Download PDF
Synthesis 2000; 2000(2): 223-225
DOI: 10.1055/s-2000-6262
short paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Oxidation in Fluoro Alcohols: Mild and Efficient Preparation of Disulfides from Thiols

Venkitasamy Kesavan* , Danièle Bonnet-Delpon, Jean-Pierre Bégué
  • *Laboratoire BIOCIS associé au CNRS, Centre d'Etudes Pharmaceutiques, Rue J. B. Clément, 92296 Châtenay-Malabry, France; Fax +33 (1) 46 83 57 40; E-mail: jean-pierre.begue@cep.u-psud.fr
Further Information

Publication History

Publication Date:
31 December 2000 (online)

  PDF Download  Permissions and Reprints All articles of this category

Quantitative oxidative conversion of thiols to disulfides was effected by aqueous 30% H2O2 in trifluoroethanol at ambient temperature under neutral conditions.

thiols - disulfides - oxidative coupling - hydrogen peroxide - fluoro alcohols

      >