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钴催化的活性烯烃与炔烃的还原偶联反应。

Cobalt-catalyzed reductive coupling of activated alkenes with alkynes.

作者信息

Chang Hong-Tai, Jayanth Thiruvellore Thatai, Wang Chun-Chih, Cheng Chien-Hong

机构信息

Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan.

出版信息

J Am Chem Soc. 2007 Oct 3;129(39):12032-41. doi: 10.1021/ja073604c. Epub 2007 Sep 11.

Abstract

Cobalt complex/Zn systems effectively catalyze the reductive coupling of activated alkenes with alkynes in the presence of water to give substituted alkenes with very high regio- and stereoselectivity in excellent yields. While the intermolecular reaction of acrylates, acrylonitriles, and vinyl sulfones with alkynes takes place in the presence of CoI2(PPh3)2/Zn, the reaction of enones and enals with alkynes requires the use of the CoI2(dppe)/Zn/ZnI2 system. The intramolecular reductive coupling of activated alkenes (enones, enals, acrylates, and acrylonitriles) with alkynes also works efficiently. Further a variety of cyclic lactones and lactams were prepared using this methodology. Possible mechanistic pathways are proposed based on a deuterium-labeling experiment carried out in the presence of D2O.

摘要

钴配合物/锌体系在水存在下能有效催化活性烯烃与炔烃的还原偶联反应,以极高的区域和立体选择性以及优异的产率生成取代烯烃。虽然丙烯酸酯、丙烯腈和乙烯基砜与炔烃的分子间反应在CoI₂(PPh₃)₂/锌存在下发生,但烯酮和烯醛与炔烃的反应需要使用CoI₂(dppe)/锌/碘化锌体系。活性烯烃(烯酮、烯醛、丙烯酸酯和丙烯腈)与炔烃的分子内还原偶联反应也能高效进行。此外,利用该方法制备了多种环状内酯和内酰胺。基于在重水存在下进行的氘标记实验,提出了可能的反应机理途径。

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