Facile and Convenient Synthesis of N′1,N′3-Dialkyl-N′1,N′3-bis(arylcarbonothioyl)malonohydrazides via Propylphosphonic Anhydride Coupling
作者:Shoujun Chen、Zhiqiang Xia、Jun Jiang、Lijun Sun、Noriaki Tatsuta、Keizo Koya、Junyi Zhang、Gary Bohnert
DOI:10.1055/s-0034-1378664
日期:——
substituted malonic acids using propylphosphonic anhydride (T3P®) under very mild conditions has been developed. A facile and convenient synthetic method for the anticancer agent elesclomol and its analogues, N′1,N′3-dialkyl-N′1,N′3-bis(arylcarbonothioyl)malonohydrazides, by the direct coupling of N-alkyl-N-(substituted)benzothiohydrazides and substituted malonic acids using propylphosphonic anhydride (T3P®)
专用于成业袁教授和有机化学研究所上海(CAS)的李昕戴教授在他们的90个之际个生日 抽象 一种抗癌剂伊利司莫及其类似物,容易且方便的合成方法Ñ ' 1,Ñ ' 3 -二烷基Ñ ' 1,Ñ ' 3双(arylcarbonothioyl)malonohydrazides,通过直接耦合Ñ -烷基- ñ - (取代的)benzothiohydrazides和使用丙基膦酸酐(T3P取代的丙二酸®)已经开发下非常温和的条件。 一种抗癌剂伊利司莫及其类似物,容易且方便的合成方法Ñ ' 1,Ñ ' 3 -二烷基Ñ ' 1,Ñ ' 3双(arylcarbonothioyl)malonohydrazides,通过直接耦合Ñ -烷基- ñ - (取代的)benzothiohydrazides和使用丙基膦酸酐(T3P取代的丙二酸®)已经开发下非常温和的条件。