An Ir‐catalyzed C(sp3)−H alkynylation of aliphatic ketones, aldehydes, and alcohols was achieved by using the corresponding oxime derivatives and a IrIII catalyst. This general reaction is selective towards primary C(sp3)−H bonds and can be used for the late‐stage C−H alkynylation of complex molecules
International audienceA versatile iridium(III) metallacycle catalyses rapidly and selectively the re...
[Cp*Ir(Pro)Cl] (Pro = prolinato) was identified among a series of Cp*–iridium half-sandwich complexe...
Mild and efficient synthesis of ynones via Ir(III)- and Rh(III)-catalyzed, chelation-assisted form...
PubMed: 294320022-s2.0-85042858918A highly effective and green procedure for the formation of ?-alky...
A highly effective and green procedure for the formation of ?-alkylated ketones has been disclosed v...
Selective C–H bond alkynylation toward modular access to material and pharmaceutical molecules is of...
WOS: 000426803300038PubMed ID: 29432002A highly effective and green procedure for the formation of a...
The first α-alkylation of unactivated amides with primary alcohols is described. An effective and ro...
The first α-alkylation of unactivated amides with primary alcohols is described. An effective and ro...
A Cp*Ir complex bearing a functional bipyridonate ligand was found to be a highly effective and vers...
A new strategy for the synthesis of α-alkylated ketones via tandem acceptorless dehydrogenation/α-al...
International audienceA versatile iridium(III) metallacycle catalyses rapidly and selectively the re...
International audienceA versatile iridium(III) metallacycle catalyses rapidly and selectively the re...
International audienceA versatile iridium(III) metallacycle catalyses rapidly and selectively the re...
The directed C–H alkynylation of 2-(hetero)arylquinazolin-4-ones has been explored with the ethynyl...
International audienceA versatile iridium(III) metallacycle catalyses rapidly and selectively the re...
[Cp*Ir(Pro)Cl] (Pro = prolinato) was identified among a series of Cp*–iridium half-sandwich complexe...
Mild and efficient synthesis of ynones via Ir(III)- and Rh(III)-catalyzed, chelation-assisted form...
PubMed: 294320022-s2.0-85042858918A highly effective and green procedure for the formation of ?-alky...
A highly effective and green procedure for the formation of ?-alkylated ketones has been disclosed v...
Selective C–H bond alkynylation toward modular access to material and pharmaceutical molecules is of...
WOS: 000426803300038PubMed ID: 29432002A highly effective and green procedure for the formation of a...
The first α-alkylation of unactivated amides with primary alcohols is described. An effective and ro...
The first α-alkylation of unactivated amides with primary alcohols is described. An effective and ro...
A Cp*Ir complex bearing a functional bipyridonate ligand was found to be a highly effective and vers...
A new strategy for the synthesis of α-alkylated ketones via tandem acceptorless dehydrogenation/α-al...
International audienceA versatile iridium(III) metallacycle catalyses rapidly and selectively the re...
International audienceA versatile iridium(III) metallacycle catalyses rapidly and selectively the re...
International audienceA versatile iridium(III) metallacycle catalyses rapidly and selectively the re...
The directed C–H alkynylation of 2-(hetero)arylquinazolin-4-ones has been explored with the ethynyl...
International audienceA versatile iridium(III) metallacycle catalyses rapidly and selectively the re...
[Cp*Ir(Pro)Cl] (Pro = prolinato) was identified among a series of Cp*–iridium half-sandwich complexe...
Mild and efficient synthesis of ynones via Ir(III)- and Rh(III)-catalyzed, chelation-assisted form...