The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to alpha,beta-unsaturated aldehydes, ketones, and esters is described. For cyclic substrates, excellent chemo-, regio-, and enantioselectivities are achieved when a Pd(O2CCF3)(2)/DuPHOS catalyst is applied.</p
The development and optimization of a palladium-catalyzed asymmetric conjugate addition of arylboron...
The first enantioselective Pd-catalyzed construction of all-carbon quaternary stereocenters via 1,4-...
Flava Flavanone: Asymmetric conjugate additions to chromones and 4-quinolones are reported utilizing...
The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to alpha,beta-unsat...
The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to alpha,beta-unsat...
The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to alpha,beta-unsat...
The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to α,β-unsaturated ...
The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to alpha,beta-unsat...
This account describes our laboratory’s efforts in the development of a palladium-catalyzed asymmetr...
This account describes our laboratory’s efforts in the development of a palladium-catalyzed asymmetr...
An asymmetric palladium-catalyzed conjugate addition reaction of arylboronic acids to enone substrat...
Enantioselective conjugate additions of arylboronic acids to β-substituted cyclic enones have been p...
Flava Flavanone: Asymmetric conjugate additions to chromones and 4-quinolones are reported utilizing...
The first enantioselective Pd-catalyzed construction of all-carbon quaternary stereocenters via 1,4-...
The development and optimization of a palladium-catalyzed asymmetric conjugate addition of arylboron...
The development and optimization of a palladium-catalyzed asymmetric conjugate addition of arylboron...
The first enantioselective Pd-catalyzed construction of all-carbon quaternary stereocenters via 1,4-...
Flava Flavanone: Asymmetric conjugate additions to chromones and 4-quinolones are reported utilizing...
The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to alpha,beta-unsat...
The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to alpha,beta-unsat...
The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to alpha,beta-unsat...
The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to α,β-unsaturated ...
The first asymmetric palladium-catalyzed conjugate addition of arylboronic acids to alpha,beta-unsat...
This account describes our laboratory’s efforts in the development of a palladium-catalyzed asymmetr...
This account describes our laboratory’s efforts in the development of a palladium-catalyzed asymmetr...
An asymmetric palladium-catalyzed conjugate addition reaction of arylboronic acids to enone substrat...
Enantioselective conjugate additions of arylboronic acids to β-substituted cyclic enones have been p...
Flava Flavanone: Asymmetric conjugate additions to chromones and 4-quinolones are reported utilizing...
The first enantioselective Pd-catalyzed construction of all-carbon quaternary stereocenters via 1,4-...
The development and optimization of a palladium-catalyzed asymmetric conjugate addition of arylboron...
The development and optimization of a palladium-catalyzed asymmetric conjugate addition of arylboron...
The first enantioselective Pd-catalyzed construction of all-carbon quaternary stereocenters via 1,4-...
Flava Flavanone: Asymmetric conjugate additions to chromones and 4-quinolones are reported utilizing...
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