Convenient synthesis of 4-C-branched lactones and 3'-C-branched 2',3'- dideoxynucleosides

Article abstract of DOI:10.1080/07328319608002436

The regio- and stereoselective photocatalysed addition of 2-propanol and cyclopentanol to (5S)-hydroxymethylfuran-2(5H)-one (1) gave 4-C-branched lactones 2 and 3 after selective silylations. The lactones 2 and 3 were radically deoxygenated affording lact

Full text of DOI:10.1080/07328319608002436

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Nucleosides and Nucleotides
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Convenient Synthesis of 4-C-Branched
Lactones and 3′-C-Branched 2′,3′-
Dideoxynucleosides
Jesper Wengel a , Kirsten Østergaard a & Anders Hager a
a Department of Chemistry , Odense University , DK-5230, Odense M,
Denmark
Published online: 22 Aug 2006.
To cite this article: Jesper Wengel , Kirsten Østergaard & Anders Hager (1996) Convenient Synthesis
of 4-C-Branched Lactones and 3′-C-Branched 2′,3′-Dideoxynucleosides, Nucleosides and Nucleotides,
15:7-8, 1361-1368, DOI: 10.1080/07328319608002436
To link to this article: http://dx.doi.org/10.1080/07328319608002436
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