Enantioselective Nickel-Catalyzed Denitrogenative Transannulation En Route to N-N Atropisomers

Angew Chem Int Ed Engl. 2024 Jun 21;63(26):e202400441. doi: 10.1002/anie.202400441. Epub 2024 May 24.

Abstract

Nickel-catalyzed transannulation reactions triggered by the extrusion of small gaseous molecules have emerged as a powerful strategy for the efficient construction of heterocyclic compounds. However, their use in asymmetric synthesis remains challenging because of the difficulty in controlling stereo- and regioselectivity. Herein, we report the first nickel-catalyzed asymmetric synthesis of N-N atropisomers by the denitrogenative transannulation of benzotriazones with alkynes. A broad range of N-N atropisomers was obtained with excellent regio- and enantioselectivity under mild conditions. Moreover, density functional theory (DFT) calculations provided insights into the nickel-catalyzed reaction mechanism and enantioselectivity control.

Keywords: N−N atropisomerism; alkynes; asymmetric catalysis; denitrogenative; nickel.