Issue 7, 2024

Enantioselective nickel-catalyzed Mizoroki–Heck cyclizations of amide electrophiles

Abstract

Amide cross-couplings that rely on C–N bond activation by transition metal catalysts have emerged as valuable synthetic tools. Despite numerous discoveries in this field, no catalytic asymmetric variants have been disclosed to date. Herein, we demonstrate the first such transformation, which is the Mizoroki–Heck cyclization of amide substrates using asymmetric nickel catalysis. This proof-of-concept study provides an entryway to complex enantioenriched polycyclic scaffolds and advances the field of amide C–N bond activation chemistry.

Graphical abstract: Enantioselective nickel-catalyzed Mizoroki–Heck cyclizations of amide electrophiles

Supplementary files

Article information

Article type
Edge Article
Submitted
30 Oct 2023
Accepted
08 Jan 2024
First published
08 Jan 2024
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2024,15, 2593-2600

Enantioselective nickel-catalyzed Mizoroki–Heck cyclizations of amide electrophiles

A. S. Bulger, D. J. Nasrallah, A. Tena Meza and N. K. Garg, Chem. Sci., 2024, 15, 2593 DOI: 10.1039/D3SC05797F

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