Heterocycles are the privileged structural subunit of many marketed drug molecules. On the other hand, the last decade has seen tremendous applications of the ionic liquid [bmim]PF6 (1-butyl-3-methyl-1H-imidazolium hexafluorophosphate) as an efficient, cheap, commercially available, low toxic reaction medium for various organic transformations. The present review summarizes recent reported applications of [bmim]PF6 as an efficient reaction medium for the synthesis of diverse biologically relevant heterocycles
The combination of isatins, active methylene reagents and 4-phenylurazole/ phthalhydrazide in the pr...
[[abstract]]A mild and efficient route for the synthesis of quinolines and polycyclic quinolines uti...
Activated aryl halides undergo smooth nucleophilic substitution reactions with secondary amines in 1...
Much attention has been given recently to the use of ionic liquids as highly effective reaction solv...
The synthesis of heterocycles is a prominent feature of organic chemistry, due to the enormous impor...
Epoxides undergo smooth ring-opening with aryl amines in 1-butyl-3-methylimidazolium tetrafluorobora...
The imines derived in situ from aldehydes and amines undergo smoothly nucleophilic addition with all...
A simple, green and environmentally benign procedure was developed for the one pot synthesis of 3-me...
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...
In this paper we report examples of the Heck reaction in the new moisture stable ambient temperature...
This research project is concerned with the development and use of eco-friendly reaction media for a...
The room temperature ionic liquid [bmim][PF 6] has been demonstrated to be an efficient and recyclab...
Eco-friendly synthesis of some selected Barbiturates, Thiobarbiturates and Dimedone derivatives has ...
Aziridines undergo ring opening smoothly with various arylamines in 1-butyl-3-methylimidazolium tetr...
The combination of isatins, active methylene reagents and 4-phenylurazole/ phthalhydrazide in the pr...
[[abstract]]A mild and efficient route for the synthesis of quinolines and polycyclic quinolines uti...
Activated aryl halides undergo smooth nucleophilic substitution reactions with secondary amines in 1...
Much attention has been given recently to the use of ionic liquids as highly effective reaction solv...
The synthesis of heterocycles is a prominent feature of organic chemistry, due to the enormous impor...
Epoxides undergo smooth ring-opening with aryl amines in 1-butyl-3-methylimidazolium tetrafluorobora...
The imines derived in situ from aldehydes and amines undergo smoothly nucleophilic addition with all...
A simple, green and environmentally benign procedure was developed for the one pot synthesis of 3-me...
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...
In this paper we report examples of the Heck reaction in the new moisture stable ambient temperature...
This research project is concerned with the development and use of eco-friendly reaction media for a...
The room temperature ionic liquid [bmim][PF 6] has been demonstrated to be an efficient and recyclab...
Eco-friendly synthesis of some selected Barbiturates, Thiobarbiturates and Dimedone derivatives has ...
Aziridines undergo ring opening smoothly with various arylamines in 1-butyl-3-methylimidazolium tetr...
The combination of isatins, active methylene reagents and 4-phenylurazole/ phthalhydrazide in the pr...
[[abstract]]A mild and efficient route for the synthesis of quinolines and polycyclic quinolines uti...
Activated aryl halides undergo smooth nucleophilic substitution reactions with secondary amines in 1...