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靛红与α-烷基-α-重氮酯的催化不对称环扩张反应:功能化 2-喹诺酮衍生物的高效合成。

A catalytic asymmetric ring-expansion reaction of isatins and α-alkyl-α-diazoesters: highly efficient synthesis of functionalized 2-quinolone derivatives.

机构信息

Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, China.

出版信息

Angew Chem Int Ed Engl. 2012 Aug 20;51(34):8644-7. doi: 10.1002/anie.201204594. Epub 2012 Jul 23.

Abstract

Asymmetric expansion: A catalytic asymmetric ring-expansion reaction of the title compounds occurs in the presence of a Sc(OTf)(3) catalyst bearing an N,N'-dioxide-based ligand. Highly functionalized 2-quinolone derivatives containing a chiral C4-quaternary stereocenter were obtained in high yields and high levels of selectivity under mild reaction conditions (see scheme; Tf=trifluoromethanesulfonyl).

摘要

不对称扩张

标题化合物在负载基于 N,N'-二氧杂环戊烷的配体的 Sc(OTf)(3)催化剂存在下发生催化不对称环扩张反应。在温和的反应条件下,以高产率和高立体选择性得到了含有手性 C4-季碳立体中心的高官能化 2-喹诺酮衍生物(参见方案;Tf=三氟甲磺酸基)。

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