Department of Chemistry, Indian Institute of Technology Madras , Chennai 600 036, Tamil Nadu, India.
Org Lett. 2017 Apr 7;19(7):1694-1697. doi: 10.1021/acs.orglett.7b00482. Epub 2017 Mar 13.
An unprecedented Henry reaction of in situ generated nitrosocarbonyl intermediates and concomitant denitration cascade has been developed. The reaction is catalyzed by organic base at room temperature offering α-ketoamides, a demanding scaffold for drug discovery, in high yields. An alteration of substitution pattern also produced α-keto oximes, a high-value synthon. The protocol features operational simplicity and broad substrate scope.
发展了一种前所未有的原位生成亚硝酰基中间体的 Henry 反应和伴随的脱硝级联反应。该反应在室温下由有机碱催化,以高产率提供α-酮酰胺,这是药物发现中要求苛刻的支架。取代模式的改变也产生了高价值的合成子α-酮肟。该方案具有操作简单和广泛的底物范围的特点。