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NMR conformation of (-)-beta-D-aristeromycin and its 2 '-deoxy and 3 '-deoxy counterparts in aqueous solution
Uppsala University.
Uppsala University.
Uppsala University.
Uppsala University.
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1998 (English)In: JOURNAL OF ORGANIC CHEMISTRY, ISSN 0022-3263, Vol. 63, no 16, 5447-5462 p.Article in journal (Other scientific) Published
Abstract [en]

The solution conformations of aristeromycin (1), 2'-deoxyaristeromycin (2), and 3'-deoxyaristeromycin (3) have been determined from an integrated analysis of X-ray (for 1 only), NMR data (i.e., (3)J(HH) coupling constants), and ab initio calculations. One

Place, publisher, year, edition, pages
AMER CHEMICAL SOC , 1998. Vol. 63, no 16, 5447-5462 p.
Keyword [en]
HIV AIDS VIRUS; PSEUDOROTATIONAL EQUILIBRIUM; PENTOFURANOSE MOIETY; COUPLING-CONSTANTS; CRYSTAL-STRUCTURE; SUBSTITUENT ELECTRONEGATIVITIES; CARBOCYCLIC THYMIDINE; REVERSE-TRANSCRIPTASE; H-1-NMR SPECTROSCOPY; MOLECULAR-STRUCTURE
Identifiers
URN: urn:nbn:se:uu:diva-27430OAI: oai:DiVA.org:uu-27430DiVA: diva2:55325
Note
Addresses: Chattopadhyaya J, Univ Uppsala, Ctr Biomed, Dept Bioorgan Chem, Box 581, S-75123 Uppsala, Sweden. Univ Uppsala, Ctr Biomed, Dept Bioorgan Chem, S-75123 Uppsala, Sweden. NCI, NIH, DCT, DPT, Lab Med Chem, Bethesda, MD 20892 USA. Hokkaido Univ, FaAvailable from: 2008-10-17 Created: 2008-10-17 Last updated: 2011-01-14

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