Manganese(III) acetate oxidation of alkyl substituted 1- (phenylsulfonyl)indoles

Article abstract of DOI:10.1080/00397919408011507

Methyl substituted 1-(phenylsulfonyl)indoles undergo tandem oxidation of the indoline ring and a C-2 methyl group. If there is no alkyl substituent at the C-2 position, nuclear acetoxylation can occur to afford oxindoles.

Full text of DOI:10.1080/00397919408011507

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Manganese(III) Acetate
Oxidation of Alkyl Substituted
1-(Phenylsulfonyl)indoles
Daniel M. Ketcha a , Qin Zhou a & David Grossie a
a Department of Chemistry , Wright State
University , Dayton, Ohio, 45435
Published online: 04 Jan 2007.
To cite this article: Daniel M. Ketcha , Qin Zhou & David Grossie (1994) Manganese(III)
Acetate Oxidation of Alkyl Substituted 1-(Phenylsulfonyl)indoles, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 24:4, 565-574, DOI: 10.1080/00397919408011507
To link to this article: http://dx.doi.org/10.1080/00397919408011507
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