A new reagent for the formation of anhydronucleosides

Article abstract of DOI:10.1080/07328319608002419

5'-O-Trityl-thymidine reacts with excess perfluorobutanesulfonyl fluoride/DBU in toluene to 5'-O-trityl-2,3'-anhydrothymidine in 75% yield. Free thymidine gives rise to 4',5'-dehydro-2,3'-anhydrothymidine and to 5'-fluoro-2,3'-anhydrothymidine.

Full text of DOI:10.1080/07328319608002419

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Nucleosides and Nucleotides
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A New Reagent for the Formation of
Anhydronucleosides
B. Bennua-Skalmowski a & H. Vorbrüggen a
a Research Laboratories, Schering AG , 13342, Berlin, Germany
Published online: 21 Aug 2006.
To cite this article: B. Bennua-Skalmowski & H. Vorbrüggen (1996) A New Reagent for the
Formation of Anhydronucleosides, Nucleosides and Nucleotides, 15:1-3, 739-742
To link to this article: http://dx.doi.org/10.1080/07328319608002419
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