Cathodic reduction of phenacyl azides

被引:21
作者
Batanero, B [1 ]
Escudero, J [1 ]
Barba, F [1 ]
机构
[1] Univ Alcala de Henares, Dept Organ Chem, Alcala De Henares 28871, Madrid, Spain
关键词
D O I
10.1021/ol990200j
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[GRAPHICS] The electrochemical reduction of phenacyl azides (1a-e) leads to the formation of 2-aroyl-1-4-arylimidazoles (2a-e) (70-80% yield). 1a-e were prepared from phenacyl bromides and sodium azide and were reduced in aprotic DMF-LiClO4 medium at the mercury cathode in a divided cell and under controlled potential.
引用
收藏
页码:1521 / 1522
页数:2
相关论文
共 5 条
[1]  
Baizer M. M., 1991, Organic Electrochemistry, P1265
[2]  
BATANERO B, 1999, IN PRESS SYNTHESIS
[3]   AZIDOCARBONYL COMPOUNDS .1. A NEW SYNTHESIS FOR CERTAIN SUBSTITUTED IMIDAZOLES FROM PHENACYL AZIDES [J].
BOYER, JH ;
STRAW, D .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1952, 74 (18) :4506-4508
[4]  
Lund H, 1967, OSTERREICH CHEM Z, V68, P43
[5]   Concerning glyoxaline. [J].
Pinner, A .
BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1905, 38 :1531-1538