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B(C6F5)3-catalyzed allylation of propargyl acetates with allylsilanes

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ORGANIC LETTERS
卷 6, 期 12, 页码 1999-2001

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AMER CHEMICAL SOC
DOI: 10.1021/ol0494055

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An efficient method for the B(C6F5)(3)-catalyzed allylation of secondary propargylic alcohol derivatives with allylsilanes has been developed. This method allows for the facile synthesis of a variety of 1,5-enynes in good to high yields with a number of functionalities, such as nitro, chloro, ester, and boronic ester, being tolerated under the reaction conditions.

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