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Catalytic Propargylic Substitution Reactions

机译:催化炔丙基取代反应

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In sharp contrast to the well-established transition metal-catalyzed allylic substitution reactions, the study of the corresponding propargylic substitution reactions has been quite limited for constructing carbon-carbon and carbon-heteroa-tom bonds at the propargylic position, However, during the last decade, general and useful catalytic reactions have been developed extensively. In this Review, we summarize recent advances in catalytic propargylic substitution reactions of propargylic alcohols and their derivatives with heteroatom- and carbon-centered nucleophiles. In addition to a variety of transition metals, such as Ru, Re, Rh, Ir, Ni, Pd, Pt, and Cu, which form organometallic species as intermediates, several Lewis acids and Bronsted acids are also applicable as catalysts in these reactions. The reaction mechanism and the scope of nucleophiles that can be used depend on the nature of the catalysts. Some examples of enantioselective substitution reactions at the propargylic position are also described.
机译:与公认的过渡金属催化的烯丙基取代反应形成鲜明对比的是,对于在炔丙基位置上构建碳-碳和碳-杂-原子键,相应的炔丙基取代反应的研究非常有限,但是,在最后十年来,已经广泛地开发了通用和有用的催化反应。在这篇综述中,我们总结了炔丙醇及其衍生物与杂原子和以碳为中心的亲核试剂催化丙炔取代反应的最新进展。除了形成有机金属物质作为中间体的各种过渡金属(如Ru,Re,Rh,Ir,Ni,Pd,Pt和Cu)外,几种路易斯酸和布朗斯台德酸也可用作这些反应的催化剂。可以使用的亲核试剂的反应机理和范围取决于催化剂的性质。还描述了在炔丙基位置的对映选择性取代反应的一些实例。

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