International audienceAn efficient iridium-catalyzed C(sp2)−H reaction of non-aromatic tertiary enamides was successfully developed under mild reaction conditions and with high regioselectivity, leading to original C-3 borylated enamides in good yields. These derivatives could then be exploited in Suzuki cross-coupling reactions, or converted into valuable 3,3-dihalogenopiperidine derivatives through short reaction times with moderate to good yields
International audienceStarting from 5,5′-dihalo-1′-pentyl-2H-spiro[furo[2,3-b]pyridine-3,3′-indolin]...
The appropriate design of a ligand (L) in IrCl(CO)(L)<sub>2</sub> (<b>4</b>) realized the efficien...
An iridium-catalyzed C–H borylation provides the key step in a short synthesis of two indolequinone ...
International audienceAn efficient iridium-catalyzed C(sp2)−H reaction of non-aromatic tertiary enam...
Studies on the deactivation mechanism of the reaction of N,N-dialkylamides with TMDS catalyzed by Va...
Optically active organoboronic acids and their derivatives are an important family of target compoun...
Transition metal catalysed C-H activation is a highly desirable strategy for the functionalization o...
An efficient functionalization of aromatic main-chain polymers was established using a combination o...
A mild, regioselective, iridium-catalyzed C–H amidation and borylation of anthraquinones to the o-su...
The catalytic, undirected borylation of alkyl C–H bonds typically occurs at high reaction temperatur...
The tetrasubstituted prochiral amido-alkenes (1a, b), (2a, b), and (3b) have been homogeneously hydr...
An iridium-catalyzed regioselective C-H borylation of pentafluoroaniline-derived heteroaromatic aldi...
A mechanistic study on the origin of the difference in reactivity between Ir catalysts for C-H boryl...
Iridium catalysed C-H borylation has moved from an interesting observation to an efficient catalytic...
The preformed catalyst [Ir(Cl)(COD)(1,10-phenanthroline)] (<b>2</b>; COD = cyclooctadiene) was fo...
International audienceStarting from 5,5′-dihalo-1′-pentyl-2H-spiro[furo[2,3-b]pyridine-3,3′-indolin]...
The appropriate design of a ligand (L) in IrCl(CO)(L)<sub>2</sub> (<b>4</b>) realized the efficien...
An iridium-catalyzed C–H borylation provides the key step in a short synthesis of two indolequinone ...
International audienceAn efficient iridium-catalyzed C(sp2)−H reaction of non-aromatic tertiary enam...
Studies on the deactivation mechanism of the reaction of N,N-dialkylamides with TMDS catalyzed by Va...
Optically active organoboronic acids and their derivatives are an important family of target compoun...
Transition metal catalysed C-H activation is a highly desirable strategy for the functionalization o...
An efficient functionalization of aromatic main-chain polymers was established using a combination o...
A mild, regioselective, iridium-catalyzed C–H amidation and borylation of anthraquinones to the o-su...
The catalytic, undirected borylation of alkyl C–H bonds typically occurs at high reaction temperatur...
The tetrasubstituted prochiral amido-alkenes (1a, b), (2a, b), and (3b) have been homogeneously hydr...
An iridium-catalyzed regioselective C-H borylation of pentafluoroaniline-derived heteroaromatic aldi...
A mechanistic study on the origin of the difference in reactivity between Ir catalysts for C-H boryl...
Iridium catalysed C-H borylation has moved from an interesting observation to an efficient catalytic...
The preformed catalyst [Ir(Cl)(COD)(1,10-phenanthroline)] (<b>2</b>; COD = cyclooctadiene) was fo...
International audienceStarting from 5,5′-dihalo-1′-pentyl-2H-spiro[furo[2,3-b]pyridine-3,3′-indolin]...
The appropriate design of a ligand (L) in IrCl(CO)(L)<sub>2</sub> (<b>4</b>) realized the efficien...
An iridium-catalyzed C–H borylation provides the key step in a short synthesis of two indolequinone ...