Fused 6,6,5-ring systems Q 1070 Functionalization of Csp 3 -H Bond-Sc(OTf)3-Catalyzed Domino 1,5-Hydride Shift/Cyclization/Friedel-Crafts Acylation Reaction of Benzylidene Meldrum's Acids. -Mild thermolysis of title compounds bearing a tethered electron-rich phenethyl group in the presence of Sc(O-Tf)3 results in a [1.5]-hydride shift/cyclization reaction to give spiro Meldrum's acid intermediates. On further heating at 100°C, they undergo intramolecular Friedel-Crafts cyclization to yield the desired tetracyclic skeleton of tetrahydrobenzo[b]fluoren-11-ones. -(MAHONEY, S. J.; MOON, D. T.; HOLLINGER, J.; FILLION*, E.; Tetrahedron Lett. 50 (2009) 33, 4706-4709; Dep. Chem., Univ. Waterloo, Waterloo, Ont. N2L 3G1, Can.; Eng.) -Mais 48-105
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.