Issue 17, 2023

Catalyst-controlled stereoselective carbon–heteroatom bond formations by N-heterocyclic carbene (NHC) organocatalysis

Abstract

The development of synthetic strategies towards enantioselective access to carbon–heteroatom bonds by means of catalyst control continues to receive considerable interest in organic chemistry. Over the past decades, N-heterocyclic carbene (NHC) organocatalysis has witnessed extensive exploration for a rapid assembly of asymmetric carbon–heteroatom bonds in a wide range of novel chemical transformations. A diverse set of activation modes and NHC-derived intermediates, such as Breslow intermediates, acyl azoliums, etc., that feature distinct nucleophilicity or electrophilicity have been demonstrated to exhibit substantial potential in the construction of carbon–heteroatom bonds. This review will summarize recent advances in stereoselective carbon–heteroatom bond forming reactions, including C–N, C–O, C–S, C–F, C–P, etc., that were enabled by NHC organocatalysis with a focus on new activation modes and reactive intermediates, aiming to inspire unique insights into the preparation of chiral functional molecules by the use of NHC organocatalysis.

Graphical abstract: Catalyst-controlled stereoselective carbon–heteroatom bond formations by N-heterocyclic carbene (NHC) organocatalysis

Article information

Article type
Review Article
Submitted
06 may 2023
Accepted
26 iyl 2023
First published
27 iyl 2023

Org. Chem. Front., 2023,10, 4437-4458

Catalyst-controlled stereoselective carbon–heteroatom bond formations by N-heterocyclic carbene (NHC) organocatalysis

Y. Wang, Y. Liu, S. Zhao, Y. Long and X. Wu, Org. Chem. Front., 2023, 10, 4437 DOI: 10.1039/D3QO00667K

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