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Palladium-Catalyzed [5+1] Annulation of 2-(1-Arylvinyl) Anilines and α-Diazocarbonyl Compounds toward Multi-functionalized Quinolines
Advanced Synthesis & Catalysis ( IF 5.4 ) Pub Date : 2017-09-14 06:45:38 , DOI: 10.1002/adsc.201701069
Jiawei Zhu 1 , Weiming Hu 1 , Song Sun 1 , Jin-Tao Yu 1 , Jiang Cheng 1
Affiliation  

A palladium-catalyzed [5+1] annulation of 2-(1-arylvinyl) anilines and α-diazocarbonyl compounds has been developed, affording a series of multi-functionalized quinolines in moderate to good yields. This procedure proceeded with the sequential insertion of N−H bond to the palladium carbene, intramolecular Heck reaction and decarboxylation steps. In this reaction, alkyl 2-diazophenylacetates served as C1 building block, which represents a key compliment to diazo chemistry.

中文翻译:

钯催化2-(1-芳基乙烯基)苯胺和α-重氮羰基化合物对多官能喹啉的[5 + 1]环化

已经开发了钯催化的2-(1-芳基乙烯基)苯胺和α-重氮羰基化合物的[5 + 1]环,以中等到良好的产率提供了一系列多官能化的喹啉。该程序通过将NH键顺序插入钯卡宾,分子内Heck反应和脱羧步骤进行。在该反应中,2-重氮苯基乙酸烷基酯用作C1结构单元,代表了对重氮化学的关键补充。
更新日期:2017-09-14
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