IMINOPHOSPHORANE-MEDIATED SYNTHESIS OF 1-SUBSTITUTED-BETA-CARBOLINES - INVESTIGATIVE STUDIES ON THE PREPARATION OF ALKALOIDS LAVENDAMYCIN AND EUDISTOMINS FRAMEWORK

被引：16

作者：

MOLINA, P

FRESNEDA, PM

CANOVAS, M

机构：

[1] Departamento de Química Orgánica, Facultad de Química, Universidad de Murcia, E-30071 Murcia, Campus de Espinardo

来源：

TETRAHEDRON LETTERS | 1992年 / 33卷 / 20期

关键词：

D O I：

10.1016/S0040-4039(00)78888-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Aza-Wittig reaction of iminophosphorane 3, derived from ethyl alpha-azido-beta-(3-indolyl) propenoate and triphenylphosphine, with 2-formylpyrrole and 2-formylquinolines leads to Eudistomins A and M and Lavendamycin derivatives respectively.

引用

页码：2891 / 2894

页数：4

共 17 条

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