Preparation of 2-Quinolones by Sequential Heck Reduction-Cyclization (HRC) Reactions by Using a Multitask Palladium Catalyst

被引:88
作者
Felpin, Francois-Xavier [1 ]
Coste, Jerome [1 ]
Zakri, Cecile [2 ]
Fouquet, Eric [1 ]
机构
[1] Univ Bordeaux, CNRS, Inst Mol Sci, 351 Cours Liberat, F-33405 Talence, France
[2] Univ Bordeaux, CNRS, Ctr Rech Paul Pascal, F-33600 Pessac, France
关键词
diazo compounds; Heck reaction; one-pot reactions; palladium; sustainable chemistry; ONE-POT SYNTHESIS; ARENEDIAZONIUM TETRAFLUOROBORATE SALTS; CROSS-COUPLING REACTIONS; BAYLIS-HILLMAN ADDUCTS; ALLYLIC ALKYLATION; ORGANIC-SYNTHESIS; CASCADE REACTIONS; DOMINO REACTIONS; PALLADIUM(0)-CATALYZED ARYLATION; HETEROGENEOUS CATALYST;
D O I
10.1002/chem.200900583
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:7238 / 7245
页数:8
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