SYNTHESIS OF AN 11-DEOXY-8-AZAPROSTAGLANDIN-E1 INTERMEDIATE

被引：25

作者：

BARCO, A

BENETTI, S

POLLINI, GP

BARALDI, PG

SIMONI, D

VICENTINI, CB

机构：

[1] IST CHIM,I-44100 FERRARA,ITALY

[2] IST CHIM FARMACEUT,I-44100 FERRARA,ITALY

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1979年 / 44卷 / 10期

关键词：

D O I：

10.1021/jo01324a041

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

In recent years considerable chemical and medicinal interest has been focused on prostaglandin analogues in which carbon atoms are replaced by heteroatoms.1 Among the azaprostaglandin analogues, which contain one or more nitrogens at almost every position of the cyclopentane nucleus, the 11-deoxy-8-azaprostaglandin E1 (1) is of special interest because of the attract ive biological activities. © 1979, American Chemical Society. All rights reserved.

引用

页码：1734 / 1736

页数：3

共 13 条

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