Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

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