The first example of Pd(II)-catalyzed arylation of 2,2′-bipyridine-6-carboxamides via a rollover cyclometalation pathway is reported. A diverse range of (hetero)aryl iodides could be directly coupled with various 2,2′-bipyridine-6-carboxamides in exclusive site-selectivity, which offers a distinct entry to arylated 2,2′-bipyridine-6-carboxamides. A preliminary mechanistic study supports the Pd(II)-rollover cyclometalation pathway
[[abstract]]Treatment of alkenyl and aryl iodides and bromides containing an appropriate α, β-unsatu...
A novel traceless protecting strategy is presented for the long-standing challenge of conducting the...
A new method for palladium-catalyzed β-arylation of aliphatic and cycloaliphatic amides without conv...
The diastereoselective Pd(OAc)<sub>2</sub>-catalyzed, bidentate ligand-directed sp<sup>3</sup> C–H ...
A straightforward Pd(II)-catalyzed general strategy was developed for the C5-selective arylation of...
Palladium(0) complexes formed in situ from a palladium(II) precursor, Pd(OAc)2, proved to be highly ...
This thesis describes our efforts at the discovery, optimization, and mechanistic study of two new a...
This thesis describes our efforts at the discovery, optimization, and mechanistic study of two new a...
The biaryl core has been identified by medicinal chemists as a privileged structure in pharmaceutica...
A ligand-free method for the Pd-catalyzed direct arylation of cyclic enaminones using aryl iodides w...
A new isomerizing ring‐closing amidocarbonylation reaction is reported using Pd catalysis with bulky...
Arylation of 2,6-dichlorobenzaldehyde by aryl boronic acids via site-selective Suzuki coupling catal...
An example of using readily available, less reactive aryl bromides as arylating reagents in the Pd(...
International audienceThe N-tosylcarboxamide group offers the possibility of directing the Pd-cataly...
A new method for palladium-catalyzed β-arylation of aliphatic and cycloaliphatic amides without conv...
[[abstract]]Treatment of alkenyl and aryl iodides and bromides containing an appropriate α, β-unsatu...
A novel traceless protecting strategy is presented for the long-standing challenge of conducting the...
A new method for palladium-catalyzed β-arylation of aliphatic and cycloaliphatic amides without conv...
The diastereoselective Pd(OAc)<sub>2</sub>-catalyzed, bidentate ligand-directed sp<sup>3</sup> C–H ...
A straightforward Pd(II)-catalyzed general strategy was developed for the C5-selective arylation of...
Palladium(0) complexes formed in situ from a palladium(II) precursor, Pd(OAc)2, proved to be highly ...
This thesis describes our efforts at the discovery, optimization, and mechanistic study of two new a...
This thesis describes our efforts at the discovery, optimization, and mechanistic study of two new a...
The biaryl core has been identified by medicinal chemists as a privileged structure in pharmaceutica...
A ligand-free method for the Pd-catalyzed direct arylation of cyclic enaminones using aryl iodides w...
A new isomerizing ring‐closing amidocarbonylation reaction is reported using Pd catalysis with bulky...
Arylation of 2,6-dichlorobenzaldehyde by aryl boronic acids via site-selective Suzuki coupling catal...
An example of using readily available, less reactive aryl bromides as arylating reagents in the Pd(...
International audienceThe N-tosylcarboxamide group offers the possibility of directing the Pd-cataly...
A new method for palladium-catalyzed β-arylation of aliphatic and cycloaliphatic amides without conv...
[[abstract]]Treatment of alkenyl and aryl iodides and bromides containing an appropriate α, β-unsatu...
A novel traceless protecting strategy is presented for the long-standing challenge of conducting the...
A new method for palladium-catalyzed β-arylation of aliphatic and cycloaliphatic amides without conv...