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Licensed Unlicensed Requires Authentication Published by De Gruyter June 2, 2014

Total Synthesis of S-(+)-Argentilactone

  • Muhammad Saeed , Muhammad Abbas , Khalid Mohammad Khan and Wolfgang Voelter

Abstract

Asymmetrie Total Synthesis Asymmetrie total synthesis of S-(+)-argentilactone (2) was accomplished, using methyl-a-D-glucopyranoside (3) as carbohydrate template. Benzylidene acetal 5 was hydrolysed with tBuOOH/AlCl3 and further manipulated to produce the aldehyde 10. A Wittig reaction and subsequent oxidation of the anomeric position yielded the target argentilactone.

Received: 2000-12-16
Published Online: 2014-6-2
Published in Print: 2001-3-1

© 1946 – 2014: Verlag der Zeitschrift für Naturforschung

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