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Progress Towards An Aza-Michael Addition To Ketones, Bowman Potter

Honors Theses

The aza-Michael addition to unsaturated ketones under neutral to mildly basic condition is a difficult transformation due to the inherent unreactivity of ketones toward the addition of weak nucleophiles. This thesis reports on efforts to develop an environmentally friendly, stereoselective and low-cost organo-catalyzed aza-Michael reaction between unsaturated ketones and nitrogen nucleophiles, such as phthalimide, under neutral to mildly basic conditions using the most inexpensive chiral secondary amine catalyst, proline.1 Both proline and the organic base triethylamine were found to be catalytic in the testing platform of cyclohexen-2-one and phthalimide, and another testing platform of 4-hexen-3-one and phthalimide. Likewise, when screened …