C-nucleosides. Part 2. Preparation of 2-[(1R,2S,3R,4R)-2,3-dihydroxy-4-(hydroxymethyl)cyclopentyl]thiazole-4-carboxamide (‘carbocyclic’ tiazofurin) and its antipode-Reference-Cited by-同舟云学术

C-nucleosides. Part 2. Preparation of 2-[(1R,2S,3R,4R)-2,3-dihydroxy-4-(hydroxymethyl)cyclopentyl]thiazole-4-carboxamide (‘carbocyclic’ tiazofurin) and its antipode

Published:1993 Issue:1 Volume: Page:57-65
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Dishington Allan P.,Humber David C.,Stoodley Richard J.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1993/P1/P19930000057

Reference28 articles.

1. C-nucleosides. Part 1. Preparation of tiazofurin and N-substituted tiazofurins from benzyl (2′,3′,5′-tri-O-benzoyl-β-D-ribofuranosyl)penicillinate

2. Synthesis of C-glycosyl thiazoles

3. Synthesis and antiviral activity of certain thiazole C-nucleosides

4. J. G. Buchanan and R. H.Wightman, in Topics in Antibiotic Chemistry, ed. P. G. Sammes, Ellis Harwood, Chichester, 1982, vol. 6, p. 229;

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