Reduction vs. acetalisation of some carbonyl compounds by means of methylselenol and Lewis acids

A. Cravador, A. Krief, L. Hevesi

Résultats de recherche: Contribution à un journal/une revueArticle

Résumé

Aliphatic ketones and aromatic carbonyl compounds on reaction with methylselenol and a Lewis acid, are shown to undergo acetalisation and/or reduction to methyl selenide, the unexpected reduction reaction being predominant in most cases.
langue originaleAnglais
Pages (de - à)451
Nombre de pages1
journalJournal of the Chemical Society, Chemical Communications
Numéro de publication10
étatPublié - 1 janv. 1980

Empreinte digitale

Lewis Acids
Ketones
methaneselenol

Citer ceci

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title = "Reduction vs. acetalisation of some carbonyl compounds by means of methylselenol and Lewis acids",
abstract = "Aliphatic ketones and aromatic carbonyl compounds on reaction with methylselenol and a Lewis acid, are shown to undergo acetalisation and/or reduction to methyl selenide, the unexpected reduction reaction being predominant in most cases.",
author = "A. Cravador and A. Krief and L. Hevesi",
year = "1980",
month = "1",
day = "1",
language = "English",
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journal = "J. Chem. Soc.",
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Reduction vs. acetalisation of some carbonyl compounds by means of methylselenol and Lewis acids. / Cravador, A.; Krief, A.; Hevesi, L.

Dans: Journal of the Chemical Society, Chemical Communications, Numéro 10, 01.01.1980, p. 451.

Résultats de recherche: Contribution à un journal/une revueArticle

TY - JOUR

T1 - Reduction vs. acetalisation of some carbonyl compounds by means of methylselenol and Lewis acids

AU - Cravador, A.

AU - Krief, A.

AU - Hevesi, L.

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Y1 - 1980/1/1

N2 - Aliphatic ketones and aromatic carbonyl compounds on reaction with methylselenol and a Lewis acid, are shown to undergo acetalisation and/or reduction to methyl selenide, the unexpected reduction reaction being predominant in most cases.

AB - Aliphatic ketones and aromatic carbonyl compounds on reaction with methylselenol and a Lewis acid, are shown to undergo acetalisation and/or reduction to methyl selenide, the unexpected reduction reaction being predominant in most cases.

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JO - J. Chem. Soc.

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