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Lewis Base-assisted Arylation of Unsaturated Carbonyls.

Authors :
Lemmerer M
Maulide N
Source :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2023 Nov 24; Vol. 29 (66), pp. e202302490. Date of Electronic Publication: 2023 Oct 24.
Publication Year :
2023

Abstract

The combination of Lewis bases with α,β-unsaturated carbonyls allows the in-situ generation of enolates without the need for strong Brønsted bases. Recently developed synthetic methods employ this approach for arylation followed by elimination of the Lewis base, regenerating the alkene. This strategy has been deployed for formal α- or β-C-H arylation in different contexts, namely (a) transition metal catalysis, (b) rearrangement reactions utilizing hypervalent main group elements and (c) organocatalysis. This concept article provides an overview of the developed strategies, highlighting and contextualizing their features.<br /> (© 2023 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.)

Details

Language :
English
ISSN :
1521-3765
Volume :
29
Issue :
66
Database :
MEDLINE
Journal :
Chemistry (Weinheim an der Bergstrasse, Germany)
Publication Type :
Academic Journal
Accession number :
37647146
Full Text :
https://doi.org/10.1002/chem.202302490