A CONVENIENT AND STEREOSELECTIVE SYNTHESIS OF 2'-DEOXY-BETA-L-RIBONUCLEOSIDES

被引：17

作者：

FUJIMORI, S

IWANAMI, N

HASHIMOTO, Y

SHUDO, K

机构：

[1] UNIV TOKYO,FAC PHARMACEUT SCI,BUNKYO KU,TOKYO 113,JAPAN

[2] UNIV TOKYO,INST APPL MICROBIOL,BUNKYO KU,TOKYO 113,JAPAN

来源：

NUCLEOSIDES & NUCLEOTIDES | 1992年 / 11卷 / 2-4期

关键词：

D O I：

10.1080/07328319208021708

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

2'-Deoxy-beta-L-ribonucleosides containing usual bases which are useful as synthons for modified oligodeoxyribonucleotides, were conveniently synthesized by a stereoselective glycosylation procedure. The method is suitable for large-scale preparations.

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页码：341 / 349

页数：9

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