Microwave-induced fast addition of several amines to conjugated carbonyl compounds has been carried out in water very efficiently in the absence of any catalyst
Department of Applied Chemistry, Banaras Hindu University, Varanasi-221 005, Uttar Pradesh, lndia E-...
A simple and efficient protocol has been developed for the direct synthesis of γ-nitrobutyric acid m...
Microwave-mediated chemistry, involving the reduction of nitroarenes with molybdenum hexacarbonyl as...
Microwave-induced fast addition of several amines to conjugated carbonyl compounds has been carried ...
The addition of amines to conjugated alkenes has been carried out in water at room temperature very ...
C-C bond formation via Michael addition is achieved in high yields and short times by employing cata...
825-828A simple and efficient protocol has been developed for the aza-Michael addition of amines to ...
An efficient entry to aromatic amides using microwave irradiation in aqueous medium is described. St...
An efficient entry to aromatic amides using microwave irradiation in aqueous medium is described. St...
For the first time the unimolecular Newman–Kwart rearrangement is performed in pure water. The eleva...
A series of Michael adducts (5-11) have been synthesized with good yields under solvent-free microwa...
Michael addition of aldehydes and ketones to trans-nitrostyrene catalyzed by L-proline was investiga...
A simple and efficient protocol has been developed for the Michael addition ofamines to α,β-unsatura...
Acombination ofwater and microwave irradiationwas used for the first timeto performa catalyst-free n...
A novel and efficient synthesis of N-arylamines by the reaction of activated aryl halides with secon...
Department of Applied Chemistry, Banaras Hindu University, Varanasi-221 005, Uttar Pradesh, lndia E-...
A simple and efficient protocol has been developed for the direct synthesis of γ-nitrobutyric acid m...
Microwave-mediated chemistry, involving the reduction of nitroarenes with molybdenum hexacarbonyl as...
Microwave-induced fast addition of several amines to conjugated carbonyl compounds has been carried ...
The addition of amines to conjugated alkenes has been carried out in water at room temperature very ...
C-C bond formation via Michael addition is achieved in high yields and short times by employing cata...
825-828A simple and efficient protocol has been developed for the aza-Michael addition of amines to ...
An efficient entry to aromatic amides using microwave irradiation in aqueous medium is described. St...
An efficient entry to aromatic amides using microwave irradiation in aqueous medium is described. St...
For the first time the unimolecular Newman–Kwart rearrangement is performed in pure water. The eleva...
A series of Michael adducts (5-11) have been synthesized with good yields under solvent-free microwa...
Michael addition of aldehydes and ketones to trans-nitrostyrene catalyzed by L-proline was investiga...
A simple and efficient protocol has been developed for the Michael addition ofamines to α,β-unsatura...
Acombination ofwater and microwave irradiationwas used for the first timeto performa catalyst-free n...
A novel and efficient synthesis of N-arylamines by the reaction of activated aryl halides with secon...
Department of Applied Chemistry, Banaras Hindu University, Varanasi-221 005, Uttar Pradesh, lndia E-...
A simple and efficient protocol has been developed for the direct synthesis of γ-nitrobutyric acid m...
Microwave-mediated chemistry, involving the reduction of nitroarenes with molybdenum hexacarbonyl as...
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