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-beta-D-ribofuranose. (C) 2002 Elsevier Science Ltd. All rights reserved.
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-beta-D-ribofuranose. (C) 2002 Elsevier Science Ltd. All rights reserved.