 
								Synthesis of β-Receptor Blocker and Antihypertensive Drug Using (SBA-Pr-SO3H) as an Eco-Friendly, Inexpensive and Efficient Nano-Catalyst
								
									
										
											
											
												Ali Gharib,
											
										
											
											
												Nader Noroozi Pesyan,
											
										
											
											
												Leila Vojdani Fard,
											
										
											
											
												Mina Roshani
											
										
									
								 
								
									
										Issue:
										Volume 1, Issue 1, April 2015
									
									
										Pages:
										1-5
									
								 
								
									Received:
										10 April 2015
									
									Accepted:
										22 April 2015
									
									Published:
										28 April 2015
									
								 
								
									
										
											
												DOI:
												
												10.11648/j.ajhc.20150101.11
											
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										Abstract: In this method, at first the synthesis of 2,3-dihydro-1H-carbazol-4(9H)-one product by the condensation of (Z)-3-(2-phenylhydrazono)cyclohexanone in the presence of (SBA-Pr-SO3H) as nanoporous solid acid catalyst, acid acetic glacial and ethanol as solvent under reflux conditions is reported. (SBA-Pr-SO3H) nanoporous solid acid catalyst was used as an effective catalyst for the synthesis of Carvedilol from the reaction of 4-oxiranylmethyoxy-9H-carbazole and 2-(2-methoxyphenoxy)ethanamine in the presence of monoglyme solvent. This synthesis afforded under ring opening of 4-oxiranylmethyoxy-9H-carbazole with 2-(2-methoxyphenoxy)ethanamine by above nano-catalyst. Heterogeneous reaction conditions, easy procedure, short reaction time, and high yields are some important advantages of this method.
										Abstract: In this method, at first the synthesis of 2,3-dihydro-1H-carbazol-4(9H)-one product by the condensation of (Z)-3-(2-phenylhydrazono)cyclohexanone in the presence of (SBA-Pr-SO3H) as nanoporous solid acid catalyst, acid acetic glacial and ethanol as solvent under reflux conditions is reported. (SBA-Pr-SO3H) nanoporous solid acid catalyst was used as...
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								Catalytical Synthesis of Pyrazolines Using Nanoparticles of Preyssler Heteropolyacid Supported on Nano-SiO2, H14[NaP5W30O110]/SiO2: A Green and Reusable Catalyst
								
									
										
											
											
												Ali Gharib,
											
										
											
											
												Nader Noroozi Pesyan,
											
										
											
											
												Leila Vojdani Fard,
											
										
											
											
												Mina Roshani
											
										
									
								 
								
									
										Issue:
										Volume 1, Issue 1, April 2015
									
									
										Pages:
										6-12
									
								 
								
									Received:
										10 April 2015
									
									Accepted:
										22 April 2015
									
									Published:
										28 April 2015
									
								 
								
									
										
											
												DOI:
												
												10.11648/j.ajhc.20150101.12
											
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										Abstract: Different Pyrazoline derivatives were synthesized by cyclization of substituted chalcone derivatives in presence of hydrazine hydrate. A series of novel 1,3,5-triaryl pyrazoline derivatives has been synthesized by the reaction of chalcone and phenylhydrazine in the presence of Silica-supported Preyssler Nanoparticles, H14[NaP5W30O110]/SiO2, Preyssler H14[NaP5W30O110] and Keggin heteropolyacids, H3PW12O40, H7[PMo8V4O40], H6[PMo9V3O40], H5[PMo10V2O40], H4[PMo11VO40], H3[PMo12O40] as catalyst under aqueous conditions is described. The best conditions were observed using Preyssler and Silica-supported Preyssler Nanoparticles as catalysts. The catalyst is recyclable and reusable. The structures of compounds obtained were determined by IR and 1H NMR spectra.
										Abstract: Different Pyrazoline derivatives were synthesized by cyclization of substituted chalcone derivatives in presence of hydrazine hydrate. A series of novel 1,3,5-triaryl pyrazoline derivatives has been synthesized by the reaction of chalcone and phenylhydrazine in the presence of Silica-supported Preyssler Nanoparticles, H14[NaP5W30O110]/SiO2, Preyssl...
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								Catalytic Synthesis of 2,3-Diphenylquinoxalines at Room Temperature Using Silica Supported Preyssler Heteropolyacid Catalysts, H14[NaP5W30O110]/SiO2
								
									
										
											
											
												Ali Gharib,
											
										
											
											
												Nader Noroozi Pesyan,
											
										
											
											
												Leila Vojdani Fard,
											
										
											
											
												Mina Roshani
											
										
									
								 
								
									
										Issue:
										Volume 1, Issue 1, April 2015
									
									
										Pages:
										13-20
									
								 
								
									Received:
										10 April 2015
									
									Accepted:
										22 April 2015
									
									Published:
										28 April 2015
									
								 
								
									
										
											
												DOI:
												
												10.11648/j.ajhc.20150101.13
											
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									Abstract: The reaction of Preyssler heteropolyacid, which was used as a catalyst for the room temperature synthesis of quinoxaline derivatives from 1,2-diamino compounds and 1,2-dicarbonyl compounds. The catalyst could be recycled and reused several times without any loss of efficiency.