Halogenation of tubercidin by N-halosuccinimides. A direct route to 5-bromotubercidin, a reversible inhibitor of RNA synthesis in eukaryotic cells.

Abstract:

:Tubercidin may be directly brominated by reaction with N-bromosuccinimide in DMF to give 5-bromotubercidin, a reversible inhibitor of RNA synthesis. When buffered with potassium acetate the major product is 6-bromotubercidin. 5,6-Dibromotubercidin is formed in minor amounts under both conditions. N-Chlorosuccinimide and tubercidin give 5-chlorotubercidin and 5,6-dichlorotubercidin.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Bergstrom DE,Brattesani AJ

doi

10.1093/nar/8.24.6213

subject

Has Abstract

pub_date

1980-12-20 00:00:00

pages

6213-9

issue

24

eissn

0305-1048

issn

1362-4962

journal_volume

8

pub_type

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