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A facile access to 2-deoxy-l-ribose

Authors
Publisher
Elsevier Ltd
Publication Date
Volume
12
Issue
15
Identifiers
DOI: 10.1016/s0957-4166(01)00386-x

Abstract

Abstract The title compound was prepared in five steps starting from R-(+)-5-benzyloxymethyl-5 H-furan-2-one 1 via syn-dihydroxylation of its double bond, regioselective tosylation of the 2-OH group in the thus obtained diol 2 followed by selective deoxygenation of that position.

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