Issue 39, 2020

Enantioselective vinylogous aldol/lactonization cascade reaction between β,γ-unsaturated amides and trifluoromethyl ketones: facile access to chiral trifluoromethyl dihydropyranones

Abstract

An efficient asymmetric vinylogous aldol/lactonization cascade reaction between β,γ-unsaturated amides and trifluoromethyl ketones has been developed. Using a chiral cyclohexanediamine-based tertiary amine-thiourea catalyst, optically active trifluoromethyl dihydropyranones have been constructed in moderate-to-excellent yields (up to 99%) with excellent stereoselectivities (96–> 99.5% ee).

Graphical abstract: Enantioselective vinylogous aldol/lactonization cascade reaction between β,γ-unsaturated amides and trifluoromethyl ketones: facile access to chiral trifluoromethyl dihydropyranones

Supplementary files

Article information

Article type
Communication
Submitted
24 Aug 2020
Accepted
21 Sep 2020
First published
22 Sep 2020

Org. Biomol. Chem., 2020,18, 7848-7851

Enantioselective vinylogous aldol/lactonization cascade reaction between β,γ-unsaturated amides and trifluoromethyl ketones: facile access to chiral trifluoromethyl dihydropyranones

J. Fu, Z. Zhang, X. Zhou, C. Fu, F. Sha and X. Wu, Org. Biomol. Chem., 2020, 18, 7848 DOI: 10.1039/D0OB01746A

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