Literature DB >> 5263758

Carbon-13 nuclear magnetic resonance: naturally occurring nucleosides.

A J Jones, M W Winkley, D M Grant, R K Robins.   

Abstract

The natural-abundance carbon-13 nuclear magnetic resonance spectra of the naturally occuring pyrimidine and purine nucleosides have been determined and completely analyzed. The carbon-13 chemical shifts obtained provide information on the electronic structure and qualitatively at least correlate well with the known chemical reactivity of these molecules. The carbon-13 shifts are in general far more informative than proton shifts for structural analysis of the nucleosides.

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Year:  1970        PMID: 5263758      PMCID: PMC286185          DOI: 10.1073/pnas.65.1.27

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  1 in total

1.  Natural-abundance C nuclear magnetic resonance spectra of medium-molecular-weight organic compounds.

Authors:  F J Weigert; M Jautelat; J D Roberts
Journal:  Proc Natl Acad Sci U S A       Date:  1968-08       Impact factor: 11.205

  1 in total
  3 in total

1.  A conformational study of adenylyl-(3',5')-adenosine and adenylyl-(2',5')-adenosine in aqueous solution by carbon-13 magnetic resonance spectroscopy.

Authors:  T Schleich; B P Cross; I C Smith
Journal:  Nucleic Acids Res       Date:  1976-02       Impact factor: 16.971

2.  Nuclear magnetic resonance spectroscopy: 13C spectra of some common nucleotides.

Authors:  D E Dorman; J D Roberts
Journal:  Proc Natl Acad Sci U S A       Date:  1970-01       Impact factor: 11.205

3.  β-Cyanuryl Ribose, β-Barbituryl Ribose, and 6-Azauridine as Uridine Mimetics.

Authors:  Helaneh Salameh; Michal Afri; Hugo E Gottlieb; Bilha Fischer
Journal:  ACS Omega       Date:  2020-11-25
  3 in total

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