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Rhodium(III)-catalyzed intramolecular annulation through C–H activation: concise synthesis of rosettacin and oxypalmatime
Chemical Communications ( IF 4.9 ) Pub Date : 2017-09-21 00:00:00 , DOI: 10.1039/c7cc06860c
Liangliang Song 1, 2, 3 , Guilong Tian 1, 2, 3 , Yi He 1, 2, 3 , Erik V. Van der Eycken 1, 2, 3, 4, 5
Affiliation  

A flexible and efficient rhodium(III)-catalyzed intramolecular annulation of benzamides bearing tethered alkynes for the synthesis of indolizinones and quinolizinones is reported. This reaction shows a broad substrate scope and excellent functional-group tolerance, including different kinds of heterocyclic substrates, such as furan, thiophene, pyrrole, benzofuran, benzothiophene, indole and isonicotinamide substrates. This method also provides a practical and efficient approach for the synthesis of rosettacin and oxypalmatime.

中文翻译:

铑(III)通过C–H活化催化分子内环化:罗塞他汀和羟帕马汀的简明合成

报道了一种柔性且有效的铑(III)催化的带有链状炔烃的苯甲酰胺的分子内环化反应,用于合成吲哚嗪酮和喹啉酮。该反应显示出较宽的底物范围和优异的官能团耐受性,包括不同种类的杂环底物,例如呋喃,噻吩,吡咯,苯并呋喃,苯并噻吩,吲哚和异烟酰胺底物。该方法还提供了一种合成罗塞他汀和羟帕马汀的实用而有效的方法。
更新日期:2017-11-16
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