Conformational analysis of 3'-deoxy-beta-D-ribonucleosides using 1D-nOe difference spectroscopy (vol 15, pg 1595, 1996)

DC FieldValueLanguage
dc.contributor.authorKumar, A
dc.contributor.authorKatti, SB
dc.contributor.authorRosemeyer, H
dc.contributor.authorSeela, F
dc.date.accessioned2021-12-23T16:13:21Z-
dc.date.available2021-12-23T16:13:21Z-
dc.date.issued1997
dc.identifier.issn07328311
dc.identifier.urihttps://osnascholar.ub.uni-osnabrueck.de/handle/unios/10523-
dc.description.abstractThe results of PMR studies on 3'-deoxy-beta-D-ribonucleosides (1a-d) reveals that the sugar puckering is predominantly in N state with g+ conformation of the 5'-CH2OH group. Except in 1a, nucleobases in other nucleosides favour anti conformation.
dc.language.isoen
dc.publisherMARCEL DEKKER INC
dc.relation.ispartofNUCLEOSIDES & NUCLEOTIDES
dc.subjectBiochemistry & Molecular Biology
dc.subjectMODIFIED NUCLEOSIDES
dc.titleConformational analysis of 3'-deoxy-beta-D-ribonucleosides using 1D-nOe difference spectroscopy (vol 15, pg 1595, 1996)
dc.typeerratum
dc.identifier.doi10.1080/07328319708001367
dc.identifier.isiISI:A1997XC97600013
dc.description.volume16
dc.description.issue4
dc.description.startpage507
dc.description.endpage513
dc.publisher.place270 MADISON AVE, NEW YORK, NY 10016
dcterms.isPartOf.abbreviationNucleosides Nucleotides
crisitem.author.deptInstitut für Chemie neuer Materialien-
crisitem.author.deptidinstitute11-
crisitem.author.parentorgFB 05 - Biologie/Chemie-
crisitem.author.grandparentorgUniversität Osnabrück-
crisitem.author.netidRoHe783-
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