
[1] Nazarbayev Univ, Dept Chem, Sch Sci & Technol, 53 Kabanbay Batyr Ave, Astana 010000, Kazakhstan
[2] Sh Ualikhanov Kokshetau State Univ, Lab Engn Profile NMR Spect, 76 Abay St, Kokshetau 020000, Kazakhstan
关键词
cobalt; hydrosilylation; amides; homogeneous catalysis; CHEMOSELECTIVE REDUCTION; ALKENE HYDROSILYLATION; HOMOGENEOUS CATALYSIS; CARBONYL-COMPOUNDS; ORGANIC-SYNTHESIS; SECONDARY AMIDES; MANGANESE; IRON; KETONES; ESTERS;
D O I
10.1002/cctc.201801605
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The readily synthesized and bench-stable cobalt dichloride complex (dpephos)CoCl2 is employed as a pre-catalyst for a diversity of silane additions to unsaturated organic molecules, including the normally challenging reduction of amides to amines. With regard to hydrosilative reduction of amides even more effective and activator free catalytic systems can be generated from the bench-stable, commercially available Co(acac)(2) and Co(OAc)(2) with dpephos and PPh3 ligands. These systems operate under mild conditions (<100 degrees C), with many examples of room temperature transformations, presenting a first example of mild cobalt-catalyzed hydrosilylation of amides.
引用
收藏
页码:790 / 798
页数:9
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