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Decarboxylative Cyclization of Allylic Cyclic Carbamates: Mechanism Studies and Applications to the Synthesis of Natural Products
作者姓名:Joseph  C.  Calabrese
作者单位:Du Pont
摘    要:The mechanism of decarboxylative cyclization of allylic cyclic carbamates 1 leading to 2-substituted △~3-piperidines and-pyrrolidines, as well as its applications to the total synthesis of (--)codonopsine, are described.


Decarboxylative Cyclization of Allylic Cyclic Carbamates: Mechanism Studies and Applications to the Synthesis of Natural Products
Joseph C. Calabrese.Decarboxylative Cyclization of Allylic Cyclic Carbamates: Mechanism Studies and Applications to the Synthesis of Natural Products[J].Chinese Journal of Organic Chemistry,1993(2).
Authors:WANG Chia-Lin J  Joseph C Calabrese Du Pont Merck Pharmaceutical Co  Experimental Station  P O Box  Wilmington  DE Du Pont Co  CR&DD  Experimental Station
Institution:WANG Chia-Lin J.,Joseph C. Calabrese Du Pont Merck Pharmaceutical Co.,Experimental Station,P. O. Box 80353,Wilmington,DE 19880 0353 Du Pont Co.,CR&DD,Experimental Station
Abstract:
Keywords:mechanism  allylic cyclic carbamates  codonopsine
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