A facile one-pot synthesis of 2-aminothiazoles has been carried in PEG-400 as a greener medium at room temperature.This method avoids the use of lachrymatric a-bromoketones as well as the volatile,toxic organic solvents.
A wide range of mono-and disubstituted 2,3-dihydroquinazolin-4（1H）-ones were obtained in high yields by condensation of isatoic anhydride,aldehydes with ammonium salts or primary amines in the presence of strontium ...A wide range of mono-and disubstituted 2,3-dihydroquinazolin-4（1H）-ones were obtained in high yields by condensation of isatoic anhydride,aldehydes with ammonium salts or primary amines in the presence of strontium chloride in aqueous ethanol under reflux.展开更多
This paper describes the combustion synthesis ofα-Fe2O3 nanopowder at much lower temperature and its catalytic activity for the one-pot preparation of 3,4-dihydropyrano[c]chromenes.The combustion derivedα-Fe_2O_3 na...This paper describes the combustion synthesis ofα-Fe2O3 nanopowder at much lower temperature and its catalytic activity for the one-pot preparation of 3,4-dihydropyrano[c]chromenes.The combustion derivedα-Fe_2O_3 nanopowder was characterized by powder X-ray diffraction（PXRD）,Braunauer,Emmett and Teller（BET） surface area,scanning electron microscopy（SEM） and Fourier transform infrared spectroscopy（FTIR）.Highly efficient,three-component condensation of aromatic aldehyde,malanonitrile and 4- hydroxycoumarin catalyzed byα-Fe2O3 nanoparticles at room temperature is described.The method offers an excellent alternative to the synthesis of 3,4-dihydropyrano[c]chromenes.The reactions are rapid,clean,and the products with good yield and high purity.展开更多
Disubstituted oxazoles were prepared conveniently by treatment of aromatic -methyl ketones and nitriles with poly[styrene(iodosodiacetate)] in one-pot process.
An efficient one-pot synthetic protocol was developed for the synthesis of imidazo[ 1,2-a]pyridines from easily available starting materials： Aromatic ketones, α/βunsaturated ketones,β-keto esters and 2- aminopyri...An efficient one-pot synthetic protocol was developed for the synthesis of imidazo[ 1,2-a]pyridines from easily available starting materials： Aromatic ketones, α/βunsaturated ketones,β-keto esters and 2- aminopyridines. The present reaction proceeded well in MeOH under the media of I2/CuO. By using this method, the marketed drug zolimidine could be prepared easily with 95% yield. All these target products were characterized by NMR, HRMS and IR spectra. Furthermore, the target compound 3fa was determined bv X-ray crystallographic analysis.展开更多
A mild, one-pot procedure for the synthesis of vinyl ethers in good yields from 2-hydroxyalkyl phenyl selenides with primary or secondary organic halides has been developed.
A convenient one-pot synthesis of functionalized （E）-2-arylvinyl bromides was achieved by microwave-induced deacetylation and subsequent acylation using dicyclohexyl carbodiimide （DCC） and dimethylamino-pyridine ...A convenient one-pot synthesis of functionalized （E）-2-arylvinyl bromides was achieved by microwave-induced deacetylation and subsequent acylation using dicyclohexyl carbodiimide （DCC） and dimethylamino-pyridine （DMAP） at room temperature from （E）-4-（2-bromovinyl）phenyl acetate.展开更多
N-Boc-2, 5-bis(trimethylsilyl)pyrrolidine 4 was synthesized from the reaction of N-Boc-pyrrolidine 1 with trimethylsilyl chloride (TMSCl) at optional temperature in one-pot in good yield.
A one-pot sequential reaction for efficient synthesis of pyrrolo[2,1-a]isoquinoline and pyrrolo[1,2-a]quinoline derivatives has been developed.The reaction included firstly the Cu-catalyzed three-component reaction of...A one-pot sequential reaction for efficient synthesis of pyrrolo[2,1-a]isoquinoline and pyrrolo[1,2-a]quinoline derivatives has been developed.The reaction included firstly the Cu-catalyzed three-component reaction of isoquinoline（quinoline）,acetylenedicarboxylate and alkynylbenzene and then Cs 2 CO 3-promoted intramolecular cyclization reaction of initially formed 1-alkenyl-2-alkynyl-1,2-dihydroisoquinoline（1,2-dihydroquinoline）.展开更多
Pyridinone derivatives are of great interest in medicinal chemistry where they were found to be potent to various diseases. Their metal complexes added more value to their applications. Here, we have synthesized two 2...Pyridinone derivatives are of great interest in medicinal chemistry where they were found to be potent to various diseases. Their metal complexes added more value to their applications. Here, we have synthesized two 2-pyridinone derivatives(3-cyano-4-(4-hydroxy-3-methoxyphenyl)-6-phenyl-2(1 H)-pyridinone and 3-cyano-4-chlorophenyl-6-(4-tolyl)-2(1 H)-pyridinone) using one-pot multicomponent system. They were well characterized using spectroscopic techniques like nuclear magnetic resonance(NMR-1 H & 13 C), Fourier transform infrared(FT-IR) and UV/Vis spectroscopy. The final structures were determined using single-crystal X-ray diffraction technique which helps us to determine their geometries. Density functional theory(DFT) and time-dependent density functional theory(TD-DFT) with suitable basis-sets of calculations have correctly simulated these spectroscopic parameters. The intramolecular charge transfer(ICT) of both substrates has been discussed using natural bond orbital(NBO) technique. Molecular electrostatic potential(MEP) surfaces showed their reactive locations for intermolecular charge transfer. Compared to p-nitroaniline(pNA), both substrates were shown to have substantial molecular hyperpolarizability.展开更多
A one-pot synthesis of 2-（1-acyloxypcntyl） benzoic acids by trapping the carboxylatc/alkoxide dianion with acylating reagents following Grignard addition with n-BuMgBr to 2-formylbcnzoic acid was described. Compared...A one-pot synthesis of 2-（1-acyloxypcntyl） benzoic acids by trapping the carboxylatc/alkoxide dianion with acylating reagents following Grignard addition with n-BuMgBr to 2-formylbcnzoic acid was described. Compared with routine synthetic method, this novel procedure has the advantage of convenient operation and higher yields.展开更多
New 9-（alkyl or aryl）acenaphtho[l,2-b]furan-8-（alky or aryl）amine compounds has herein been reported by one-pot reaction of （acenaphthylen-l-yloxy）trimethylsilane,alkyl and aryl aldehydes,and aryl and alky isocy...New 9-（alkyl or aryl）acenaphtho[l,2-b]furan-8-（alky or aryl）amine compounds has herein been reported by one-pot reaction of （acenaphthylen-l-yloxy）trimethylsilane,alkyl and aryl aldehydes,and aryl and alky isocyanides in refluxing DMF.展开更多
文摘A facile one-pot synthesis of 2-aminothiazoles has been carried in PEG-400 as a greener medium at room temperature.This method avoids the use of lachrymatric a-bromoketones as well as the volatile,toxic organic solvents.
文摘A wide range of mono-and disubstituted 2,3-dihydroquinazolin-4（1H）-ones were obtained in high yields by condensation of isatoic anhydride,aldehydes with ammonium salts or primary amines in the presence of strontium chloride in aqueous ethanol under reflux.
基金VTU(VTU/Aca./2009-10/A-9/11714) for the financial support and Chemistry-TEQIP Laboratory of MSRIT and SSMRV College, Chemistry Research Center
文摘This paper describes the combustion synthesis ofα-Fe2O3 nanopowder at much lower temperature and its catalytic activity for the one-pot preparation of 3,4-dihydropyrano[c]chromenes.The combustion derivedα-Fe_2O_3 nanopowder was characterized by powder X-ray diffraction（PXRD）,Braunauer,Emmett and Teller（BET） surface area,scanning electron microscopy（SEM） and Fourier transform infrared spectroscopy（FTIR）.Highly efficient,three-component condensation of aromatic aldehyde,malanonitrile and 4- hydroxycoumarin catalyzed byα-Fe2O3 nanoparticles at room temperature is described.The method offers an excellent alternative to the synthesis of 3,4-dihydropyrano[c]chromenes.The reactions are rapid,clean,and the products with good yield and high purity.
文摘Disubstituted oxazoles were prepared conveniently by treatment of aromatic -methyl ketones and nitriles with poly[styrene(iodosodiacetate)] in one-pot process.
基金the National Natural Science Foundation of China (Nos. 21032001 and 21272085) for their generous financial supportthe excellent doctorial dissertation cultivation grant from Central China Normal University Wuhan, China (No. 2013YBYB63)
文摘An efficient one-pot synthetic protocol was developed for the synthesis of imidazo[ 1,2-a]pyridines from easily available starting materials： Aromatic ketones, α/βunsaturated ketones,β-keto esters and 2- aminopyridines. The present reaction proceeded well in MeOH under the media of I2/CuO. By using this method, the marketed drug zolimidine could be prepared easily with 95% yield. All these target products were characterized by NMR, HRMS and IR spectra. Furthermore, the target compound 3fa was determined bv X-ray crystallographic analysis.
基金the Natural Science Foundation of Jiangxi Province(No.0420017)for financial support
文摘A mild, one-pot procedure for the synthesis of vinyl ethers in good yields from 2-hydroxyalkyl phenyl selenides with primary or secondary organic halides has been developed.
基金supported by the Natural Science Foundation of Shanghai,China(No.06ZR14085)the Scientific Research Foundation for the Returned Overseas Chinese Scholars,State Education Ministry.
文摘A convenient one-pot synthesis of functionalized （E）-2-arylvinyl bromides was achieved by microwave-induced deacetylation and subsequent acylation using dicyclohexyl carbodiimide （DCC） and dimethylamino-pyridine （DMAP） at room temperature from （E）-4-（2-bromovinyl）phenyl acetate.
基金the National Natural Science Foundation of China (No 29772004).
文摘N-Boc-2, 5-bis(trimethylsilyl)pyrrolidine 4 was synthesized from the reaction of N-Boc-pyrrolidine 1 with trimethylsilyl chloride (TMSCl) at optional temperature in one-pot in good yield.
基金Supported by the National Natural Science Foundation of China(No.21172189)
文摘A one-pot sequential reaction for efficient synthesis of pyrrolo[2,1-a]isoquinoline and pyrrolo[1,2-a]quinoline derivatives has been developed.The reaction included firstly the Cu-catalyzed three-component reaction of isoquinoline（quinoline）,acetylenedicarboxylate and alkynylbenzene and then Cs 2 CO 3-promoted intramolecular cyclization reaction of initially formed 1-alkenyl-2-alkynyl-1,2-dihydroisoquinoline（1,2-dihydroquinoline）.
文摘Pyridinone derivatives are of great interest in medicinal chemistry where they were found to be potent to various diseases. Their metal complexes added more value to their applications. Here, we have synthesized two 2-pyridinone derivatives(3-cyano-4-(4-hydroxy-3-methoxyphenyl)-6-phenyl-2(1 H)-pyridinone and 3-cyano-4-chlorophenyl-6-(4-tolyl)-2(1 H)-pyridinone) using one-pot multicomponent system. They were well characterized using spectroscopic techniques like nuclear magnetic resonance(NMR-1 H & 13 C), Fourier transform infrared(FT-IR) and UV/Vis spectroscopy. The final structures were determined using single-crystal X-ray diffraction technique which helps us to determine their geometries. Density functional theory(DFT) and time-dependent density functional theory(TD-DFT) with suitable basis-sets of calculations have correctly simulated these spectroscopic parameters. The intramolecular charge transfer(ICT) of both substrates has been discussed using natural bond orbital(NBO) technique. Molecular electrostatic potential(MEP) surfaces showed their reactive locations for intermolecular charge transfer. Compared to p-nitroaniline(pNA), both substrates were shown to have substantial molecular hyperpolarizability.
文摘A one-pot synthesis of 2-（1-acyloxypcntyl） benzoic acids by trapping the carboxylatc/alkoxide dianion with acylating reagents following Grignard addition with n-BuMgBr to 2-formylbcnzoic acid was described. Compared with routine synthetic method, this novel procedure has the advantage of convenient operation and higher yields.
文摘New 9-（alkyl or aryl）acenaphtho[l,2-b]furan-8-（alky or aryl）amine compounds has herein been reported by one-pot reaction of （acenaphthylen-l-yloxy）trimethylsilane,alkyl and aryl aldehydes,and aryl and alky isocyanides in refluxing DMF.
