作者:Minoru Ishikura、Ayako Hino、Toshikatsu Yaginuma、Isao Agata、Nobuya Katagiri
DOI:10.1016/s0040-4020(99)01016-9
日期:2000.1
The palladium catalyzed tandem cyclization–cross-coupling reaction of indolylborate (2) with vinyl bromide (9) was developed for the preparation of pyrido[4,3-b]carbazole as a key reaction. The cross-coupling reaction of 2a provided hexatriene (10), and then cyclization of 10 to pyrido[4,3-b]carbazole (12) was effected with irradiation or Lewis acid. Using indolylborate (2c) for the cross-coupling
开发了吲哚硼酸酯(2)与乙烯基溴(9)的钯催化串联环化-交叉偶联反应,用于制备吡啶并[4,3- b ]咔唑。2a的交叉偶联反应提供了己三烯(10),然后用辐射或路易斯酸将10环化为吡啶并[4,3- b ]咔唑(12)。使用吲哚硼酸酯(2c)进行交叉偶联反应,通过相似的反应序列获得了玫瑰树碱的新型结构。