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使用多任务钯催化剂通过连续的Heck还原-环化(HRC)反应制备2-喹诺酮类化合物。

Preparation of 2-quinolones by sequential Heck reduction-cyclization (HRC) reactions by using a multitask palladium catalyst.

作者信息

Felpin François-Xavier, Coste Jérôme, Zakri Cécile, Fouquet Eric

机构信息

Université de Bordeaux, CNRS, Institut des Sciences Moléculaires, 351 Cours de la Libération, 33405 Talence, France.

出版信息

Chemistry. 2009 Jul 20;15(29):7238-45. doi: 10.1002/chem.200900583.

Abstract

One-pot sequential Heck reduction-cyclization (HRC) reactions leading to the synthesis of substituted 2-quinolones have been developed by using a heterogeneous or mixed homogeneous/heterogeneous multitask palladium catalyst with charcoal as a support. The whole sequence occurs under very mild conditions without the need for additives (ligand or base) by taking advantage of the high reactivity of aryldiazonium salts as "super electrophiles". Recycling experiments showed that the reused heterogeneous Pd(0)/C catalyst was not able to promote another HRC sequence but was, however, still highly active for hydrogenation, hydrodehalogenation, as well as hydrogenolysis reactions.

摘要

通过使用以木炭为载体的多相或均相/多相混合多任务钯催化剂,开发了一锅法连续Heck还原环化(HRC)反应,用于合成取代的2-喹诺酮。利用芳基重氮盐作为“超级亲电试剂”的高反应活性,整个反应序列在非常温和的条件下进行,无需添加剂(配体或碱)。循环实验表明,重复使用的多相Pd(0)/C催化剂不能促进另一个HRC反应序列,但对氢化、加氢脱卤以及氢解反应仍具有高活性。

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