An expeditious route to carbocyclic nucleosides: (-)-aristeromycin and (-)-carbodine

被引：33

作者：

Burlina, F

Favre, A

Fourrey, JL

Thomas, M

机构：

[1] CNRS,INST CHIM SUBST NAT,F-91198 GIF SUR YVETTE,FRANCE

[2] CNRS,INST JACQUES MONOD,F-75251 PARIS 05,FRANCE

来源：

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS | 1997年 / 7卷 / 03期

关键词：

D O I：

10.1016/S0960-894X(96)00619-1

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

The readily available bicyclic lactone (-)-1 was transformed into diacetate (-)-2 which served in an expeditious route to (-)-aristeromycin (3a) and (-)-carbodine (3b) in acceptable yields. (C) 1997, Elsevier Science Ltd.

引用

页码：247 / 250

页数：4

共 31 条

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