A redox-neutral avenue to access isoquinolines has been realized by a Co(III)-catalyzed C-H activation process. Starting from readily available N-sulfinyl imine substrates and alkynes, the reaction occurred via N-S cleavage with broad substrate scope and functional group compatibility in the presence of cost-effective cobalt catalysts. (C) 2016, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved
The development of new CH functionalization protocols based on inexpensive cobalt catalysts is curr...
International audienceA facile C-H activation and functionalization of aromatic imines is presented ...
The development of a first row transition metal (cobalt)-based catalyst for the as yet unexplored C–...
Picolinamide has first been employed as a traceless directing group for the cobalt-catalyzed oxidati...
C-H activation assisted by a bifunctional directing group has allowed the construction of heterocycl...
The use of cobalt as catalyst in direct C-H activation protocols as a replacement for more expensive...
N,O-Bidentate directing-enabled, traceless heterocycle synthesis is described via Cp*-free cobalt-ca...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
AbstractTransition-metal-catalyzed isoquinoline synthesis that profits from the strategy of chelatio...
This Ph.D. dissertation describes the synthesis and characterization of bench-top stable aryl-Co(III...
This Ph.D. dissertation describes the synthesis and characterization of bench-top stable aryl-Co(III...
During the past decades, transition metal-catalyzed chelation-assisted C–H bond functionalization ha...
This Ph.D. dissertation describes the synthesis and characterization of bench-top stable aryl-Co(III...
The synthesis of isoquinolines by site-selective CH activation of O-acyl oximes with a Cp*Co-III cat...
The development of new CH functionalization protocols based on inexpensive cobalt catalysts is curr...
International audienceA facile C-H activation and functionalization of aromatic imines is presented ...
The development of a first row transition metal (cobalt)-based catalyst for the as yet unexplored C–...
Picolinamide has first been employed as a traceless directing group for the cobalt-catalyzed oxidati...
C-H activation assisted by a bifunctional directing group has allowed the construction of heterocycl...
The use of cobalt as catalyst in direct C-H activation protocols as a replacement for more expensive...
N,O-Bidentate directing-enabled, traceless heterocycle synthesis is described via Cp*-free cobalt-ca...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
AbstractTransition-metal-catalyzed isoquinoline synthesis that profits from the strategy of chelatio...
This Ph.D. dissertation describes the synthesis and characterization of bench-top stable aryl-Co(III...
This Ph.D. dissertation describes the synthesis and characterization of bench-top stable aryl-Co(III...
During the past decades, transition metal-catalyzed chelation-assisted C–H bond functionalization ha...
This Ph.D. dissertation describes the synthesis and characterization of bench-top stable aryl-Co(III...
The synthesis of isoquinolines by site-selective CH activation of O-acyl oximes with a Cp*Co-III cat...
The development of new CH functionalization protocols based on inexpensive cobalt catalysts is curr...
International audienceA facile C-H activation and functionalization of aromatic imines is presented ...
The development of a first row transition metal (cobalt)-based catalyst for the as yet unexplored C–...