Add to ORKGThe preparation of 3-oxo-4-azasteroid fromA-nor-3,5-secosteroid-3-oic acid is described in a solventless condition catalysed by Lewis acid under microwave irradiation.We utilized urea as an environmentally benign source for the generation of ammonia for the aza cyclization reaction
AbstractA simple, efficient, and environmentally benign method for a three-component reaction of an ...
1010-1015A straight forward synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones (also called azlacton...
Fourteen azalactones have been synthesized in excellent yields under solvent-free conditions by heat...
A novel catalyst-free synthetic approach to 1,2,3-triazolobenzodiazepinones has been developed and o...
14 Azalactones were synthesized in excellent yields under solvent-free conditions by heating an ald...
The preparation of ring-A fused pyrimidines at the steroidal 2,3-position is herein described. The ...
The preparation of ringA fused pyrimidines at the steroidal 2,3position is herein described. The ...
The synthesis of N-protected 5-oxazolidinones using amino acids, paraformaldehyde and p-toluene sulf...
The synthesis of N-protected 5-oxazolidinones using amino acids, paraformaldehyde and p-toluene sulf...
By direct coupling 7-azaindole and cyclic imines, such as 3,4-dihydroisoquinoline, 6,7-dihydrothieno...
In the present paper, the preparation of 3β-hydroxy-17β-dimethyl- tert-butylsilyloxy-5-azaandrostane...
AbstractWe disclose a new microwave-assisted protocol for the effective α-arylation of diethyl malon...
Silica sulfuric acid, a heterogeneous substance, has been found to be an efficient catalyst for the ...
β-Amino alcohols are important organic compounds with numerous applications. Commonly β-amino alcoho...
The preparation of ring-A fused steroidal dehydropiperazine at the 3,4-position is herein described...
AbstractA simple, efficient, and environmentally benign method for a three-component reaction of an ...
1010-1015A straight forward synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones (also called azlacton...
Fourteen azalactones have been synthesized in excellent yields under solvent-free conditions by heat...
A novel catalyst-free synthetic approach to 1,2,3-triazolobenzodiazepinones has been developed and o...
14 Azalactones were synthesized in excellent yields under solvent-free conditions by heating an ald...
The preparation of ring-A fused pyrimidines at the steroidal 2,3-position is herein described. The ...
The preparation of ringA fused pyrimidines at the steroidal 2,3position is herein described. The ...
The synthesis of N-protected 5-oxazolidinones using amino acids, paraformaldehyde and p-toluene sulf...
The synthesis of N-protected 5-oxazolidinones using amino acids, paraformaldehyde and p-toluene sulf...
By direct coupling 7-azaindole and cyclic imines, such as 3,4-dihydroisoquinoline, 6,7-dihydrothieno...
In the present paper, the preparation of 3β-hydroxy-17β-dimethyl- tert-butylsilyloxy-5-azaandrostane...
AbstractWe disclose a new microwave-assisted protocol for the effective α-arylation of diethyl malon...
Silica sulfuric acid, a heterogeneous substance, has been found to be an efficient catalyst for the ...
β-Amino alcohols are important organic compounds with numerous applications. Commonly β-amino alcoho...
The preparation of ring-A fused steroidal dehydropiperazine at the 3,4-position is herein described...
AbstractA simple, efficient, and environmentally benign method for a three-component reaction of an ...
1010-1015A straight forward synthesis of 4-arylidene-2-phenyl-5(4H)-oxazolones (also called azlacton...
Fourteen azalactones have been synthesized in excellent yields under solvent-free conditions by heat...