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首页> 外文期刊>Chemical Communications >Lithium acetylides as alkynylating reagents for the enantioselective alkynylation of ketones catalyzed by lithium binaphtholate
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Lithium acetylides as alkynylating reagents for the enantioselective alkynylation of ketones catalyzed by lithium binaphtholate

机译:乙炔锂作为炔基化试剂,用于对萘二甲酸锂催化的酮的对映选择性炔基化

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摘要

Chiral lithium binaphtholate effectively catalyzed the enantioselective alkynylation of ketones using lithium acetylide as an alkynylating agent. This is the first example of the catalytic enantioselective addition of lithium acetylide to carbonyl compounds without the aid of other metal sources.
机译:使用乙炔化锂作为炔基化剂,手性联萘甲酸锂有效地催化了酮的对映选择性炔基化。这是在不借助其他金属源的情况下将乙炔化锂催化对映选择性加成至羰基化合物的第一个例子。

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  • 来源
    《Chemical Communications》 |2011年第19期|p.5614-5616|共3页
  • 作者单位

    Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto, Japan;

    Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto, Japan;

    Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto, Japan;

    Priority Organization for Innovation and Excellence, Kumamoto University, 5-1 Oe-honmachi, Kumamoto, Japan;

    Graduate School of Pharmaceutical Sciences, Kumamoto University, 5-1 Oe-honmachi, Kumamoto, Japan;

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