Chiral Brønsted Acid-Catalyzed Formal α-Vinylation of Cyclopentanones for the Enantioselective Construction of Quaternary Carbon Centers

Volume: 9, Issue: 8, Pages: 6846 - 6850
Published: Jun 28, 2019
Abstract
An enantioselective formal α-vinylation of ketones for the construction of an all-carbon quaternary center was established using the vinylogous Wagner–Meerwein shift through the activation of the leaving group by a chiral phosphoramide as the chiral Brønsted acid catalyst. The present reaction afforded enantioenriched all-carbon quaternary α-vinyl ketones in high yields with high enantioselectivities in most cases. Experimental elucidation of...
Paper Details
Title
Chiral Brønsted Acid-Catalyzed Formal α-Vinylation of Cyclopentanones for the Enantioselective Construction of Quaternary Carbon Centers
Published Date
Jun 28, 2019
Volume
9
Issue
8
Pages
6846 - 6850
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