A NEW ACCESS TO HOMOERYTHRINA ALKALOIDS

被引:43
作者
LEDREAU, MA [1 ]
DESMAELE, D [1 ]
DUMAS, F [1 ]
DANGELO, J [1 ]
机构
[1] FAC PHARM CHATENAY MALABRY,CNRS,CHIM ORGAN LAB,5 RUE J B CLEMENT,F-92296 CHATENAY MALABRY,FRANCE
关键词
D O I
10.1021/jo00063a004
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A new spiroannulation reaction based on a “one-pot”, tandem alkylation-Michael addition sequence of 2-tetralone has been developed. The combination of this process with an intramolecular Schmidt rearrangement of an azido ketone allows an efficient access to the Homoerythrina skeleton. © 1993, American Chemical Society. All rights reserved.
引用
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页码:2933 / 2935
页数:3
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