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Suppression of racemization during the diastereoselective C-3 functionalization of 5-hydroxymethyl-2-phenylthio-2-(5H)-furanones

✍ Scribed by Julie A. Wurster; Lawrence J. Wilson; Gregory T. Morin; Dennis Liotta


Publisher
Elsevier Science
Year
1992
Tongue
French
Weight
296 KB
Volume
33
Category
Article
ISSN
0040-4039

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## Abstract 3,4‐Dichloro‐2(5__H__)‐furanone, which has been prepared efficiently from mucochloric acid, has been transformed selectively into 4‐aryl‐3‐chloro‐2(5__H__)‐furanones either by Suzuki‐ or Stille‐type reactions. These monochloro derivatives have been used as precursors either to (__Z__)‐4