作者: Reymundo A. Villa , Qihai Xu , Ohyun Kwon
DOI: 10.1021/OL302077N
关键词:
摘要: The total synthesis of the indole alkaloid hirsutine has been achieved, with a key step being application our phosphine-catalyzed [4 + 2] annulation an imine ethyl α-methylallenoate. From commercially available indole-2-carboxaldehyde, target was synthesized in 14 steps and 6.7% overall yield.