A short route for the construction of the tetracyclic ring system of silicine-methuenine alkaloids

被引：20

作者：

Bennasar, ML

Vidal, B

Lazaro, A

Kumar, R

Bosch, J

机构：

[1] Laboratory of Organic Chemistry, Faculty of Pharmacy, University of Barcelona

来源：

TETRAHEDRON LETTERS | 1996年 / 37卷 / 20期

关键词：

D O I：

10.1016/0040-4039(96)00607-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A general synthetic entry to the tetracyclic ring system of silicine-methuenine alkaloids, involving the partial hydrogenation of dihydropyridines 2 followed by PPSE-induced cyclization of the resulting tetrahydropyridine esters 3, is reported. Copyright (C) 1996 Published by Elsevier Science Ltd

引用

页码：3541 / 3544

页数：4

共 7 条

[1] 1ST TOTAL SYNTHESIS OF THE INDOLE ALKALOID ERVITSINE - A STRAIGHTFORWARD, BIOMIMETIC APPROACH [J].