One-step synthesis of α,β-unsaturated ketones by the reaction of enol acetates with allyl methyl carbonate catalyzed by palladium and tin compounds

Jiro Tsuji; Ichiro Minami; Isao Shimizu

doi:10.1016/S0040-4039(00)94161-3

One-step synthesis of α,β-unsaturated ketones by the reaction of enol acetates with allyl methyl carbonate catalyzed by palladium and tin compounds

Jiro Tsuji^*, Ichiro Minami, Isao Shimizu

^*この研究の対応する著者

研究成果: Article › 査読

39 被引用数 (Scopus)

抄録

Enol acetates derived from saturated ketones are converted to α,β-unsaturated ketones by heating with allyl methyl carbonate in MeCN by bimetallic catalysis of palladium-phosphine complex and tin methoxide.

本文言語	English
ページ（範囲）	5639-5640
ページ数	2
ジャーナル	Tetrahedron Letters
巻	24
号	50
DOI	https://doi.org/10.1016/S0040-4039(00)94161-3
出版ステータス	Published - 1983

ASJC Scopus subject areas

生化学
有機化学
創薬

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10.1016/S0040-4039(00)94161-3

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引用スタイル

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abstract = "Enol acetates derived from saturated ketones are converted to α,β-unsaturated ketones by heating with allyl methyl carbonate in MeCN by bimetallic catalysis of palladium-phosphine complex and tin methoxide.",

author = "Jiro Tsuji and Ichiro Minami and Isao Shimizu",

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doi = "10.1016/S0040-4039(00)94161-3",

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AU - Tsuji, Jiro

AU - Minami, Ichiro

AU - Shimizu, Isao

PY - 1983

Y1 - 1983

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AB - Enol acetates derived from saturated ketones are converted to α,β-unsaturated ketones by heating with allyl methyl carbonate in MeCN by bimetallic catalysis of palladium-phosphine complex and tin methoxide.

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