Friday, 18 May 2007 - 11:10 AM
210 (Pfahler Hall)
414

Toward the total synthesis of morphine: The asymmetric construction of 5-alkyl, 6-aryl cyclohexenones

David Alan Gerstenhaber and Douglass F. Taber. University of Delaware, Newark, DE

We are developing methods for the asymmetric construction of 5-alkyl,6-aryl cyclohexenones for use in natural product synthesis. We are exploring two approaches: The Fe mediated ring expansion of a vinylcyclopropane, and an organocatalyic Robinson annulation of an aryl ketone with an a,b�unsaturated aldehyde. Our objective is the total synthesis of morphine.


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