NUCLEOSIDES .9. DIRECT SYNTHESIS OF URACIL NUCLEOSIDES

被引:11
作者
ROGERS, GT
ULBRICHT, TL
机构
[1] Twyford Laboratories Ltd., London N.W.10, Elveden Road
来源
JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC | 1969年 / 18期
关键词
D O I
10.1039/j39690002450
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The direct synthesis of uracil nucleosides results from the reaction of uracil with a glycosyl halide in the presence of mercuric cyanide. In this way, uracil can be converted into N(3)-(2′,3′,4′,6′-tetra-O-acetyl-β-D- glucopyranosyl)uracil (I) and N(1)N(3)-bis-(2′,3′,4′,6′-tetra-O-acetyl-β-D- glucopyranosyl)uracil (III). Either (I) or (III) can be obtained as the main product in high yield by choice of appropriate reaction conditions; (III) is formed from (I) via the N(3)O(6)-bisglucoside (II). A convenient synthesis of 2′,3′,5′-tri-O-acetyluridine illustrates the usefulness of the method.
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页码:2450 / &
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