A new synthesis of inosine from 5-amino-1-beta-D-ribofuranosyl-4-imidazole-carboxamide.

Abstract:

:Inosine was prepared (15% yield) by treatment of 5-amino-1-beta-D-ribofuranosyl-4-imidazolecarboxamide (AICA-riboside) with chloroform in the presence of sodium methoxide. This ring closure can be reasonably explained by assuming the formation of dichlorocarbene from chloroform and alkali. Carbon tetrachloride or hexachloroethane as a carbene source was more effective for the ring closure of AICA-riboside, giving inosine in 48% and 51% yields respectively.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Okutsu M,Yamazaki A

doi

10.1093/nar/3.1.231

keywords:

subject

Has Abstract

pub_date

1976-01-01 00:00:00

pages

231-5

issue

1

eissn

0305-1048

issn

1362-4962

journal_volume

3

pub_type

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