作者:Miwako Mori、Masaya Kimura、Yasuhiro Uozumi、Yoshio Ban
DOI:10.1016/s0040-4039(00)98268-6
日期:1985.1
A one step synthesis of 1,4-benzodiazepines from o-haloanilines and amino acids was achieved by use of palladium catalyzed carbonylation, by which application a synthesis of the model compounds(23a and 23b) of Neothramycin (A and B) was described. An efficient chemoselective reduction of the amide was provided.
通过钯催化的羰基化反应,由邻卤代苯胺和氨基酸一步合成1,4-苯并二氮杂pine,描述了新霉素(A和B)的模型化合物(23a和23b)的合成。提供了酰胺的有效化学选择性还原。