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Chiral Amine-Catalyzed Asymmetric Conjugate Addition of Aldehydes to α-Phenylselenoenones as Z-Allylating Agents

机译:作为Z-烯丙基化剂的手性胺催化的不对称缀合物加入α-苯基硒烯酮的醛

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摘要

The asymmetric alkylation of aldehydes and ketones with chiral amine organocatalysts remains a challenge due to the undesired N-alkylation and deactivation of such amines. On the other hand, optically enriched E-allylation products can be prepared through the chiral aminecatalyzed reactions.1 However, the enantioselective introduction of Z-allyl groups has not been developed to date.
机译:由于不希望的N-烷基化和这种胺失活,具有手性胺有机催化剂的醛和酮的不对称烷基化仍然是挑战。另一方面,光学富集的e-烯丙基化产品可以通过手性氨因盐反应制备。然而,迄今为止尚未开发Z-烯丙基组的对致映选择性引入。

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