4.4 Article

A new odorless one-pot synthesis of thioesters and selenoesters promoted by Rongalite®

Journal

TETRAHEDRON
Volume 66, Issue 37, Pages 7384-7388

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2010.07.023

Keywords

Rongalite (R); Acylation; Disulfides; Anhydrides; Thioesters; Selenoesters

Funding

  1. National Key Technology RD Program [2007BAI34B00]
  2. Technology Program of Zhejiang Province [2009C31159]
  3. Natural Science Foundation [Y4080107]

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Rongalite (R) promotes cleavage of diaryl disulfides generating chalcogenolate anions that then undergo facile acylation with anhydrides in the presence of CsF to afford thioesters (3) with good to excellent yields. By using the present protocol, 5-arylthio-5-oxopentanoic acid (4) can be facilely prepared. The important features of the methodology are broad substrate scope, simple operation, and no requirement for metal catalysts. It is noteworthy that acylations of diphenyl diselane with anhydrides are also conducted smoothly to afford selenoesters (5) in good yields under the standard conditions. (C) 2010 Elsevier Ltd. All rights reserved.

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