Diels−Alder Reactions of Quinol Lactones: A Change of Regioselectivity with Stannic Chloride CatalysisThe Journal of Organic Chemistry
Publication VersionPublished Version
Lewis acid-mediated Diels−Alder reactions of quinol lactone 2 gave regioselectivity opposite to that of the uncatalyzed reaction. Compound 12 is proposed as the reactive intermediate generated by the reaction of 2 with stannic chloride.
Copyright OwnerAmerican Chemical Society
Citation InformationGeorge A. Kraus and Wenge Cui. "Diels−Alder Reactions of Quinol Lactones: A Change of Regioselectivity with Stannic Chloride Catalysis" The Journal of Organic Chemistry Vol. 67 Iss. 26 (2002) p. 9475 - 9476
Available at: http://works.bepress.com/george_kraus/137/