Palladium-catalyzed cross-coupling reactions between 1-alkynylstibines and acyl chlorides
N Kakusawa, K Yamaguchi, J Kurita, T Tsuchiya
Index: Kakusawa, Naoki; Yamaguchi, Kouichiro; Kurita, Jyoji; Tsuchiya, Takashi Tetrahedron Letters, 2000 , vol. 41, # 21 p. 4143 - 4146
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Citation Number: 33
Abstract
1-Alkynyldiphenylstibines react with acyl chlorides in dichloroethane in the presence of a palladium (0) or (II) catalyst to afford alkynyl ketones by cross-coupling reaction in good to moderate yields. These reactions are highly substituent-selective in that only the alkynyl group could be transferred from the antimony compounds, even in the presence of a large excess of acyl chlorides.
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