O'Connor N, Mornet R, Matringe M, Clair D, Scalla R, Fujimoto T T, Swithenbank C
Laboratoire de Chimie Organique Fondamentale et Appliquée, Faculté des Sciences, Angers, France.
Bioorg Med Chem. 1994 May;2(5):339-42. doi: 10.1016/s0968-0896(00)82190-2.
A diazoketone 3 has been synthesized in two steps from acifluorfen 1, a diphenyl ether herbicide. Like the parent compound 1, the diazoketone 3 is toxic to plant cells and inhibits protoporphyrinogen oxidase, the molecular target of diphenyl ether herbicides. On photolysis of 3 in methanol, the generated carbene mainly undergoes the Wolff rearrangement to a ketene which further adds methanol, but many other products are observed. A tritiated derivative of 3 has been prepared which is suitable for photoaffinity labeling experiments.
已通过两步反应从二苯醚除草剂三氟羧草醚1合成了重氮酮3。与母体化合物1一样,重氮酮3对植物细胞有毒,并抑制原卟啉原氧化酶,这是二苯醚除草剂的分子靶点。在甲醇中对3进行光解时,生成的卡宾主要发生沃尔夫重排生成烯酮,烯酮进一步与甲醇加成,但还观察到许多其他产物。已制备了3的氚代衍生物,适用于光亲和标记实验。