Issue 17, 2021

An enantioselective aza-Friedel–Crafts reaction of 5-aminoisoxazoles with isatin-derived N-Boc ketimines

Abstract

By employing a chiral phosphoric acid as a catalyst, an enantioselective aza-Friedel–Crafts reaction of 5-aminoisoxazoles with isatin-derived N-Boc ketimines was realized. The reaction provided a wide variety of novel 3-isoxazole 3-amino-oxindoles with good yields (up to 99%) and moderate to good enantioselectivities (up to 99%). The absolute configuration of one product was assigned by X-ray crystal structural analysis and a plausible reaction mechanism was proposed. In addition, a scale-up reaction was performed successfully. Finally, one product was subjected to Suzuki–Miyaura coupling with phenylboronic acid to afford the product in a moderate yield without erosion of the enantioselectivity.

Graphical abstract: An enantioselective aza-Friedel–Crafts reaction of 5-aminoisoxazoles with isatin-derived N-Boc ketimines

Supplementary files

Article information

Article type
Communication
Submitted
26 Feb 2021
Accepted
29 Mar 2021
First published
31 Mar 2021

Org. Biomol. Chem., 2021,19, 3820-3824

An enantioselective aza-Friedel–Crafts reaction of 5-aminoisoxazoles with isatin-derived N-Boc ketimines

H. Liu, Y. Yan, M. Li and X. Zhang, Org. Biomol. Chem., 2021, 19, 3820 DOI: 10.1039/D1OB00374G

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