REDUCTIVE CYCLISATION OF SOME DERIVATIVES OF METHYL 0-NITROPHENYL-PYRUVATE AND OTHER KETO-ESTERS BY CATALYSED SODIUM BOROHYDRIDE

被引:9
作者
COUTTS, RT
MUKHERJE.G
ABRAMOVI.RA
BREWSTER, MA
机构
[1] Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, Alta.
[2] Department of Chemistry, University of Alabama, University, AL
[3] College of Pharmacy, University of Saskatchewan, Saskatoon, Sask.
来源
JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC | 1969年 / 16期
关键词
D O I
10.1039/j39690002207
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
3-Amino-1-hydroxyquinolin-2(1H)-one (Va) is one of the products when the oxime of methyl o-nitrophenylpyruvate is reduced with sodium borohydride and palladium-charcoal. The claim that the same quinolone is one of the products of the catalytic hydrogenation of ethyl o-nitrophenylpyruvate oxime is shown to be erroneous. Reduction of the oximino-, benzylidene, and other derivatives of selected keto-esters with sodium borohydride and palladium-charcoal is described.
引用
收藏
页码:2207 / &
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