Diastereofacial Selective Addition of Ethynylcerium Reagent and Barton−McCombie Reaction as the Key Steps for the Synthesis of C-3‘-Ethynylribonucleosides and of C-3‘-Ethynyl-2‘-deoxyribonucleosides
Author:
Affiliation:
1. Laboratoire de Chimie Organique Biologique URA 31 du CNRS, Faculté de Chimie, Université Louis Pasteur, 1 rue Blaise Pascal, 67008 Strasbourg Cedex, France
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9704568
Reference39 articles.
1. For reviews, see for instance: (a) Périgaud C.; Gosselin G.; Imbach J.L.Nucleosides Nucleotides1992,11, 903−945. (b) Herdewijn P.; Balzarini J.; De Clercq E. InAdvances in Antiviral Drug Design; De Clercq E., Ed. JAI Press, Inc. Greenwich, 1993; Vol. 1, pp 233−309.
2. An Example of Alkyne-Alkyne Interaction
3. Inhibitors of human purine nucleoside phosphorylase. Synthesis and biological activities of 8-amino-3-benzylhypoxanthine and related analogs
4. Epimerization during the acetolysis of 3-O-acetyl-5-O-benzoyl-1,2-O-isopropylidene-3-C-methyl-α-d-ribofuranose. Synthesis of 3′-C-methylnucleosides with the β-d-ribo- and α-d-arabino configurations
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