New efficient method in nucleoside synthesis

被引：24

作者：

Jungmann, O ^{[1
]}

Pfleiderer, W ^{[1
]}

机构：

[1] UNIV KONSTANZ,FAK CHEM,D-78434 CONSTANCE,GERMANY

来源：

TETRAHEDRON LETTERS | 1996年 / 37卷 / 46期

关键词：

D O I：

10.1016/0040-4039(96)01929-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A new stereo- and regioselective synthesis for adenosine analogous nucleosides is described. Starting from 2- and 6-substituted 4-amino-7(8H)-pteridinones, DBU deprotonation and the ribosylation with an alpha-haloribofuranose derivative leads to the corresponding pteridine-N-8-beta-D-nucleosides in reasonably good yields(1). Copyright (C) 1996 Published by Elsevier Science Ltd

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页码：8355 / 8358

页数：4

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