Carbon-13 nuclear magnetic resonance study of tyrosine titrations

Raymond S. Norton, J. Howard Bradbury

Research output: Contribution to journalArticleResearchpeer-review

20 Citations (Scopus)

Abstract

The ionization of the phenolic hydroxy-groups of tyrosines in peptides and proteins in alkaline solutions produces appreciable shifts of the C χ, Cε, and Cγ (1) carbon-13 nuclear magnetic resonances, from which the apparent pK values of tyrosine residues can be obtained.

Original languageEnglish
JournalJournal of the Chemical Society, Chemical Communications
Issue number21
DOIs
Publication statusPublished - 1974
Externally publishedYes

Cite this

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title = "Carbon-13 nuclear magnetic resonance study of tyrosine titrations",
abstract = "The ionization of the phenolic hydroxy-groups of tyrosines in peptides and proteins in alkaline solutions produces appreciable shifts of the C χ, Cε, and Cγ (1) carbon-13 nuclear magnetic resonances, from which the apparent pK values of tyrosine residues can be obtained.",
author = "Norton, {Raymond S.} and Bradbury, {J. Howard}",
year = "1974",
doi = "10.1039/C3974000870b",
language = "English",
journal = "Journal of the Chemical Society - Series Chemical Communications",
issn = "0022-4936",
publisher = "The Royal Society of Chemistry",
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Carbon-13 nuclear magnetic resonance study of tyrosine titrations. / Norton, Raymond S.; Bradbury, J. Howard.

In: Journal of the Chemical Society, Chemical Communications, No. 21, 1974.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

T1 - Carbon-13 nuclear magnetic resonance study of tyrosine titrations

AU - Norton, Raymond S.

AU - Bradbury, J. Howard

PY - 1974

Y1 - 1974

N2 - The ionization of the phenolic hydroxy-groups of tyrosines in peptides and proteins in alkaline solutions produces appreciable shifts of the C χ, Cε, and Cγ (1) carbon-13 nuclear magnetic resonances, from which the apparent pK values of tyrosine residues can be obtained.

AB - The ionization of the phenolic hydroxy-groups of tyrosines in peptides and proteins in alkaline solutions produces appreciable shifts of the C χ, Cε, and Cγ (1) carbon-13 nuclear magnetic resonances, from which the apparent pK values of tyrosine residues can be obtained.

UR - http://www.scopus.com/inward/record.url?scp=37049140963&partnerID=8YFLogxK

U2 - 10.1039/C3974000870b

DO - 10.1039/C3974000870b

M3 - Article

JO - Journal of the Chemical Society - Series Chemical Communications

JF - Journal of the Chemical Society - Series Chemical Communications

SN - 0022-4936

IS - 21

ER -