Effective Formylation of Amines with Carbon Dioxide and Diphenylsilane Catalyzed by Chelating bis(tzNHC) Rhodium Complexes

被引:153
作者
Nguyen, Thanh V. Q. [1 ]
Yoo, Woo-Jin [1 ]
Kobayashi, Shu [1 ]
机构
[1] Univ Tokyo, Sch Sci, Dept Chem, Tokyo, Japan
基金
日本科学技术振兴机构; 日本学术振兴会;
关键词
amides; carbon dioxide; formylation; N-heterocylic carbenes; rhodium; N-HETEROCYCLIC CARBENES; DIPHOSPHINE COMPLEX; FORMIC-ACID; ATM; CO2; REDUCTION; HYDROSILYLATION; TRANSFORMATION; METHYLATION; METHANOL;
D O I
10.1002/anie.201504072
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reductive formylation of amines using CO2 and hydrosilanes is an attractive method for incorporating CO2 into valuable organic compounds. However, previous systems required either high catalyst loadings or high temperatures to achieve high efficiency, and the substrate scope was mostly limited to simple amines. To address these problems, a series of alkyl bridged chelating bis(NHC) rhodium complexes (NHC=N-heterocyclic carbene) have been synthesized and applied to the reductive formylation of amines using CO2 and Ph2SiH2. A rhodium-based bis(tzNHC) complex (tz=1,2,3-triazol-5-ylidene) was identified to be highly effective at a low catalyst loading and ambient temperature, and a wide substrate scope, including amines with reducible functional groups, were compatible.
引用
收藏
页码:9209 / 9212
页数:4
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