Vomero S, Chimenti F, Giuliano R, Artico M
Farmaco Sci. 1976 Sep;31(9):681-90.
The synthesis of pyrrolo[1,2-a]quinoline derivatives from 1-arylpyrroles bearing an acetic acid or acetonitrile moiety on the benzene or pyrrole nucleus is described. Pyrrolo [1,2-a]quinoline derivatives have some pharmaceutical interest as cyclic analogues of 9H-pyrrolo[1,2-a]indole and 5H-pyrrolo[2,1-c] [1,4]-benzodiazepine, the basic structures of the antitumor antibiotics mitomycin C, anthramycin and tomaymycin.
描述了从在苯环或吡咯环上带有乙酸或乙腈部分的1-芳基吡咯合成吡咯并[1,2-a]喹啉衍生物。吡咯并[1,2-a]喹啉衍生物作为9H-吡咯并[1,2-a]吲哚和5H-吡咯并[2,1-c][1,4]-苯并二氮杂卓的环状类似物具有一定的药学意义,它们分别是抗肿瘤抗生素丝裂霉素C、安曲霉素和托马霉素的基本结构。