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Catalytic Asymmetric Multicomponent Reductive/Alkylative Aldol Reactions with Allenic Esters and Unactivated Ketones(Abstracts)

机译:催化不对称的多组分还原/烷基化醛醇与烯丙酯和未活化的酮(摘要)

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摘要

Development of asymmetric reactions that assemble three or more reagents in one-pot under the promotion and streo-control by an asymmetric catalyst (catalytic asymmetric multicomponent reaction: CAMCR) is great challenge today. Specifically, CAMCR that can construct chiral tetrasubstituted carbons has just begun to be explored. These reactions can rapidly increase the molecular complexity from relatively simple reactants, and produce structurally diverse array of chiral building blocks containing tetrasubsituted carbons, which are inaccessible by known reactions. We will present a copper-catalyzed asymmetric multicomponent reductive/alkylative aldol reaction that assembles ketones, allenic esters, and pinacolborane/dialkylzincs.
机译:通过不对称催化剂(催化不对称多组分反应:CAMCR)在促进和促促促进和四孔中组装三个或更多种试剂的不对称反应的发展,这是今天的挑战。具体而言,可以构建手性四氢碳的CAMCR刚刚开始探索。这些反应可以迅速增加来自相对简单的反应物的分子复杂性,并在结构上产生含有四氢碳的细胞构建块阵列,其难以通过已知反应可接近的。我们将呈现一种铜催化的不对称多组分还原/烷基化醛醇反应,其组装酮,硫代酯和PINACOLBOLANE /二烷基锌。

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