A regio-and diastereoselective carbometalation of easily accessible CF 3-substituted cyclopropenes is developed with a diastereoselectivity of the addition opposite to the CF 3 group. This simple strategy allows the preparation of polysubstituted (up to penta-) cyclopropyl rings possessing two adjacent quaternary carbon stereocenters with excellent diastereoselectivities
Diastereoselective cyclopropanation of a trans-substituted vinyl cyclopropane was studied. The stere...
The diastereoselective carbocupration reaction of alkoxy-functionalized cyclopropene derivatives, fo...
We herein disclose a diastereoselective ring opening of non-donor–acceptor cyclopropanes via an intr...
A regio-and diastereoselective carbometalation of easily accessible CF 3-substituted cyclopropenes i...
International audienceNew chiral fluorinated reagents (N-(dibromofluoroacetyl)oxazolidinones) were e...
International audienceThe diastereoselective carbocupration reaction of cyclopropenylmethyl ethers f...
Cyclopropanation of [2-(alkenyl)pentenediyl]Fe(CO)3 complexes (4) proceeds in a diastereoselective f...
In a departure from the current trend of using metal-catalyzed routes to cyclopropanation, pentosyl ...
International audienceThe synthesis of highly functionalized monofluorinated cyclopropanes based on ...
The synthesis of highly functionalized monofluorinated cyclopropanes based on a Michael Initiated Ri...
The stereoselective preparation of three stereoisomeric tercyclopropanes and a quinquecyclopropane w...
Suitably designed vinyl sulfone-modified furanosides act as substrates for Michael initiated ring cl...
The diastereoselective cyclopropanation of three stereoisomerically unique vinylcyclopropanes was st...
A convenient and novel domino reaction for the synthesis of highly functionalized cyclopropanes is r...
A highly diastereoselective cyclopropanation protocol has been employed in the syntheses of trans-SC...
Diastereoselective cyclopropanation of a trans-substituted vinyl cyclopropane was studied. The stere...
The diastereoselective carbocupration reaction of alkoxy-functionalized cyclopropene derivatives, fo...
We herein disclose a diastereoselective ring opening of non-donor–acceptor cyclopropanes via an intr...
A regio-and diastereoselective carbometalation of easily accessible CF 3-substituted cyclopropenes i...
International audienceNew chiral fluorinated reagents (N-(dibromofluoroacetyl)oxazolidinones) were e...
International audienceThe diastereoselective carbocupration reaction of cyclopropenylmethyl ethers f...
Cyclopropanation of [2-(alkenyl)pentenediyl]Fe(CO)3 complexes (4) proceeds in a diastereoselective f...
In a departure from the current trend of using metal-catalyzed routes to cyclopropanation, pentosyl ...
International audienceThe synthesis of highly functionalized monofluorinated cyclopropanes based on ...
The synthesis of highly functionalized monofluorinated cyclopropanes based on a Michael Initiated Ri...
The stereoselective preparation of three stereoisomeric tercyclopropanes and a quinquecyclopropane w...
Suitably designed vinyl sulfone-modified furanosides act as substrates for Michael initiated ring cl...
The diastereoselective cyclopropanation of three stereoisomerically unique vinylcyclopropanes was st...
A convenient and novel domino reaction for the synthesis of highly functionalized cyclopropanes is r...
A highly diastereoselective cyclopropanation protocol has been employed in the syntheses of trans-SC...
Diastereoselective cyclopropanation of a trans-substituted vinyl cyclopropane was studied. The stere...
The diastereoselective carbocupration reaction of alkoxy-functionalized cyclopropene derivatives, fo...
We herein disclose a diastereoselective ring opening of non-donor–acceptor cyclopropanes via an intr...