An enantioselective copper-catalyzed arylation of tertiary carbon-centered radicals, leading to quaternary all-carbon stereocenters, has been developed herein. The tertiary carbon-centered radicals, including both benzylic and nonbenzylic radicals, were produced by the addition of trifluoromethyl radical to α-substituted acrylamides, and subsequently captured by chiral aryl copper(II) species to give C–Ar bonds with excellent enantioselectivity. Importantly, an acylamidyl (CONHAr) group adjacent to the tertiary carbon radical is essential for the asymmetric radical coupling. The reaction itself features broad substrate scope, excellent functional group compatibility and mild conditions
International audienceThe copper-catalyzed conjugate addition of Grignard reagents to 3-substituted ...
Copper-catalyzed enantioselective 1,4-conjugate addition of methyl 4,4,4-trifluorocrotonate with ali...
Suzuki–Miyaura couplings of tertiary-alkyl moieties are accomplished in the presence of a copper cat...
An enantioselective copper-catalyzed arylation of tertiary carbon-centered radicals, leading to quat...
The highly enantioselective copper(I)/N-heterocyclic carbene (NHC) catalyzed synthesis of di- and tr...
A copper/phosphoramidite catalyzed asymmetric allylic alkylation of Z trisubstituted allyl bromides ...
The copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted cyclic eno...
A good choice: A new catalytic method was found for the construction of stereogenic quaternary carbo...
The copper-catalyzed conjugate addition of various Grignard reagents to polyconjugated enones (dieno...
International audienceThe copper-catalyzed conjugate addition of various Grignard reagents to polyco...
International audienceThe catalytic asymmetric synthesis of β‐trifluoromethylated esters or nitriles...
Pure and simple: Alkylzirconocenes generated in situ from simple alkenes are used in highly enantios...
An efficient and highly enantioselective copper-catalyzed allylic alkylation of disubstituted allyl ...
The copper-catalyzed conjugate addition of Grignard reagents to 3-substituted cyclic enones allows t...
International audienceThe copper-catalyzed conjugate addition of Grignard reagents to 3-substituted ...
Copper-catalyzed enantioselective 1,4-conjugate addition of methyl 4,4,4-trifluorocrotonate with ali...
Suzuki–Miyaura couplings of tertiary-alkyl moieties are accomplished in the presence of a copper cat...
An enantioselective copper-catalyzed arylation of tertiary carbon-centered radicals, leading to quat...
The highly enantioselective copper(I)/N-heterocyclic carbene (NHC) catalyzed synthesis of di- and tr...
A copper/phosphoramidite catalyzed asymmetric allylic alkylation of Z trisubstituted allyl bromides ...
The copper-catalyzed asymmetric conjugate addition of Grignard reagents to trisubstituted cyclic eno...
A good choice: A new catalytic method was found for the construction of stereogenic quaternary carbo...
The copper-catalyzed conjugate addition of various Grignard reagents to polyconjugated enones (dieno...
International audienceThe copper-catalyzed conjugate addition of various Grignard reagents to polyco...
International audienceThe catalytic asymmetric synthesis of β‐trifluoromethylated esters or nitriles...
Pure and simple: Alkylzirconocenes generated in situ from simple alkenes are used in highly enantios...
An efficient and highly enantioselective copper-catalyzed allylic alkylation of disubstituted allyl ...
The copper-catalyzed conjugate addition of Grignard reagents to 3-substituted cyclic enones allows t...
International audienceThe copper-catalyzed conjugate addition of Grignard reagents to 3-substituted ...
Copper-catalyzed enantioselective 1,4-conjugate addition of methyl 4,4,4-trifluorocrotonate with ali...
Suzuki–Miyaura couplings of tertiary-alkyl moieties are accomplished in the presence of a copper cat...