Asymmetric organocatalytic double 1,6-addition: rapid access to chiral chromans with molecular complexity
Literature Information
Publication Date
2020-04-28
DOI
10.1039/D0QO00354A
Impact Factor
5.281
Authors
Sourav Roy, Suman Pradhan, Krishan Kumar, Indranil Chatterjee
View Original
Abstract
An organocatalytic cascade vinylogous double 1,6-addition strategy for the synthesis of chiral chroman derivatives is reported. The cascade reaction follows oxa-Michael/1,6-addition reactions between ortho-hydroxyphenyl-substituted para-quinone methides and 2,4-dienal derivatives to deliver chroman derivatives with excellent yields (up to 96%) and stereoselectivities (up to >20 : 1 dr, >99% ee). The chiral secondary amine-based Jørgensen–Hayashi organocatalysts are shown to catalyze the transformation of unbiased 2,4-dienals under mild reaction conditions with exclusive δ-site selectivity and high control over enantioselectivity at a remote position. The synthetic transformations of the products ensure molecular complexity with a great level of enantiocontrol.
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Organic Chemistry Frontiers
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