HALOGENATION OF TUBERCIDIN BY N-HALOSUCCINIMIDES - A DIRECT ROUTE TO 5-BROMOTUBERCIDIN, A REVERSIBLE INHIBITOR OF RNA-SYNTHESIS IN EUKARYOTIC CELLS

被引：21

作者：

BERGSTROM, DE

BRATTESANI, AJ

机构：

来源：

NUCLEIC ACIDS RESEARCH | 1980年 / 8卷 / 24期

关键词：

D O I：

10.1093/nar/8.24.6213

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：

引用

页码：6213 / 6219

页数：7

共 12 条

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[6] PYRROLOPYRIMIDINE NUCLEOSIDES .I. SYNTHESIS OF 4-SUBSTITUTED 7-(BETA-D-RIBOFURANOSYL)PYRROLO[2,3-D]PYRIMIDINES FROM TUBERCIDIN [J].

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[7]

Goodman L., 1974, BASIC PRINCIPLES NUC, V1, P93

[8] PYRROLOPYRIMIDINE NUCLEOSIDES .4. SYNTHESIS OF CERTAIN 4,5-DISUBSTITUTED-7-(BETA-D-RIBOFURANOSYL)PYRROLO[2,3-D]PYRIMIDINES RELATED TO PYRROLO[2,3-D]PYRIMIDINE NUCLEOSIDE ANTIBIOTICS [J].

HINSHAW, BC ;

GERSTER, JF ;

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TOWNSEND, LB .

JOURNAL OF HETEROCYCLIC CHEMISTRY, 1969, 6 (02) :215-&

[9] N-BROMOSUCCINIMIDE-DIMETHYLFORMAMIDE - MILD, SELECTIVE NUCLEAR MONO-BROMINATION REAGENT FOR REACTIVE AROMATIC-COMPOUNDS [J].

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[10]

REICH E, 1972, VIROLOGY, V50, P630

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