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

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 journal › Article › Research › peer-review

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 language	English
Pages (from-to)	339-341
Number of pages	3
Journal	Journal of the Chemical Society, Chemical Communications
Issue number	8
Publication status	Published - 1980
Externally published	Yes

Cite this

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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, Chemical Communications",

issn = "0022-4936",

publisher = "The Royal Society of Chemistry",

number = "8",

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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

AN - SCOPUS:37049094954

SP - 339

EP - 341

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

SN - 0022-4936

IS - 8

ER -

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

Abstract

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