NMR Conformation of (−)-β-d-Aristeromycin and Its 2‘-Deoxy and 3‘-Deoxy Counterparts in Aqueous Solution-Reference-Cited by-同舟云学术

NMR Conformation of (−)-β-d-Aristeromycin and Its 2‘-Deoxy and 3‘-Deoxy Counterparts in Aqueous Solution

Published:1998-07-15 Issue:16 Volume:63 Page:5447-5462
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Thibaudeau C.¹,Kumar A.¹,Bekiroglu S.¹,Matsuda A.¹,Marquez V. E.¹,Chattopadhyaya J.¹

Affiliation:

1. Department of Bioorganic Chemistry, Box 581, Biomedical Center, University of Uppsala, S-751 23 Uppsala, Sweden, Laboratory of Medicinal Chemistry, DPT, DCT, National Cancer Institute, NIH, Bethesda, Maryland 20892, and Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo 060, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo980364y

Reference72 articles.

1. STREPTOMYCES CITRICOLOR NOV. SP. AND A NEW ANTIBIOTIC, ARISTEROMYCIN

2. Carbocyclic nucleosides

3. How do the gauche and anomeric effects drive the pseudorotational equilibrium of the pentofuranose moiety of nucleosides?

4. How does the steric effect drive the sugar conformation in the 3′-C-branched nucleosides?

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