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

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1993年 / 58卷 / 11期

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

页码：2933 / 2935

页数：3

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