ANCHIMERIC ASSISTANCE OF A 5'-O-CARBONYL FUNCTION FOR INVERSION OF CONFIGURATION AT THE 3'-CARBON ATOM OF 2'-DEOXYADENOSINE - SYNTHESIS OF 3'-AZIDO-2',3'-DIDEOXYADENOSINE AND 3'-AZIDO-2',3'-DIDEOXYINOSINE

被引：28

作者：

HERDEWIJN, PAM ^{[1
]}

机构：

[1] CATHOLIC UNIV LEUVEN, INST PHARMACEUT, B-3000 LOUVAIN, BELGIUM

来源：

JOURNAL OF ORGANIC CHEMISTRY | 1988年 / 53卷 / 21期

关键词：

D O I：

10.1021/jo00256a027

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：5050 / 5053

页数：4

共 20 条

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[6] NUCLEIC-ACID RELATED-COMPOUNDS .45. A DEOXYGENATIVE [1,2]-HYDRIDE SHIFT REARRANGEMENT CONVERTING CYCLIC CIS-DIOL MONOTOSYLATES TO INVERTED SECONDARY ALCOHOLS
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[7] SYNTHESIS AND ANTI-HIV ACTIVITY OF VARIOUS 2'-SUBSTITUTED AND 3'-SUBSTITUTED 2',3'-DIDEOXYADENOSINES - A STRUCTURE ACTIVITY ANALYSIS
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[J]. JOURNAL OF MEDICINAL CHEMISTRY, 1987, 30 (11) : 2131 - 2137
[8] 3'-SUBSTITUTED 2',3'-DIDEOXYNUCLEOSIDE ANALOGS AS POTENTIAL ANTI-HIV (HTLV-III/LAV) AGENTS
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[10] IKEHARA M, 1971, CHEM PHARM BULL, V19, P538

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