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.

引用

收藏

页码：883 / 886

页数：4

相关论文

共 5 条

[1] A NEW STRATEGY FOR THE ENANTIOSELECTIVE SYNTHESIS OF ASPIDOSPERMA ALKALOIDS .1. CONSTRUCTION OF THE [ABC]-TYPE TRICYCLIC INTERMEDIATES [J].

DANGELO, J ;

DESMAELE, D .

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 [J].

GALLAGHER, T ;

MAGNUS, P ;

HUFFMAN, JC .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1983, 105 (14) :4750-4757

[3] A NEW EFFICIENT ACCESS TO CYCLIC IMINES [J].

LAMBERT, PH ;

VAULTIER, M ;

CARRIE, R .

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1982, (21) :1224-1225

[4] 3-HYDROXYMETHYLINDOLES [J].

LEETE, E .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1959, 81 (22) :6023-6026

[5] On new organic phosphorus bonding III Phosphine methylene derivatives and phosphinimine [J].

Staudinger, H ;

Meyer, J .

HELVETICA CHIMICA ACTA, 1919, 2 :635-646