Litcius/Paper detail

Organocatalytic Asymmetric Addition of Aromatic α-Cyanoketones to <i>o</i>-Quinone Methides: Synthesis of 3,4-Dihydrocoumarins and Tetrasubstituted Chromans

Chandan Gharui, Chandrakanta Parida, Subhas Chandra Pan

2021The Journal of Organic Chemistry14 citationsDOI

Abstract

The first organocatalytic asymmetric addition of aromatic α-cyanoketones to in situ-generated o-quinone methides has been developed. The products 3,4-dihydrocoumarin and tetrasubstituted chroman were obtained via addition of aromatic α-cyanoketones to in situ-generated o-quinone methides followed by treatment with 0.7 N HCl. With 10 mol % catalyst, the desired products were obtained in high enantio- and diastereoselectivities.

Topics & Concepts

ChemistryQuinoneCatalysisIn situOrganocatalysisOrganic chemistryEnantioselective synthesisSynthesis of Indole DerivativesAxial and Atropisomeric Chirality SynthesisMulticomponent Synthesis of Heterocycles
Organocatalytic Asymmetric Addition of Aromatic α-Cyanoketones to <i>o</i>-Quinone Methides: Synthesis of 3,4-Dihydrocoumarins and Tetrasubstituted Chromans | Litcius