Exploring new uses for C-H amination: Ni-catalyzed cross-coupling of cyclic sulfamates

被引:78
作者
Wehn, PM [1 ]
Du Bois, J [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
D O I
10.1021/ol051896l
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Benzene-fused cyclic sulfamates are prepared from ortho-substituted phenolic starting materials through selective C-H amination or olefin aziridination. These unique heterocycles will engage in Ni-catalyzed cross-coupling reactions with aryl- and alkyl-Grignard reagents. Application of modern tools for C-N and C-C bond formation thus makes readily available functional amine derivatives and augments the possible uses for C-H amination in synthesis.
引用
收藏
页码:4685 / 4688
页数:4
相关论文
共 23 条
[21]   MECHANISM OF BIARYL SYNTHESIS WITH NICKEL-COMPLEXES [J].
TSOU, TT ;
KOCHI, JK .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1979, 101 (25) :7547-7560
[22]   Stereochemical models for Rh-catalyzed amination reactions of chiral sulfamates [J].
Wehn, PM ;
Lee, JH ;
Du Bois, J .
ORGANIC LETTERS, 2003, 5 (25) :4823-4826
[23]  
WEHN PM, UNPUB