960化工网
Anodic oxidation of catechols in the presence of α-oxoketene N,N-acetals with a tetrahydropyrimidine ring: selective α-arylation reaction†
Cheng-Chu Zeng,Da-Wei Ping,Li-Ming Hu,Xiu-Qing Song,Ru-Gang Zhong
Organic & Biomolecular Chemistry Pub Date : 03/24/2010 00:00:00 , DOI:10.1039/C001847C
Abstract

The electrochemical oxidation of catechols leads to the formation of o-benzoquinones. This property has been applied to effectively synthesize α-arylated products of α-oxoketene N,N-acetals with a tetrahydropyrimidine ring.

Graphical abstract: Anodic oxidation of catechols in the presence of α-oxoketene N,N-acetals with a tetrahydropyrimidine ring: selective α-arylation reaction
平台客服
平台客服
平台在线客服