Iodo-enamides were synthesised in a single step, in good yield and with complete selectivity from N-formyl imides. The β-iodo-enamides are stable and were converted efficiently into novel geometrically defined β-yn-enamides
Although amides are present in many biological compounds (eg. peptides, drugs,…) and many methods fo...
International audienceOur findings on the bifunctional squaramide-catalyzed enantioselective conjuga...
Demonstrated herein is an unprecedented thioamide-directed cobalt (Co)-catalyzed umpolung annulation...
Iodo-enamides were synthesised in a single step, in good yield and with complete selectivity from N-...
A new method to functionalize enamides via an intermediacy of unsymmetrical 2-amidoallyl cations is ...
The efficient chemo- and regioselective catalytic asymmetric syntheses of enamides, which are import...
Arylations of substituted enamides by aryl iodides were achieved for the first time via an unusual P...
Abstract A novel regio‐ and diastereoselective iron‐catalyzed intermolecular oxyazidation of enamide...
Enamides, dienamides, and enynamides are important building blocks in synthetic, biological, and med...
N-Formamide synthesis using N-formyl imide with primary and secondary amines with catalytic amounts ...
Enamides, dienamides, and enynamides are important building blocks in synthetic, biological, and med...
Regioselective O-alkylation of an amide to form the corresponding imidate is a common synthetic prob...
Primary, secondary and tertiary enaminones react with bis(pyridine)iodonium(I) tetrafluoroborate in ...
Nucleosides and their analogs are pharmacologically important molecules. Here, the authors report an...
direct access to amides from an α-bromo nitroalkane and an amine. Based on its mechanistic bifurcati...
Although amides are present in many biological compounds (eg. peptides, drugs,…) and many methods fo...
International audienceOur findings on the bifunctional squaramide-catalyzed enantioselective conjuga...
Demonstrated herein is an unprecedented thioamide-directed cobalt (Co)-catalyzed umpolung annulation...
Iodo-enamides were synthesised in a single step, in good yield and with complete selectivity from N-...
A new method to functionalize enamides via an intermediacy of unsymmetrical 2-amidoallyl cations is ...
The efficient chemo- and regioselective catalytic asymmetric syntheses of enamides, which are import...
Arylations of substituted enamides by aryl iodides were achieved for the first time via an unusual P...
Abstract A novel regio‐ and diastereoselective iron‐catalyzed intermolecular oxyazidation of enamide...
Enamides, dienamides, and enynamides are important building blocks in synthetic, biological, and med...
N-Formamide synthesis using N-formyl imide with primary and secondary amines with catalytic amounts ...
Enamides, dienamides, and enynamides are important building blocks in synthetic, biological, and med...
Regioselective O-alkylation of an amide to form the corresponding imidate is a common synthetic prob...
Primary, secondary and tertiary enaminones react with bis(pyridine)iodonium(I) tetrafluoroborate in ...
Nucleosides and their analogs are pharmacologically important molecules. Here, the authors report an...
direct access to amides from an α-bromo nitroalkane and an amine. Based on its mechanistic bifurcati...
Although amides are present in many biological compounds (eg. peptides, drugs,…) and many methods fo...
International audienceOur findings on the bifunctional squaramide-catalyzed enantioselective conjuga...
Demonstrated herein is an unprecedented thioamide-directed cobalt (Co)-catalyzed umpolung annulation...
DOI