化学
甲酰化
甲酸
芳基
咪唑
催化作用
腈
药物化学
有机化学
烷基
作者
Sukhen Karmakar,Sundar Nadhagopal,Zulelal Dolas,Arundutt Silamkoti,Anuradha Gupta,Arvind Mathur
出处
期刊:Synlett
[Thieme Medical Publishers (Germany)]
日期:2023-03-06
卷期号:34 (15): 1809-1813
被引量:1
摘要
Abstract A carbonyldiimidazole (CDI)-promoted generation of CO from formic acid has been exploited in a reductive formylation of aryl iodides in the presence of tris(dibenzylideneacetone)dipalladium. The reaction conditions are mild with a broad functional-group tolerance that includes keto, bromo, nitrile, ester, and nitro groups. In the reaction pathway, CDI reacts with formic acid to generate a formyl imidazole that ultimately produces the CO needed for the formylation process on the activated arylpalladium complex.
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