C-H activation assisted by a bifunctional directing group has allowed the construction of heterocycles. This is ideally catalyzed by earth-abundant and eco-friendly transition metals. We report Co(III)-catalyzed redox-neutral coupling between arenes and alkynes using an NH amide as an electrophilic directing group. The redox-neutral C-H activation/coupling afforded quinolines with water as the sole byproduct
Aromatic heterocycles have been identified as effective directing groups (DGs) in C–H functionalizat...
The utility of palladium in cross coupling is driving efforts to find alternatives based on inexpens...
This paper describes the transformation of flat N-containing aromatic compounds (pyridines and quino...
A redox-neutral avenue to access isoquinolines has been realized by a Co(III)-catalyzed C-H activati...
[Cp* Rh-III]-catalyzed C-H activation of arenes assisted by an oxidizing N-O or N-N directing group ...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
The cobalt(III)-catalyzed allylation was developed for amide-directed C–H activation of arenes, het...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
Over the past two decades, extensive investigations into transition metal-catalyzed C–H activation p...
Cobalt(III) and rhodiurn(III) catalysts exhibited complementary scope in C-H amidation of aryl enami...
Alkanes are an abundant and inexpensive source of hydrocarbons; thus, development of new methods to ...
The last decade has been marked by a large increase of demand for green chemistry processes. Consequ...
ABSTRACT: A method for cobalt-catalyzed, aminoquinoline-directed ortho-functionalization of sp2 C−H ...
International audienceA facile C-H activation and functionalization of aromatic imines is presented ...
Aromatic heterocycles have been identified as effective directing groups (DGs) in C–H functionalizat...
Aromatic heterocycles have been identified as effective directing groups (DGs) in C–H functionalizat...
The utility of palladium in cross coupling is driving efforts to find alternatives based on inexpens...
This paper describes the transformation of flat N-containing aromatic compounds (pyridines and quino...
A redox-neutral avenue to access isoquinolines has been realized by a Co(III)-catalyzed C-H activati...
[Cp* Rh-III]-catalyzed C-H activation of arenes assisted by an oxidizing N-O or N-N directing group ...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
The cobalt(III)-catalyzed allylation was developed for amide-directed C–H activation of arenes, het...
Redox-neutral synthesis of isoquinolinium salts via C-H activation of presynthesized or in situ form...
Over the past two decades, extensive investigations into transition metal-catalyzed C–H activation p...
Cobalt(III) and rhodiurn(III) catalysts exhibited complementary scope in C-H amidation of aryl enami...
Alkanes are an abundant and inexpensive source of hydrocarbons; thus, development of new methods to ...
The last decade has been marked by a large increase of demand for green chemistry processes. Consequ...
ABSTRACT: A method for cobalt-catalyzed, aminoquinoline-directed ortho-functionalization of sp2 C−H ...
International audienceA facile C-H activation and functionalization of aromatic imines is presented ...
Aromatic heterocycles have been identified as effective directing groups (DGs) in C–H functionalizat...
Aromatic heterocycles have been identified as effective directing groups (DGs) in C–H functionalizat...
The utility of palladium in cross coupling is driving efforts to find alternatives based on inexpens...
This paper describes the transformation of flat N-containing aromatic compounds (pyridines and quino...