No strain, no gain! The first transition metal-catalyzed enantioselective α-alkylation of cyclobutanones is reported. This method employs palladium catalysis and an electron-deficient PHOX-type ligand to afford all-carbon α-quaternary cyclobutanones in good to excellent yields and enantioselectivities (see scheme)
A catalytic enantioselective method for the synthesis of α-quaternary Mannich-type products is repor...
Contraction action! A simple protocol for the catalytic asymmetric synthesis of highly functionalize...
The enantioselective synthesis of α-disubstituted N-heterocyclic carbonyl compounds has been accompl...
No strain, no gain! The first transition metal-catalyzed enantioselective α-alkylation of cyclobutan...
No strain, no gain! The first transition metal-catalyzed enantioselective α-alkylation of cyclobutan...
The first general method for the enantioselective construction of all-carbon quaternary centers on c...
Contraction action! A simple protocol for the catalytic asymmetric synthesis of highly functionalize...
General catalytic asymmetric routes toward cyclopentanoid and cycloheptanoid core structures embedde...
General catalytic asymmetric routes toward cyclopentanoid and cycloheptanoid core structures embedde...
The first highly enantioselective iridium-catalyzed allylic alkylation providing access to products ...
The first general method for the enantioselective construction of all-carbon quaternary centers on c...
A modular synthesis of enantioenriched polyfunctionalized cyclobutanes was developed that features a...
The first general method for the enantioselective construction of all-carbon quaternary centers on c...
A general method for the synthesis of β-substituted and unsubstituted cycloheptenones bearing enanti...
The first enantioselective Pd-catalyzed construction of all-carbon quaternary stereocenters via 1,4-...
A catalytic enantioselective method for the synthesis of α-quaternary Mannich-type products is repor...
Contraction action! A simple protocol for the catalytic asymmetric synthesis of highly functionalize...
The enantioselective synthesis of α-disubstituted N-heterocyclic carbonyl compounds has been accompl...
No strain, no gain! The first transition metal-catalyzed enantioselective α-alkylation of cyclobutan...
No strain, no gain! The first transition metal-catalyzed enantioselective α-alkylation of cyclobutan...
The first general method for the enantioselective construction of all-carbon quaternary centers on c...
Contraction action! A simple protocol for the catalytic asymmetric synthesis of highly functionalize...
General catalytic asymmetric routes toward cyclopentanoid and cycloheptanoid core structures embedde...
General catalytic asymmetric routes toward cyclopentanoid and cycloheptanoid core structures embedde...
The first highly enantioselective iridium-catalyzed allylic alkylation providing access to products ...
The first general method for the enantioselective construction of all-carbon quaternary centers on c...
A modular synthesis of enantioenriched polyfunctionalized cyclobutanes was developed that features a...
The first general method for the enantioselective construction of all-carbon quaternary centers on c...
A general method for the synthesis of β-substituted and unsubstituted cycloheptenones bearing enanti...
The first enantioselective Pd-catalyzed construction of all-carbon quaternary stereocenters via 1,4-...
A catalytic enantioselective method for the synthesis of α-quaternary Mannich-type products is repor...
Contraction action! A simple protocol for the catalytic asymmetric synthesis of highly functionalize...
The enantioselective synthesis of α-disubstituted N-heterocyclic carbonyl compounds has been accompl...