Novel oxidation products from guanine nucleosides reacted with dimethyldioxirane.

Jerry Davies; John Malone; Derek Boyd; B.K. Stein; C. Stevenson; S. Kumar; J. Lyle; L. Cosby; Narain Sharma; A.P. Hunter

doi:10.1039/b201418c

Novel oxidation products from guanine nucleosides reacted with dimethyldioxirane.

Jerry Davies
, John Malone
, Derek Boyd
, B.K. Stein
, C. Stevenson
, S. Kumar
, J. Lyle
, L. Cosby
, Narain Sharma
, A.P. Hunter

Research output: Contribution to journal › Article › peer-review

4 Citations (Scopus)

Abstract

Treatment of guanosine or 2'-deoxyguanosine with dimethyldioxirane, followed by heating in aqueous solution, generates respectively 4-amidinocarbamoyl-5-hydroxyimidazole (1) or its 2-(2,3,4-trihydroxybutyl) derivative (2).

Original language	English
Pages (from-to)	1378-1379
Number of pages	2
Journal	Chemical Communications
Volume	2002(13)
Issue number	13
DOIs	https://doi.org/10.1039/b201418c
Publication status	Published - May 2002

ASJC Scopus subject areas

General Chemistry

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10.1039/b201418c

Cite this

@article{d2e0f0d534454561a4a034f7a9264baf,

title = "Novel oxidation products from guanine nucleosides reacted with dimethyldioxirane.",

abstract = "Treatment of guanosine or 2'-deoxyguanosine with dimethyldioxirane, followed by heating in aqueous solution, generates respectively 4-amidinocarbamoyl-5-hydroxyimidazole (1) or its 2-(2,3,4-trihydroxybutyl) derivative (2).",

author = "Jerry Davies and John Malone and Derek Boyd and B.K. Stein and C. Stevenson and S. Kumar and J. Lyle and L. Cosby and Narain Sharma and A.P. Hunter",

year = "2002",

month = may,

doi = "10.1039/b201418c",

language = "English",

volume = "2002(13)",

pages = "1378--1379",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "13",

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TY - JOUR

T1 - Novel oxidation products from guanine nucleosides reacted with dimethyldioxirane.

AU - Davies, Jerry

AU - Malone, John

AU - Boyd, Derek

AU - Stein, B.K.

AU - Stevenson, C.

AU - Kumar, S.

AU - Lyle, J.

AU - Cosby, L.

AU - Sharma, Narain

AU - Hunter, A.P.

PY - 2002/5

Y1 - 2002/5

N2 - Treatment of guanosine or 2'-deoxyguanosine with dimethyldioxirane, followed by heating in aqueous solution, generates respectively 4-amidinocarbamoyl-5-hydroxyimidazole (1) or its 2-(2,3,4-trihydroxybutyl) derivative (2).

AB - Treatment of guanosine or 2'-deoxyguanosine with dimethyldioxirane, followed by heating in aqueous solution, generates respectively 4-amidinocarbamoyl-5-hydroxyimidazole (1) or its 2-(2,3,4-trihydroxybutyl) derivative (2).

UR - https://www.scopus.com/pages/publications/0036087127

U2 - 10.1039/b201418c

DO - 10.1039/b201418c

M3 - Article

SN - 1359-7345

VL - 2002(13)

SP - 1378

EP - 1379

JO - Chemical Communications

JF - Chemical Communications

IS - 13

ER -

Novel oxidation products from guanine nucleosides reacted with dimethyldioxirane.

Abstract

ASJC Scopus subject areas

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