Issue 11, 2024

Enantioselective synthesis of spiro-N,O-ketals via iridium and Brønsted acid co-catalyzed asymmetric formal [4+2] cycloaddition

Abstract

We present an iridium and Brønsted acid co-catalyzed enantioselective formal [4+2] cycloaddition reaction of cyclic enamides with 2-(1-hydroxyallyl)phenols. This method yields a wide range of N-unsubstituted spiro-N,O-ketals, with good efficiency (up to 94%) and excellent enantioselectivities (most >95% ee). The protocol features easy scale-up and facile product derivatization.

Graphical abstract: Enantioselective synthesis of spiro-N,O-ketals via iridium and Brønsted acid co-catalyzed asymmetric formal [4+2] cycloaddition

Supplementary files

Article information

Article type
Communication
Submitted
04 Dec 2023
Accepted
03 Jan 2024
First published
03 Jan 2024

Chem. Commun., 2024,60, 1448-1451

Enantioselective synthesis of spiro-N,O-ketals via iridium and Brønsted acid co-catalyzed asymmetric formal [4+2] cycloaddition

X. Xie, X. Li and P. Liu, Chem. Commun., 2024, 60, 1448 DOI: 10.1039/D3CC05923E

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