Favorski type rearrangement in the lead tetraacetate oxidation of cycloalkanones

Article abstract of DOI:10.1080/00397919608003716

The cycloalkanones (1a-1f) have been converted into their corresponding cycloalkane carboxylates (2a-2f) by a lead(IV) acetate promoted rearrangement in presence of perchloric acid in triethyl orthoformate.

Full text of DOI:10.1080/00397919608003716

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Favorski Type
Rearrangement in the Lead
Tetraacetate Oxidation of
Cycloalkanones
Felix Mathew a & Bekington Myrboh a
a Department of Chemistry, North-Eastern Hill
University Shillong, Meghalaya, 793003, India
Available online: 21 Aug 2006
To cite this article: Felix Mathew & Bekington Myrboh (1996): Favorski Type
Rearrangement in the Lead Tetraacetate Oxidation of Cycloalkanones, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 26:6, 1097-1101
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