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Selectivity in Rh-catalysis with gem -difluorinated cyclopropanes.

Authors :
Zeng Y
Jiang ZT
Xia Y
Source :
Chemical communications (Cambridge, England) [Chem Commun (Camb)] 2024 Apr 02; Vol. 60 (28), pp. 3764-3773. Date of Electronic Publication: 2024 Apr 02.
Publication Year :
2024

Abstract

Small-ring chemistry is a fascinating field in organic chemistry. gem -Difluorinated cyclopropanes, a unique class of cyclopropanes, have garnered significant interest due to their intrinsic high reactivity. In this context, gem -difluorinated cyclopropanes have been extensively investigated as fluoroallylic synthons in Pd-catalyzed ring-opening/cross-coupling reactions for the synthesis of monofluoroalkenes with linear or branched selectivity. In contrast, Rh-catalysis has revealed diverse selectivity in the reaction of gem -difluorinated cyclopropanes, such as regioselectivity, enantioselectivity, and chemoselectivity. This feature article aims to summarize our efforts towards developing Rh-catalyzed reactions of gem -difluorinated cyclopropanes, briefly discussing the design, selectivity, reaction mechanisms and future research prospects.

Details

Language :
English
ISSN :
1364-548X
Volume :
60
Issue :
28
Database :
MEDLINE
Journal :
Chemical communications (Cambridge, England)
Publication Type :
Academic Journal
Accession number :
38501197
Full Text :
https://doi.org/10.1039/d4cc00793j