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首页> 外文期刊>The Journal of Organic Chemistry >Lewis Acid Catalyzed Friedel-Crafts Alkylation of Alkenes with Trifluoropyruvates
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Lewis Acid Catalyzed Friedel-Crafts Alkylation of Alkenes with Trifluoropyruvates

机译:刘易斯酸与三氟丙酮酸催化烯烃的弗里德-克拉夫茨烷基化

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摘要

A Friedel-Crafts alkylation reaction of styrenes with trifluoropyruvates has been developed, which delivered allylic alcohols in excellent yields (up to 98%) using the Ni(ClO4)(2)center dot 6H(2)O/bipyridine complex as a catalyst. The asymmetric reaction was catalyzed by the chiral Cu(OTf)(2)/bisoxazoline complex to afford the corresponding chiral allylic alcohols bearing trifluoromethylated quaternary stereogenic centers in moderate enantioselectivities (up to 75% ee).
机译:已开发出苯乙烯与三氟丙酮酸盐的弗里德-克来福特烷基化反应,使用Ni(ClO4)(2)中心点6H(2)O /联吡啶配合物作为催化剂,可以以极高的收率(高达98%)提供烯丙醇。手性Cu(OTf)(2)/双恶唑啉配合物催化不对称反应,得到相应的手性烯丙醇,其具有中等对映选择性(最高75%ee)的三氟甲基化季立体中心。

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