Direct synthesis of pyrrole nucleosides by the stereospecific sodium salt glycosylation procedure
Author:
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570240361/fullpdf
Reference24 articles.
1. Total synthesis of certain 2-, 6-mono- and 2,6-disubstituted-tubercidin derivatives. Synthesis of tubercidin via the sodium salt glycosylation procedure
2. Synthesis of 2'-deoxytubercidin, 2'-deoxyadenosine, and related 2'-deoxynucleosides via a novel direct stereospecific sodium salt glycosylation procedure
3. Synthesis and antiviral/antitumor activities of certain 3-deazaguanine nucleosides and nucleotides
4. Synthesis and biological activity of certain 6-substituted and 2,6-disubstituted 2'-deoxytubercidins prepared via the stereospecific sodium salt glycosylation procedure
5. A new synthesis of certain 7-(β-D-ribofuranosyl) and 7-{2-deoxy-β-D-ribofuranosyl) derivatives of 3-deazaguanine via the sodium salt glycosylation procedure
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