Substituted 4,4-diaryl-3-butenyl-1-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
Chang, Meng-Yang,Wang, Si-Yun,Pai, Chun-Li
p. 6389 - 6392
(2007/10/03)
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