13C N.M.R. spin-lattice relaxation time measurements determining the major tautomer of 1-methylisoguanosine in solution

Raymond S. Norton, Richard P. Gregson, Ronald J. Quinn

Research output: Contribution to journalArticleResearchpeer-review

12 Citations (Scopus)

Abstract

Analysis of the contributions of 13C-1H dipolar interactions to the 13C n.m.r. spin-lattice relaxation times of the quaternary carbons of 1-methylisoguanosine establishes that the predominant tautomer in solution is the 2-keto, 6-amino form.

Original languageEnglish
Pages (from-to)339-341
Number of pages3
JournalJournal of the Chemical Society, Chemical Communications
Issue number8
Publication statusPublished - 1980
Externally publishedYes

Cite this

@article{f2fd19fbc0b341b9aef2a19ee7403079,
title = "13C N.M.R. spin-lattice relaxation time measurements determining the major tautomer of 1-methylisoguanosine in solution",
abstract = "Analysis of the contributions of 13C-1H dipolar interactions to the 13C n.m.r. spin-lattice relaxation times of the quaternary carbons of 1-methylisoguanosine establishes that the predominant tautomer in solution is the 2-keto, 6-amino form.",
author = "Norton, {Raymond S.} and Gregson, {Richard P.} and Quinn, {Ronald J.}",
year = "1980",
language = "English",
pages = "339--341",
journal = "Journal of the Chemical Society - Series Chemical Communications",
issn = "0022-4936",
publisher = "The Royal Society of Chemistry",
number = "8",

}

13C N.M.R. spin-lattice relaxation time measurements determining the major tautomer of 1-methylisoguanosine in solution. / Norton, Raymond S.; Gregson, Richard P.; Quinn, Ronald J.

In: Journal of the Chemical Society, Chemical Communications, No. 8, 1980, p. 339-341.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

T1 - 13C N.M.R. spin-lattice relaxation time measurements determining the major tautomer of 1-methylisoguanosine in solution

AU - Norton, Raymond S.

AU - Gregson, Richard P.

AU - Quinn, Ronald J.

PY - 1980

Y1 - 1980

N2 - Analysis of the contributions of 13C-1H dipolar interactions to the 13C n.m.r. spin-lattice relaxation times of the quaternary carbons of 1-methylisoguanosine establishes that the predominant tautomer in solution is the 2-keto, 6-amino form.

AB - Analysis of the contributions of 13C-1H dipolar interactions to the 13C n.m.r. spin-lattice relaxation times of the quaternary carbons of 1-methylisoguanosine establishes that the predominant tautomer in solution is the 2-keto, 6-amino form.

UR - http://www.scopus.com/inward/record.url?scp=37049094954&partnerID=8YFLogxK

M3 - Article

SP - 339

EP - 341

JO - Journal of the Chemical Society - Series Chemical Communications

JF - Journal of the Chemical Society - Series Chemical Communications

SN - 0022-4936

IS - 8

ER -