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Successful oxidation of a key thiazoline intermediate allows an efficient synthesis of tiazofurin in four steps from commercially available 1′-acetoxy-2′,3′,5′-tri-O-benzoyl-β-D- ribofuranose. © 2002 Elsevier Science Ltd. All rights reserved.

Original publication

DOI

10.1016/S0040-4039(02)01470-3

Type

Journal article

Journal

Tetrahedron Letters

Publication Date

09/09/2002

Volume

43

Pages

6561 - 6562