Zhang Lei, Malinakova Helena C
Department of Chemistry, University of Kansas, 1251 Wescoe Hall Drive, Lawrence, KS 66045, USA.
J Org Chem. 2007 Feb 16;72(4):1484-7. doi: 10.1021/jo0621773. Epub 2007 Jan 23.
Copper-catalyzed coupling of imines, dienylstannanes, and acryloyl chlorides followed by a Diels-Alder reaction afforded hexahydro-1H-isoindolones. Diversification of the core via Pd-catalyzed cross-coupling defines a new modular approach to isoindolone combinatorial libraries.
铜催化亚胺、二烯基锡烷和丙烯酰氯的偶联反应,随后进行狄尔斯-阿尔德反应,得到六氢-1H-异吲哚酮。通过钯催化的交叉偶联对核心结构进行多样化修饰,为异吲哚酮组合库定义了一种新的模块化方法。