Cobalt-catalyzed cyclization with the introduction of cyano, acyl and aminoalkyl groups

被引:8
|
作者
Hori, Hiroto [1 ]
Arai, Shigeru [1 ,2 ]
Nishida, Atsushi [1 ,2 ]
机构
[1] Chiba Univ, Grad Sch Pharmaceut Sci, Chuo Ku, 1-8-1 Inohana, Chiba 2608675, Japan
[2] Chiba Univ, Mol Chiral Res Ctr, Inage Ku, 1-33 Yayoi Cho, Chiba 2638522, Japan
基金
日本学术振兴会;
关键词
STEREOSELECTIVE HYDROCYANATION; ACYLPHOSPHONATE DERIVATIVES; RADICAL CYCLIZATIONS; PHOSPHONATE GROUP; TERMINAL ALKYNES; BETA-ELIMINATION; OLEFINS; MARKOVNIKOV; ALLENES; ALKENES;
D O I
10.1039/c9ob00637k
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An efficient synthesis of carbo-and heterocycles using CvC, CvO and CvN bonds under cobalt catalysis is described. The substituents on olefins are key for controlling the regio-and chemoselectivity in the initial hydrogen atom transfer step and quaternary carbons are efficiently constructed under mild conditions. Cyclopropane cleavage and tandem cyclization give highly functionalized bicyclic skeletons in a single operation.
引用
收藏
页码:4783 / 4788
页数:6
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