Acetals oxidation into esters with electrophilic halogens

Article abstract of DOI:10.1080/00397919208019097

A preparative oxidation of dioxolanes groups into esters is described. Among the different electophilic halogens and solvents which have been tested, ICl/H₂O in methylene chloride and Br₂/H₂O in acetonitrile gave the best results.

Full text of DOI:10.1080/00397919208019097

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Acetals Oxidation Into Esters
with Electrophilic Halogens
Anne-Françoise Mingotaud a , Dominique Florentin a
& Andrée Marquet a
a Laboratoire de Chimie Organique Biologique-
URA CNRS 493, Université Paris, 6, 4 place Jussieu,
75252, Paris, Cédex 05
Version of record first published: 23 Sep 2006.
To cite this article: Anne-Françoise Mingotaud , Dominique Florentin & Andrée
Marquet (1992): Acetals Oxidation Into Esters with Electrophilic Halogens, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 22:16, 2401-2404
To link to this article: http://dx.doi.org/10.1080/00397919208019097
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