Direct synthesis of α-ketothioamides from aryl methyl ketones and amines via I 2-promoted sp 3 C–H functionalization
HZ Li, WJ Xue, AX Wu
Index: Li, Hong-Zheng; Xue, Wei-Jian; Wu, An-Xin Tetrahedron, 2014 , vol. 70, # 31 p. 4645 - 4651
Full Text: HTML
Citation Number: 5
Abstract
As an important transformation in synthetic chemistry, C–H bond functionalization has been extensively pursued and widely examined by organic chemists. 1 In recent years, numerous methods have been established for the conversion of a C–H bond to a C–Z bond (such as C–C, C–N, and
Related Articles:
A selective reductive amination of aldehydes by the use of Hantzsch dihydropyridines as reductant
[Itoh, Takashi; Nagata, Kazuhiro; Miyazaki, Michiko; Ishikawa, Hiroyuki; Kurihara, Ayako; Ohsawa, Akio Tetrahedron, 2004 , vol. 60, # 31 p. 6649 - 6655]
[Itoh, Takashi; Nagata, Kazuhiro; Kurihara, Ayako; Miyazaki, Michiko; Ohsawa, Akio Tetrahedron Letters, 2002 , vol. 43, # 17 p. 3105 - 3108]