Vilsmeier Reaction of Enaminones: Efficient Synthesis of Halogenated Pyridin-2(1H)-ones


Autoria(s): Zhang R; Zhang DY; Guo YL; Zhou GY; Jiang ZJ; Dong DW
Data(s)

2008

Resumo

A facile and efficient one-pot synthesis of halogenated pyridin-2(1H)-ones from a series of readily available enaminones under Vilsmeier conditions is described, and a mechanism involving sequential halogenation, formylation, and intramolecular nucleophilic cyclization is proposed.

Identificador

http://ir.ciac.jl.cn/handle/322003/10261

http://www.irgrid.ac.cn/handle/1471x/147366

Idioma(s)

英语

Fonte

Zhang R;Zhang DY;Guo YL;Zhou GY;Jiang ZJ;Dong DW.Vilsmeier Reaction of Enaminones: Efficient Synthesis of Halogenated Pyridin-2(1H)-ones,JOURNAL OF ORGANIC CHEMISTRY,2008,73(23):9504-9507

Palavras-Chave #HIGHLY SUBSTITUTED PYRIDIN-2(1H)-ONES #ONE-POT SYNTHESIS #FACILE SYNTHESIS #HAACK REACTIONS #ASYMMETRIC HYDROGENATION #ACRYLATE DERIVATIVES #CARBONYL-COMPOUNDS #ACID-DERIVATIVES #PYRIDINE RINGS #INHIBITORS
Tipo

期刊论文