作者:Meng-Yang Chang、Si-Yun Wang、Chun-Li Pai
DOI:10.1016/j.tetlet.2006.06.156
日期:2006.9
Substituted 4,4-diaryl-3-butenyl-l-amines are synthesized in nearly 34-47% overall yields starting from 3-hydroxypiperidine by the regioselective Baeyer-Villiger lactonization, Grignard addition and elimination sequence. This facile strategy was also used to synthesize racemic SKF 89976A. (c) 2006 Elsevier Ltd. All rights reserved.