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Assignment of the 13 C NMR signals of some 8‐azaadenine, 2,6‐diaminopurine and 2,6‐diamino‐8‐azapurine carbonucleosides
Author(s) -
Teijeira M.,
Terán C.,
Uriarte E.
Publication year - 1999
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/(sici)1097-458x(199908)37:8<598::aid-mrc494>3.0.co;2-6
Subject(s) - chemistry , purine , purine metabolism , dept , carbon 13 nmr , stereochemistry , hydroxymethyl , organic chemistry , enzyme
The 13 C NMR signals of various 9‐(2‐hydroxymethyl‐cyclopentyl)purines and 9‐(2‐hydroxymethylcyclo‐pentylmethyl)purines (purine = 8‐azaadenine, 2,6‐diaminopurine or 2,6‐diamino‐8‐azapurine) were fully assigned with the aid of one‐dimensional ( 1 H, 1 H– 1 H NOE, DEPT) and two‐dimensional (HMQC and HMBC) NMR experiments. Copyright © 1999 John Wiley & Sons, Ltd.