A Pd-catalyzed three-component reaction of N-tosylhydrazone, terminal alkyne, and aryl halide follows a mechanism involving a sequence of Pd carbene migratory insertion-trans-metalation reductive elimination, leading to the formation of one sp(2)-sp(3) C-C bond and one sp-sp(3) C-C bond.Chemistry, MultidisciplinarySCI(E)PubMed81ARTICLE3913590-1359113
A palladium‐catalyzed carbene insertion into C(sp3)−H bonds leading to pyrrolidines was developed. T...
Cyclopropylmethyl palladium species can be accessed by Pd-catalyzed reaction of either cyclopropyl <...
A Pd-catalyzed stereoselective synthesis of 3-vinylindoles and 3-vinylbenzofurans has been developed...
In Chapter 1, an overview of the literature of palladium-catalyzed carbenylative coupling reaction w...
Pd-catalyzed reaction of N-tosylhydrazones with benzyl halides affords di- and trisubstituted olefin...
The Pd-catalyzed reaction of N-tosylhydrazones and arylboronic acids provides olefin derivatives. Th...
A palladium-catalyzed three-component reaction of N-tosylhydrazone, norbornene and aryl halide has b...
Transition-metal-catalyzed carbene transformations and cross-couplings represent two major reaction ...
A palladium-catalyzed reductive coupling between N-tosylhydrazones and aryl bromides has been develo...
Palladium-catalyzed reductive coupling reactions between N-tosylhydrazones and aryl halides lead to ...
Virtually all of the top pharmaceuticals sold today require the use of organic synthesis, the develo...
Alkyl Chromium(0) carbene complexes typically undergo cycloaddition with alkynes to afford carbo- or...
Cyclopropylmethyl palladium species can be accessed by Pd-catalyzed reaction of either cyclopropyl N...
-Halo-N-tosylhydrazones are explored as reagents for the multiple carbon-carbon bond formations in p...
Pd-catalyzed cross-coupling of halides with CF3-substituted diazo compounds or N-tosylhydrazones has...
A palladium‐catalyzed carbene insertion into C(sp3)−H bonds leading to pyrrolidines was developed. T...
Cyclopropylmethyl palladium species can be accessed by Pd-catalyzed reaction of either cyclopropyl <...
A Pd-catalyzed stereoselective synthesis of 3-vinylindoles and 3-vinylbenzofurans has been developed...
In Chapter 1, an overview of the literature of palladium-catalyzed carbenylative coupling reaction w...
Pd-catalyzed reaction of N-tosylhydrazones with benzyl halides affords di- and trisubstituted olefin...
The Pd-catalyzed reaction of N-tosylhydrazones and arylboronic acids provides olefin derivatives. Th...
A palladium-catalyzed three-component reaction of N-tosylhydrazone, norbornene and aryl halide has b...
Transition-metal-catalyzed carbene transformations and cross-couplings represent two major reaction ...
A palladium-catalyzed reductive coupling between N-tosylhydrazones and aryl bromides has been develo...
Palladium-catalyzed reductive coupling reactions between N-tosylhydrazones and aryl halides lead to ...
Virtually all of the top pharmaceuticals sold today require the use of organic synthesis, the develo...
Alkyl Chromium(0) carbene complexes typically undergo cycloaddition with alkynes to afford carbo- or...
Cyclopropylmethyl palladium species can be accessed by Pd-catalyzed reaction of either cyclopropyl N...
-Halo-N-tosylhydrazones are explored as reagents for the multiple carbon-carbon bond formations in p...
Pd-catalyzed cross-coupling of halides with CF3-substituted diazo compounds or N-tosylhydrazones has...
A palladium‐catalyzed carbene insertion into C(sp3)−H bonds leading to pyrrolidines was developed. T...
Cyclopropylmethyl palladium species can be accessed by Pd-catalyzed reaction of either cyclopropyl <...
A Pd-catalyzed stereoselective synthesis of 3-vinylindoles and 3-vinylbenzofurans has been developed...