International audienceTandem iron/zinc or iron/indium-catalysed reductions of various primary amides to amines under hydrosilylation conditions are reported under visible light activation. By a simple modification of the nature of the co-catalyst (Zn(OTf)2 vs In(OTf)3), Fe(CO)4(IMes) can promote the high chemoselective reduction of primary amides into primary amines (21 examples, up to 93% isolated yields) and secondary amines (8 examples, up to 51% isolated yields), respectively. Notably, both benzamide and alkanamide derivatives can be reduced
The partial reduction of amides is a challenging transformation that must overcome the intrinsic sta...
International audienceAn efficient method for the reductive amination of carbonyl derivatives with ω...
A new iron-catalysed oxidative amidation of differently substituted benzylic alcohols with mono- and...
International audienceIron comes first, second, and third: By using the well-defined Cp-IMes iron ca...
Reduction of nitriles to silylated primary amines was achieved by combination of 1,1,3,3-tetramethyl...
Diethylzinc (Et<sub>2</sub>Zn) can be used as an efficient and chemoselective catalyst for the reduc...
This thesis covers the development of catalytic methodologies for the mild and chemoselective reduct...
Low-cost zinc is employed as a catalyst along with triethylsilane (TES) in a simple, straightforward...
International audienceSelective reduction of carboxylic acids either to aldehydes or alcohols is ach...
International audienceHydrosilylation of secondary and tertiary amides to amines is described using ...
A base-metal, Fe(0)-catalyzed hydrosilylation of imines to obtain amines is reported here which outp...
International audienceAmines are among the most important compounds due to their wide applications i...
International audienceA general and efficient hydrosilylation of imines catalysed by a well defined ...
International audienceThe partial reduction of amides is a challenging transformation that must over...
Ketones and imines are chemoselectively reduced at room temperature in methanol to the corresponding...
The partial reduction of amides is a challenging transformation that must overcome the intrinsic sta...
International audienceAn efficient method for the reductive amination of carbonyl derivatives with ω...
A new iron-catalysed oxidative amidation of differently substituted benzylic alcohols with mono- and...
International audienceIron comes first, second, and third: By using the well-defined Cp-IMes iron ca...
Reduction of nitriles to silylated primary amines was achieved by combination of 1,1,3,3-tetramethyl...
Diethylzinc (Et<sub>2</sub>Zn) can be used as an efficient and chemoselective catalyst for the reduc...
This thesis covers the development of catalytic methodologies for the mild and chemoselective reduct...
Low-cost zinc is employed as a catalyst along with triethylsilane (TES) in a simple, straightforward...
International audienceSelective reduction of carboxylic acids either to aldehydes or alcohols is ach...
International audienceHydrosilylation of secondary and tertiary amides to amines is described using ...
A base-metal, Fe(0)-catalyzed hydrosilylation of imines to obtain amines is reported here which outp...
International audienceAmines are among the most important compounds due to their wide applications i...
International audienceA general and efficient hydrosilylation of imines catalysed by a well defined ...
International audienceThe partial reduction of amides is a challenging transformation that must over...
Ketones and imines are chemoselectively reduced at room temperature in methanol to the corresponding...
The partial reduction of amides is a challenging transformation that must overcome the intrinsic sta...
International audienceAn efficient method for the reductive amination of carbonyl derivatives with ω...
A new iron-catalysed oxidative amidation of differently substituted benzylic alcohols with mono- and...