Synthesis ( IF 2.6 ) Pub Date : 2018-07-09 , DOI: 10.1055/s-0036-1591587 Victor Anufriev 1 , Dmitry Pelageev 1, 2 , Ksenia Borisova 1
Abstract
A three-step procedure for the synthesis of 1H-benzo[b]xanthene-6,11,12-trione derivatives is described. The procedure involves the halogenation of 12-(3-hydroxy-1,4-naphthoquinon-2-yl)-6H-benzo[b]xanthene-6,11-(12H)-diones, followed by treatment with water under aeration. In this manner, bikaverin, a cytotoxic metabolite isolated from several species of the fungal genera Gibberella, Fusarium, and Mycogone, was synthesised.
A three-step procedure for the synthesis of 1H-benzo[b]xanthene-6,11,12-trione derivatives is described. The procedure involves the halogenation of 12-(3-hydroxy-1,4-naphthoquinon-2-yl)-6H-benzo[b]xanthene-6,11-(12H)-diones, followed by treatment with water under aeration. In this manner, bikaverin, a cytotoxic metabolite isolated from several species of the fungal genera Gibberella, Fusarium, and Mycogone, was synthesised.
中文翻译:
苯并[b]黄嘌呤-6,11,12-三酮的简单路线:比卡维林的合成
摘要
描述了合成1 H-苯并[ b ]氧杂蒽-6,11,12-三酮衍生物的三步程序。该程序包括将12-(3-羟基-1,4-萘醌-2-基)-6 H-苯并[ b ]]吨-6,11-(12 H)-二酮卤化,然后在减压下用水处理通风。以这种方式,合成了比卡韦林,这是一种从真菌属赤霉菌,镰刀菌属和霉菌酮的几种物种中分离出来的细胞毒性代谢产物。
描述了合成1 H-苯并[ b ]氧杂蒽-6,11,12-三酮衍生物的三步程序。该程序包括将12-(3-羟基-1,4-萘醌-2-基)-6 H-苯并[ b ]]吨-6,11-(12 H)-二酮卤化,然后在减压下用水处理通风。以这种方式,合成了比卡韦林,这是一种从真菌属赤霉菌,镰刀菌属和霉菌酮的几种物种中分离出来的细胞毒性代谢产物。