Nishiyama Takashi, Mizuno Shota, Hieda Yuhzo, Choshi Tominari
Faculty of Pharmacy and Pharmaceutical Sciences, Fukuyama University, 1 Sanzo, Gakuen-cho, Fukuyama 729-0292, Japan.
Molecules. 2024 May 18;29(10):2380. doi: 10.3390/molecules29102380.
We present a systematic review of the methods developed for the synthesis of the aromathecin family of compounds (benz[6,7]indolizino[1,2-]quinolin-11(13)-ones) and their derivatives. These methods can be broadly classified into four categories based on the construction of pentacyclic structures: Category 1: by constructing a pyridone moiety (D-ring) on the pyrroloquinoline ring (A/B/C-ring), Category 2: by constructing a pyridine moiety (B-ring) on the pyrroloisoquinolone ring (C/D/E-ring), Category 3: by constructing an indolizidinone moiety (C/D-ring) in a tandem reaction, and Category 4: by constructing a pyrrolidine moiety (C-ring) on the isoquinolone ring (D/E-ring).
我们对用于合成芳香霉素类化合物(苯并[6,7]吲哚并[1,2-]喹啉-11(13)-酮)及其衍生物的方法进行了系统综述。基于五环结构的构建,这些方法可大致分为四类:第1类:通过在吡咯并喹啉环(A/B/C环)上构建吡啶酮部分(D环);第2类:通过在吡咯并异喹啉酮环(C/D/E环)上构建吡啶部分(B环);第3类:通过串联反应构建吲哚嗪酮部分(C/D环);第4类:通过在异喹啉酮环(D/E环)上构建吡咯烷部分(C环)。