Hypervalent iodine in synthesis. XXIV: A facile method for the preparation of arylsulfinic esters: Oxidation of disulfides or thiophenols by phenyliodine(III) bis(trifluoroacetate) in the presence of alcohols

Article abstract of DOI:10.1080/00397919708006060

Arylsulfinic esters were prepared by the oxidation of diaryl disulfides or thiophenols with phenyliodine(III) bis(trifluoroacetate) in the presence of alcohols.

Full text of DOI:10.1080/00397919708006060

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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Hypervalent Iodine in Synthesis
XXIV: A Facile Method for the
Preparation of Arylsulfinic
Esters: Oxidation of Disulfides
or Thiophenols by Phenyliodine
(III) bis(Trifluoroacetate) in the
Presence of Alcohols
Min Xia a & Zhen-Chu Chen a
a Department of Chemistry , Hangzhou University ,
Hangzhou, P. R. China
Published online: 22 Aug 2006.
To cite this article: Min Xia & Zhen-Chu Chen (1997) Hypervalent Iodine in Synthesis
XXIV: A Facile Method for the Preparation of Arylsulfinic Esters: Oxidation of Disulfides
or Thiophenols by Phenyliodine (III) bis(Trifluoroacetate) in the Presence of Alcohols,
Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 27:8, 1321-1326, DOI: 10.1080/00397919708006060
To link to this article: http://dx.doi.org/10.1080/00397919708006060
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