Antimony(III) chloride as an efficient catalyst for palladium-catalyzed hydrophenylation of α,β-unsaturated ketones and aldehydes

Chan Sik Cho; Shin ichi Motofusa; Sakae Uemura

doi:10.1016/0040-4039(94)88333-5

Antimony(III) chloride as an efficient catalyst for palladium-catalyzed hydrophenylation of α,β-unsaturated ketones and aldehydes

Chan Sik Cho, Shin ichi Motofusa, Sakae Uemura

Department of Applied Chemistry

Kyoto University

Research output: Contribution to journal › Article › peer-review

30 Scopus citations

Abstract

A remarkable catalytic effect of antimony(III) chloride was disclosed in palladium-catalyzed hydrophenylation of α,β-unsaturated ketones and aldehydes (Michael-type conjugate addition) with sodium tetraphenylborate in acetic acid at 25°C.

Original language	English
Pages (from-to)	1739-1742
Number of pages	4
Journal	Tetrahedron Letters
Volume	35
Issue number	11
DOIs	https://doi.org/10.1016/0040-4039(94)88333-5
State	Published - 14 Mar 1994

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title = "Antimony(III) chloride as an efficient catalyst for palladium-catalyzed hydrophenylation of α,β-unsaturated ketones and aldehydes",

abstract = "A remarkable catalytic effect of antimony(III) chloride was disclosed in palladium-catalyzed hydrophenylation of α,β-unsaturated ketones and aldehydes (Michael-type conjugate addition) with sodium tetraphenylborate in acetic acid at 25°C.",

author = "Cho, {Chan Sik} and Motofusa, {Shin ichi} and Sakae Uemura",

year = "1994",

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T1 - Antimony(III) chloride as an efficient catalyst for palladium-catalyzed hydrophenylation of α,β-unsaturated ketones and aldehydes

AU - Cho, Chan Sik

AU - Motofusa, Shin ichi

AU - Uemura, Sakae

PY - 1994/3/14

Y1 - 1994/3/14

N2 - A remarkable catalytic effect of antimony(III) chloride was disclosed in palladium-catalyzed hydrophenylation of α,β-unsaturated ketones and aldehydes (Michael-type conjugate addition) with sodium tetraphenylborate in acetic acid at 25°C.

AB - A remarkable catalytic effect of antimony(III) chloride was disclosed in palladium-catalyzed hydrophenylation of α,β-unsaturated ketones and aldehydes (Michael-type conjugate addition) with sodium tetraphenylborate in acetic acid at 25°C.

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U2 - 10.1016/0040-4039(94)88333-5

DO - 10.1016/0040-4039(94)88333-5

M3 - Article

AN - SCOPUS:0028266753

SN - 0040-4039

VL - 35

SP - 1739

EP - 1742

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 11

ER -

Antimony(III) chloride as an efficient catalyst for palladium-catalyzed hydrophenylation of α,β-unsaturated ketones and aldehydes

Abstract

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