This review describes the development of enantioselective methods for the ring opening of cyclopropanes. Both approaches based on the reaction of nonchiral cyclopropanes and (dynamic) kinetic resolutions and asymmetric transformations of chiral substrates are presented. The review is organized according to substrate classes, starting by the more mature field of donor–acceptor cyclopropanes. Emerging methods for enantioselective ring opening of acceptor- or donor-only cyclopropanes are then presented. The last part of the review describes the ring opening of more reactive three-membered rings substituted with unsaturations with a particular focus on vinylcyclopropanes, alkylidenecyclopropanes, and vinylidenecyclopropanes. In the last two dec...
The aim of this research is to develop new Phase-Transfer catalysed Michael and Michael tandem react...
Cyclopropanes are found in an array of synthetic and natural products. The Simmons-Smith reaction ha...
This project has received funding from the European Research Council (ERC) under the European Union'...
Cyclopropanes are strained carbocycles that can undergo ring opening reactions in which one of the C...
Both physical and organic chemists are interested in the cyclopropane ring, the former owing to the ...
A double synergistic cascade reaction is reported merging transition metal and amine catalysis. The ...
International audienceThe first catalytic asymmetric synthesis of highly functionalized difluorometh...
The herein reported visible-light-activated catalytic asymmetric [3+2] photocycloadditions between c...
International audienceA catalytic asymmetric synthesis of halocyclopropanes is described. The develo...
In this review, we present the recent advances in the synthesis and reactivity of vinylcyclopropanes...
Use of metal complexes of chiral nonracemic ligands in asymmetric cyclopropanation reactions via hom...
Palladium-catalyzed asymmetric formal [3+2] cycloaddition of vinyl cyclopropanes and β,γ-unsaturated...
International audienceAn efficient catalytic enantioselective access to chiral functionalized triflu...
<div><p>Ring-opening hydroarylation of cyclopropanes is typically limited to substrates bearing a do...
We present a formal [3+2] cycloaddition based on synergistic catalysis. Vinylcyclopropanes derived f...
The aim of this research is to develop new Phase-Transfer catalysed Michael and Michael tandem react...
Cyclopropanes are found in an array of synthetic and natural products. The Simmons-Smith reaction ha...
This project has received funding from the European Research Council (ERC) under the European Union'...
Cyclopropanes are strained carbocycles that can undergo ring opening reactions in which one of the C...
Both physical and organic chemists are interested in the cyclopropane ring, the former owing to the ...
A double synergistic cascade reaction is reported merging transition metal and amine catalysis. The ...
International audienceThe first catalytic asymmetric synthesis of highly functionalized difluorometh...
The herein reported visible-light-activated catalytic asymmetric [3+2] photocycloadditions between c...
International audienceA catalytic asymmetric synthesis of halocyclopropanes is described. The develo...
In this review, we present the recent advances in the synthesis and reactivity of vinylcyclopropanes...
Use of metal complexes of chiral nonracemic ligands in asymmetric cyclopropanation reactions via hom...
Palladium-catalyzed asymmetric formal [3+2] cycloaddition of vinyl cyclopropanes and β,γ-unsaturated...
International audienceAn efficient catalytic enantioselective access to chiral functionalized triflu...
<div><p>Ring-opening hydroarylation of cyclopropanes is typically limited to substrates bearing a do...
We present a formal [3+2] cycloaddition based on synergistic catalysis. Vinylcyclopropanes derived f...
The aim of this research is to develop new Phase-Transfer catalysed Michael and Michael tandem react...
Cyclopropanes are found in an array of synthetic and natural products. The Simmons-Smith reaction ha...
This project has received funding from the European Research Council (ERC) under the European Union'...