首页> 外文会议>European Symposium on Organic Chemistry >1,1,1,3,3,3-Hexafluoroisopropanol as a Media of Choice for Electrophilic Alkylation of π-donors in the Absence of Lewis Acids(Abstracts)
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1,1,1,3,3,3-Hexafluoroisopropanol as a Media of Choice for Electrophilic Alkylation of π-donors in the Absence of Lewis Acids(Abstracts)

机译:1,1,1,3,3,3,3-六氟异丙醇作为π-供体在没有路易斯酸的π-供体的选择培养基(摘要)

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摘要

Owing to the unique properties (high ionizing power and low nucleophilicity) 1,1,1,3,3,3-hexafluoroisopropanol (HFIP) was shown to he an almost ideal solvent for performing a number of transformations such as selective oxidation, oxirane ring opening and aza-Diels-Alder reactions . Here we wish to present the data attesting to the usefulness of HFIP as a specific media securing an opportunity to carry out the electrophilic alkylations of various π-donors under remarkably mild conditions in the absence of any Lewis acids.
机译:由于独特的性质(高电离功率和低亲核性),示出了1,1,3,3,3,3-六氟异丙醇(HFIP),其几乎理想的溶剂用于进行多种转化,例如选择性氧化,氧化乙烷环开口和AZA-Diels-Alder反应。在这里,我们希望展示证明HFIP的有用性的数据,作为特定媒体,确保在不存在任何路易斯酸的情况下在显着的温和条件下在显着温和的条件下在不存在显着温和的条件下在不存在的情况下进行电泳烷基化的机会。

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