A new atom-economical strategy to amide linkage from an azide and alcohol liberating hydrogen and nitrogen was developed with an in situ generated ruthenium catalytic system. The reaction has broad substrate generality including diols for the synthesis of cyclic imides
International audienceSelective C-H functionalizations aiming at the formation of new C-N bonds is o...
We report mechanistic studies of C–H activitation/amidation reactions using azides as the amino sour...
A catalytic reaction between aldehydes and primary amides that leads to N-alkylated amides was inves...
A new atom-economical strategy to amide linkage from an azide and alcohol liberating hydrogen and ni...
A new atom-economical strategy to amide linkage from an azide and alcohol liberating hydrogen and ni...
A completely atom-economical and redoxneutral catalytic amide synthesis from an alcohol and a nitril...
A new method for the direct synthesis of imines from alcohols and amines is described where hydrogen...
Direct amide synthesis from alcohols and amines is a highly environmentally friendly process with hi...
An atom-economical and versatile method for the synthesis of cyclic imides from nitriles and diols w...
A completely atom-economical and redox-neutral catalytic amide synthesis from an alcohol and a nitri...
The current existing methods for the amide bond synthesis via acceptorless dehydrogenative coupling ...
A commercially available ruthenium (II) PNP type pincer catalyst (Ru-Macho) promotes formation of am...
Imide derivatives are widely used organic compounds. To address the challenge of atom-economical syn...
A completely atom-economical and redox-neutral catalytic amide synthesis from an alcohol and a nitri...
We report mechanistic studies of C–H activitation/amidation reactions using azides as the amino sour...
International audienceSelective C-H functionalizations aiming at the formation of new C-N bonds is o...
We report mechanistic studies of C–H activitation/amidation reactions using azides as the amino sour...
A catalytic reaction between aldehydes and primary amides that leads to N-alkylated amides was inves...
A new atom-economical strategy to amide linkage from an azide and alcohol liberating hydrogen and ni...
A new atom-economical strategy to amide linkage from an azide and alcohol liberating hydrogen and ni...
A completely atom-economical and redoxneutral catalytic amide synthesis from an alcohol and a nitril...
A new method for the direct synthesis of imines from alcohols and amines is described where hydrogen...
Direct amide synthesis from alcohols and amines is a highly environmentally friendly process with hi...
An atom-economical and versatile method for the synthesis of cyclic imides from nitriles and diols w...
A completely atom-economical and redox-neutral catalytic amide synthesis from an alcohol and a nitri...
The current existing methods for the amide bond synthesis via acceptorless dehydrogenative coupling ...
A commercially available ruthenium (II) PNP type pincer catalyst (Ru-Macho) promotes formation of am...
Imide derivatives are widely used organic compounds. To address the challenge of atom-economical syn...
A completely atom-economical and redox-neutral catalytic amide synthesis from an alcohol and a nitri...
We report mechanistic studies of C–H activitation/amidation reactions using azides as the amino sour...
International audienceSelective C-H functionalizations aiming at the formation of new C-N bonds is o...
We report mechanistic studies of C–H activitation/amidation reactions using azides as the amino sour...
A catalytic reaction between aldehydes and primary amides that leads to N-alkylated amides was inves...
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