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The discovery of intramolecular stereoelectronic forces that drive the sugar conformation in nucleosides and nucleotides
Uppsala University.
Uppsala University.
1997 (English)In: NUCLEOSIDES & NUCLEOTIDES, ISSN 0732-8311, Vol. 16, no 5-6, 523-529 p.Article in journal (Other scientific) Published
Abstract [en]

This report summarizes our results(8) on how the determination of the thermodynamics of the two-state North (N,C2'-exo-C3'-endo) reversible arrow South (S,C2'-endo-C3'-exo) pseudorotational equilibrium in aqueous solution (pD 0.6 - 12.0) basing on vicinal

Place, publisher, year, edition, pages
MARCEL DEKKER INC , 1997. Vol. 16, no 5-6, 523-529 p.
Keyword [en]
PSEUDOROTATIONAL EQUILIBRIUM; PENTOFURANOSE MOIETY; COUPLING-CONSTANTS; C-NUCLEOSIDES; FURANOSE RING; LARIAT-RNA; ORIGIN; PROTON; GAUCHE; SPECTROSCOPY
Identifiers
URN: urn:nbn:se:uu:diva-27444OAI: oai:DiVA.org:uu-27444DiVA: diva2:55339
Note
Addresses: UNIV UPPSALA, CTR BIOMED, DEPT BIOORGAN CHEM, S-75123 UPPSALA, SWEDEN.Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-15

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