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Enantioselective Assembly of Substituted Dihydropyrones Via Organocatalytic Reaction in Water Media

Overview
Journal Org Lett
Specialties Biochemistry
Chemistry
Date 2008 May 15
PMID 18476713
Citations 4
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Abstract

The diarylprolinol ether/HOAc-catalyzed cascade Michael addition and cyclization of aldehydes and alpha-keto-alpha,beta-unsaturated esters proceeds smoothly in water to afford cyclic hemiacetals, which are oxidized to furnish highly functionalized 3,4,5,6-tetrasubstituted dihydropyrones with excellent enantioselectivities.

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