960化工网
Scandium triflate-catalyzed selective ring opening and rearrangement reaction of spiro-epoxyoxindole and carbonyl compounds†
Haohua Jie,Jian Li
RSC Advances Pub Date : 10/17/2016 00:00:00 , DOI:10.1039/C6RA21264F
Abstract

Scandium triflate-catalyzed reactions between spiro-epoxyoxindole and carbonyl compounds have been disclosed. The reaction with ketones can be used to synthesize spiro[[1,3]dioxolane-4,3′-indolin] species. Furthermore, an unprecedented rearrangement takes place to yield alkylidene oxindole when aromatic aldehydes are used as carbonyl components.

Graphical abstract: Scandium triflate-catalyzed selective ring opening and rearrangement reaction of spiro-epoxyoxindole and carbonyl compounds
平台客服
平台客服
平台在线客服