A palladium-catalyzed dehydrogenative coupling between diarylamines and olefins has been discovered for the synthesis of substituted indoles. This intermolecular annulation approach incorporates readily available olefins for the first time and obviates the need of any additional directing group. An ortho palladation, olefin coordination, and beta-migratory insertion sequence has been proposed for the generation of olefinated intermediate, which is found to produce the expected indole moiety
A palladium-catalyzed 3-component synthesis of 3-(diarylmethylene)indolin-2-ones was developed. A se...
A palladium-catalyzed 1,2-carboamination through C–H activation at room temperature is reported for ...
H-substituted imines are elusive compounds formed when aldehydes or ketones are mixed with ammonia. ...
A palladium-catalyzed dehydrogenative coupling between diarylamines and olefins has been discovered ...
In an effort to obtain more efficient and greener chemical transformations, a substantial amount of ...
Tandem palladium-catalysed aryl and alkenyl C-N bond formation allows the synthesis of a variety of ...
(Chemical Equation Presented) A single tandem operation allows rapid access to a variety of substitu...
A palladium-catalyzed CH activation strategy has been successfully employed for exclusive synthesis ...
This review highlights the development of palladium-catalyzed C-H and N-H functionalization reaction...
The Lautens group has developed many late transition-metal catalyzed protocols for the synthesis of ...
The substituted indole nucleus [indole is the acronym from indigo (the natural dye) and oleum (used ...
In this thesis, various approaches from the literature employing carbon–hydrogen bond activation for...
A novel palladium catalyzed approach to 3-arylindoles was developed from indoles and cyclohexanones....
Pd doles it out: A palladium-catalyzed approach to indoles using the title reaction was achieved (se...
In an effort to obtain more efficient and greener chemical transformations, a substantial amount of ...
A palladium-catalyzed 3-component synthesis of 3-(diarylmethylene)indolin-2-ones was developed. A se...
A palladium-catalyzed 1,2-carboamination through C–H activation at room temperature is reported for ...
H-substituted imines are elusive compounds formed when aldehydes or ketones are mixed with ammonia. ...
A palladium-catalyzed dehydrogenative coupling between diarylamines and olefins has been discovered ...
In an effort to obtain more efficient and greener chemical transformations, a substantial amount of ...
Tandem palladium-catalysed aryl and alkenyl C-N bond formation allows the synthesis of a variety of ...
(Chemical Equation Presented) A single tandem operation allows rapid access to a variety of substitu...
A palladium-catalyzed CH activation strategy has been successfully employed for exclusive synthesis ...
This review highlights the development of palladium-catalyzed C-H and N-H functionalization reaction...
The Lautens group has developed many late transition-metal catalyzed protocols for the synthesis of ...
The substituted indole nucleus [indole is the acronym from indigo (the natural dye) and oleum (used ...
In this thesis, various approaches from the literature employing carbon–hydrogen bond activation for...
A novel palladium catalyzed approach to 3-arylindoles was developed from indoles and cyclohexanones....
Pd doles it out: A palladium-catalyzed approach to indoles using the title reaction was achieved (se...
In an effort to obtain more efficient and greener chemical transformations, a substantial amount of ...
A palladium-catalyzed 3-component synthesis of 3-(diarylmethylene)indolin-2-ones was developed. A se...
A palladium-catalyzed 1,2-carboamination through C–H activation at room temperature is reported for ...
H-substituted imines are elusive compounds formed when aldehydes or ketones are mixed with ammonia. ...