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HFIP 催化的二氟烯基硅烷与苄醇和烯丙醇的直接去羟二氟烷基化反应。

HFIP-catalyzed direct dehydroxydifluoroalkylation of benzylic and allylic alcohols with difluoroenoxysilanes.

机构信息

Advanced Research Institute and Department of Chemistry, Taizhou University, 1139 Shifu Avenue, Taizhou 318000, P. R. China.

Department of Chemistry, Zhejiang University, Hangzhou 310058, P. R. China.

出版信息

Chem Commun (Camb). 2021 Feb 1;57(8):1050-1053. doi: 10.1039/d0cc06980a.

Abstract

Hexafluoroisopropanol (HFIP)-catalyzed direct dehydroxydifluoroalkylation of benzylic and allylic alcohols with difluoroenoxysilanes is developed. This procedure enables the synthesis of a broad range of α,α-difluoroketones, a class of highly valuable intermediates and building blocks in medicinal and organic chemistry. Here, we have demonstrated for the first time that HFIP could act as a powerful catalyst for fluorinated carbon-carbon bond formation. The application of this protocol in late-stage dehydroxydifluoroalkylation of potentially bioactive drugs and natural products has also been carried out.

摘要

六氟异丙醇 (HFIP) 催化的二氟烯氧基硅烷与苄基和烯丙基醇的直接脱氢二氟烷基化反应被开发出来。该方法可用于合成广泛的α,α-二氟酮,这是一类在药物和有机化学中具有重要价值的中间体和构建块。在这里,我们首次证明 HFIP 可以作为氟化碳-碳键形成的有力催化剂。该方法还被应用于具有潜在生物活性的药物和天然产物的后期脱氢二氟烷基化反应。

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