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A Very Mild, Catalytic and Versatile Procedure for α-Oxidation of Ketone Silyl Enol Ethers Using (salen)Manganese(III) Complexes; A New, Chiral Complex Giving Asymmetric Induction. A Possible Model for Selective Biochemical Oxidative Reactions Through Eno

DOI: 10.1039/c39920000172

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 172 - 173 (1992)

Update date:2022-08-04

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Authors:

Reddy, D. ReddeppaReddy, D. Reddeppa

Thornton, Edward R.Thornton, Edward R.

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Article abstract of DOI:10.1039/c39920000172

Facile, catalytic, selective (racemic and asymmetric) oxidation of ketone silyl enol ethers to give α-oxygenated products proceeds well under very mild, aprotic conditions using a racemic (salen)manganese(III) complex View More

Products guided by the article

Product name:1(2H)-Naphthalenone, 3,4-dihydro-2-[(trimethylsilyl)oxy]-

Cas No:140134-32-3

140134-32-3

R&D Labs maybe for 140134-32-3

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