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铜催化的深入研究:芳基/吲哚基硼酸Suzuki-Miyaura 交叉偶联反应中形成的纳米 CuO。

Insight into Copper Catalysis: In Situ Formed Nano CuO in Suzuki-Miyaura Cross-Coupling of Aryl/Indolyl Boronates.

机构信息

School of Chemistry, University of Hyderabad , Hyderabad - 500046, India.

出版信息

Org Lett. 2017 Aug 4;19(15):3974-3977. doi: 10.1021/acs.orglett.7b01669. Epub 2017 Jul 19.

Abstract

A ligand-free copper catalyzed Suzuki-Miyaura coupling of 3,5-diiodopyridine with aryl and indole boronates has been explored in good to excellent yields. In situ generation of nano-CuO from CuCl under the reaction conditions has been discovered for the first time. The generality of the reaction was further demonstrated by the arylation of 5-iodopyrimidine, iodopyridines, iodobenzenes, and diiodobenzenes and resulted in good to moderate yields. Moreover, bisindole alkaloid Scalaridine A has been successfully synthesized in 60% overall yield.

摘要

一种无配体的铜催化 3,5-二碘吡啶与芳基和吲哚硼酸酯的铃木-宫浦偶联反应在良好到优异的产率下得到了探索。在反应条件下,首次发现从 CuCl 原位生成纳米 CuO。该反应的通用性通过 5-碘嘧啶、碘吡啶、碘苯和二碘苯的芳基化进一步得到证明,得到了良好到中等的产率。此外,双吲哚生物碱 Scalaridine A 也以 60%的总收率成功合成。

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