Synthesis of unsaturated carboacyclic nucleoside analogues via Mitsunobu reactions

Article abstract of DOI:10.1080/15257770008033028

2-Substituted allyl alcohols 9 and 14 were prepared starting from butane-1,2,4-triol and glycerol, respectively. Mitsunobu condensations of 9 and 14 with purine and pyrimidine bases, followed by deprotection, afforded a number of acyclonucleosides having

Full text of DOI:10.1080/15257770008033028

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Nucleosides, Nucleotides and Nucleic
Acids
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Synthesis of Unsaturated Carboacyclic
Nucleoside Analogues via Mitsunobu
Reactions
Jinfa Du a & Guangyi Wang a
a Chemistry Laboratory, ICN Pharmaceuticals, Inc., 3300 Hyland
Avenue, Costa Mesa, California, 92626, U.S.A.
Version of record first published: 24 Sep 2006.
To cite this article: Jinfa Du & Guangyi Wang (2000): Synthesis of Unsaturated Carboacyclic
Nucleoside Analogues via Mitsunobu Reactions, Nucleosides, Nucleotides and Nucleic Acids,
19:5-6, 867-879
To link to this article: http://dx.doi.org/10.1080/15257770008033028
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