International audienceAn efficient access to highly functionalized monofluorocyclopropanes is described. The developed methodology allowed straightforward access to a large panel of polysubstituted fluorinated cyclopropanes in good to excellent yields and good diastereoselectivities. The Rh-catalyzed cyclopropanation proved to be efficient on several fluorinated olefins and several diazo compounds. This method represents the first general route to complex fluorinated cyclopropanes
Herein, we report a Rh-catalyzed carbofluorination of alkenes using gem-difluorinated cyclopropanes ...
A rhodium-catalyzed cyclopropanation of 1-fluoro-1-(phenylsulfonyl)ethylene and diazo esters is des...
International audienceThe catalytic asymmetric synthesis of mono-fluoro-, -chloro- and -bromomethyl-...
International audienceAn efficient access to highly functionalized monofluorocyclopropanes is descri...
International audienceAn efficient access to highly functionalized monofluorocyclopropanes is descri...
International audienceAn efficient access to highly functionalized monofluorocyclopropanes is descri...
An efficient access to highly functionalized monofluorocyclopropanes is described. The developed met...
The synthesis of trifluoromethylated cyclopropenes is very important for applications in drug discov...
International audienceThe first catalytic asymmetric synthesis of highly functionalized difluorometh...
International audienceThe first catalytic asymmetric synthesis of highly functionalized difluorometh...
Make it strained and fluorinated! A rhodium-catalyzed domino diazotization/cyclopropenation reaction...
International audienceAn efficient catalytic enantioselective access to chiral functionalized triflu...
International audienceThe combination of a fluorine atom and a cyclopropane ring, which both possess...
International audienceThe combination of a fluorine atom and a cyclopropane ring, which both possess...
International audienceThe combination of a fluorine atom and a cyclopropane ring, which both possess...
Herein, we report a Rh-catalyzed carbofluorination of alkenes using gem-difluorinated cyclopropanes ...
A rhodium-catalyzed cyclopropanation of 1-fluoro-1-(phenylsulfonyl)ethylene and diazo esters is des...
International audienceThe catalytic asymmetric synthesis of mono-fluoro-, -chloro- and -bromomethyl-...
International audienceAn efficient access to highly functionalized monofluorocyclopropanes is descri...
International audienceAn efficient access to highly functionalized monofluorocyclopropanes is descri...
International audienceAn efficient access to highly functionalized monofluorocyclopropanes is descri...
An efficient access to highly functionalized monofluorocyclopropanes is described. The developed met...
The synthesis of trifluoromethylated cyclopropenes is very important for applications in drug discov...
International audienceThe first catalytic asymmetric synthesis of highly functionalized difluorometh...
International audienceThe first catalytic asymmetric synthesis of highly functionalized difluorometh...
Make it strained and fluorinated! A rhodium-catalyzed domino diazotization/cyclopropenation reaction...
International audienceAn efficient catalytic enantioselective access to chiral functionalized triflu...
International audienceThe combination of a fluorine atom and a cyclopropane ring, which both possess...
International audienceThe combination of a fluorine atom and a cyclopropane ring, which both possess...
International audienceThe combination of a fluorine atom and a cyclopropane ring, which both possess...
Herein, we report a Rh-catalyzed carbofluorination of alkenes using gem-difluorinated cyclopropanes ...
A rhodium-catalyzed cyclopropanation of 1-fluoro-1-(phenylsulfonyl)ethylene and diazo esters is des...
International audienceThe catalytic asymmetric synthesis of mono-fluoro-, -chloro- and -bromomethyl-...