A STRAIGHTFORWARD ROUTE TO IBOPHYLLIDINE ALKALOIDS BY A DOUBLE TRANSANNULAR CYCLIZATION

被引：17

作者：

FERNANDEZ, JC ^{[1
]}

VALLS, N ^{[1
]}

BOSCH, J ^{[1
]}

BONJOCH, J ^{[1
]}

机构：

[1] UNIV BARCELONA,FAC PHARM,ORGAN CHEM LAB,E-08028 BARCELONA,SPAIN

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1995年 / 22期

关键词：

D O I：

10.1039/C39950002317

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Ring cleavage of indolo[2,3-a]quinolizidine 4 to an octahydroazecino[5,4-b]indole system, followed by introduction of a cyano substituent and double transannular cyclization gives (+/-)-deethylibophyllidine.

引用

页码：2317 / 2318

页数：2

共 21 条

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