Epoxides undergo smooth ring-opening with aryl amines in 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim]BF4) or 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim]PF6) ionic liquids under mild and neutral conditions to afford the corresponding β-amino alcohols in excellent yields with high regioselectivity
Alcohols undergo smooth oxidation with iodoxybenzoic acid (IBX) or with Dess-Martin-Periodinane (DMP...
A mild, efficient, and eco-friendly procedure for the conversion of aliphatic, alicyclic and aromati...
Aryl imines, derived in situ from aldehydes and amines, smoothly undergo addition with trimethylsily...
Abstract The epoxides undergo ring-opening reaction smoothly with various amines in an ionic liquid ...
Aziridines undergo ring opening smoothly with various arylamines in 1-butyl-3-methylimidazolium tetr...
One-pot condensation from aromatic aldehyde, methyl ketone, malononitrile and ammonium acetate in th...
AbstractOne-pot condensation from aromatic aldehyde, methyl ketone, malononitrile and ammonium aceta...
Oxiranes undergo ring opening rapidly with sodium azide in a [bmim]BF<SUB>4</SUB>/H<SUB>2</SUB>O or ...
A variety of structurally diverse epoxides undergo facile cleavages by ionic liquid, [AcMIm]X withou...
The imines derived in situ from aldehydes and amines undergo smoothly nucleophilic addition with all...
AbstractTask specific ionic liquid as a novel and environmental eco-friendly green catalyst has been...
Activated aryl halides undergo smooth nucleophilic substitution reactions with secondary amines in 1...
A simple, green and environmentally benign procedure was developed for the one pot synthesis of 3-me...
Much attention has been given recently to the use of ionic liquids as highly effective reaction solv...
Heterocycles are the privileged structural subunit of many marketed drug molecules. On the other han...
Alcohols undergo smooth oxidation with iodoxybenzoic acid (IBX) or with Dess-Martin-Periodinane (DMP...
A mild, efficient, and eco-friendly procedure for the conversion of aliphatic, alicyclic and aromati...
Aryl imines, derived in situ from aldehydes and amines, smoothly undergo addition with trimethylsily...
Abstract The epoxides undergo ring-opening reaction smoothly with various amines in an ionic liquid ...
Aziridines undergo ring opening smoothly with various arylamines in 1-butyl-3-methylimidazolium tetr...
One-pot condensation from aromatic aldehyde, methyl ketone, malononitrile and ammonium acetate in th...
AbstractOne-pot condensation from aromatic aldehyde, methyl ketone, malononitrile and ammonium aceta...
Oxiranes undergo ring opening rapidly with sodium azide in a [bmim]BF<SUB>4</SUB>/H<SUB>2</SUB>O or ...
A variety of structurally diverse epoxides undergo facile cleavages by ionic liquid, [AcMIm]X withou...
The imines derived in situ from aldehydes and amines undergo smoothly nucleophilic addition with all...
AbstractTask specific ionic liquid as a novel and environmental eco-friendly green catalyst has been...
Activated aryl halides undergo smooth nucleophilic substitution reactions with secondary amines in 1...
A simple, green and environmentally benign procedure was developed for the one pot synthesis of 3-me...
Much attention has been given recently to the use of ionic liquids as highly effective reaction solv...
Heterocycles are the privileged structural subunit of many marketed drug molecules. On the other han...
Alcohols undergo smooth oxidation with iodoxybenzoic acid (IBX) or with Dess-Martin-Periodinane (DMP...
A mild, efficient, and eco-friendly procedure for the conversion of aliphatic, alicyclic and aromati...
Aryl imines, derived in situ from aldehydes and amines, smoothly undergo addition with trimethylsily...