A Highly Diastereoselective Tertiary Amine‐Catalyzed Cascade Michael—Michael—Henry Reaction Between Nitromethane, Activated Alkenes and α,β‐Unsaturated Carbonyl Compounds.
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A new tertiary amine-catalyzed cascade Michael-Michael-Henry reaction between nitromethane, a doubly activated alkene and an α,β-unsaturated carbonyl compound is described, which provides a convenient and efficient synthesis for densely functionalized cyclohexanes and some bicyclic compounds in moderate to excellent yields with high diastereoselectivity.