A NEW STRATEGY FOR THE ENANTIOSELECTIVE SYNTHESIS OF ASPIDOSPERMA ALKALOIDS .2. ACHIEVEMENT OF THE PENTACYCLIC SYSTEM

被引：28

作者：

DESMAELE, D

DANGELO, J

机构：

[1] Unité de Chimie Organique Associée au CNRS, ESPCI, 75231 Paris Cedex 05

来源：

TETRAHEDRON LETTERS | 1990年 / 31卷 / 06期

关键词：

D O I：

10.1016/S0040-4039(00)94654-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Carbazolone 5 has been converted in eleven steps into alkaloid analog 1 (R = Me) (13% overall yield). © 1990.

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页码：883 / 886

页数：4

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[1] A NEW STRATEGY FOR THE ENANTIOSELECTIVE SYNTHESIS OF ASPIDOSPERMA ALKALOIDS .1. CONSTRUCTION OF THE [ABC]-TYPE TRICYCLIC INTERMEDIATES
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[J]. TETRAHEDRON LETTERS, 1990, 31 (06) : 879 - 882
[2] PENTACYCLIC SYSTEMS FOR INDOLE ALKALOIDS - FORMATION OF THE C-11-C-12 BOND - 2 SYNTHESES OF (/-)-ASPIDOSPERMIDINE
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