145828-13-3Relevant articles and documents
Stereocontrolled de novo synthesis of β-2'-deoxyribonucleosides
Park,Rizzo
, p. 6092 - 6093 (1996)
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Synthesis of 2'-Deoxyribonucleosides: ?-3',5'-Di-O-benzoylthymidine [ Thymidine, 3',5'-dibenzoate ]
Prudhomme, Daniel R.,Park, Minnie,Wang, Zhiwei,Buck, Jason R.,Rizzo, Carmelo J.,Chambournier, Gilles,Djung, Jane,Hart, David J.
, p. 162 - 162 (2017/09/30)
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Radical Rearrangement of 2-O-(Diphenylphosphoryl)glycosyl Bromides. A New Synthesis for 2-Deoxy Disaccharides and 2-Deoxy Ribonucleosides
Koch, Andreas,Lamberth, Clemens,Wetterich, Frank,Giese, Bernd
, p. 1083 - 1089 (2007/10/02)
2-Deoxy-1-O-diphenylphosphoryl glycosides react with nucleophiles under mild conditions giving access to 2-deoxy disaccharides and nucleosides.The intermediate 2-deoxy-1-O-diphenylphosphoryl compounds were generated in situ by a radical 2 -> 1 migration of the phosphate ester group.This is the first observation of a rearrangement of a phosphate ester in radicals.ESR experiments and quenching of the radical at C2 by tin hydride or tin deuteride were used to detect the intermediates and to prove their structure.