Liddon John T R, James Michael J, Clarke Aimee K, O'Brien Peter, Taylor Richard J K, Unsworth William P
University of York, York, YO24 4PP, UK.
Chemistry. 2016 Jun 20;22(26):8777-80. doi: 10.1002/chem.201601836. Epub 2016 May 19.
Medicinally relevant spirocyclic indolenines, carbazoles and quinolines can each be directly synthesised selectively from common indolyl ynone starting materials by catalyst variation. The high yielding, divergent reactions all proceed by an initial dearomatising spirocyclisation reaction to generate an intermediate vinyl-metal species, which then rearranges selectively by careful choice of catalyst and reaction conditions.
与医学相关的螺环吲哚啉、咔唑和喹啉均可通过改变催化剂,从常见的吲哚基炔酮起始原料直接选择性合成。这些高产率、多向性反应均通过初始的去芳香化螺环化反应进行,生成中间体乙烯基金属物种,然后通过精心选择催化剂和反应条件进行选择性重排。