From: Joerg K. W. <we...@in...> - 2004-03-22 14:58:42
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Hi, > That's why I posted the question to the cdk-devel list too, to see > whether others have any idea. > To be honest, I'm was not sure about the aromaticity of quinone, which > is quite embarrising :-) Me, too :-) I've found: Since the dienophile (quinone) has two activated double bonds, a second cycloaddition reaction is possible, provided sufficient diene is supplied. http://www.cem.msu.edu/~reusch/VirtualText/pericycl.htm Kind regards, Joerg -- Dipl. Chem. Joerg K. Wegner Center of Bioinformatics Tuebingen (ZBIT) Department of Computer Architecture Univ. Tuebingen, Sand 1, D-72076 Tuebingen, Germany Phone: (+49/0) 7071 29 78970 Fax: (+49/0) 7071 29 5091 E-Mail: mailto:we...@in... WWW: http://www-ra.informatik.uni-tuebingen.de -- Never mistake motion for action. (E. Hemingway) Never mistake action for meaningful action. (Hugo Kubinyi,2004) |