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1.
Fe3O4 magnetic nanoparticles were synthesized and functionalized by propylsilan and after that arginine. The synthesized Fe3O4@PS-Arginine magnetic nanoparticles were modified to obtain Fe3O4@PS-Arg[HSO4]. These nanoparticles were used as environmental friendly solidacid magnetic nanocatalyst for the synthesis of 2-amino-4-arylbenzo[h]quinoline-3-carbonitrile and 10,10-dimethyl-7-aryl-9,10,11,12-tetrahydrobenzo[c]acridin-8(7H)-one derivatives via the one-pot reaction of α-naphthilamine and aromatic aldehydes with malononitrile or dimedone. Simple operation, high reaction yields, reusability of catalyst for several times, short reaction time and easy separation from reaction mixture are the key advantages of using this catalyst.  相似文献   

2.
The conversion of soluble polyoxometalate into insoluble polyoxometalate is considered to be one of the major challenges in synthetic organic chemistry. Here, polyoxometalate was bonded to the salt part of an organic branch immobilized on the silica-coated Fe3O4 nanoparticle and characterized using various techniques. The fabricated complex was used as a heterogeneous catalyst in a novel one-pot reaction for synthesis of benzo[4,5]imidazo[1,2-a]pyrimidin-2-ones using aromatic amines, dimethyl acetylenedicarboxylate (DMAD), derivatives of benzaldehyde and 2-aminobenzimidazole in water/ethanol as a green solvent. 21 derivatives of benzo[4,5]imidazo[1,2-a]pyrimidin-2-one were synthesized by this method and fully characterized. The high stability of the catalyst showed that it can be reused for 6 times without decreasing in activity. The combination of new synthetic method, new ferromagnetic heterogeneous nano-catalyst, green solvent and simple separation method were presented in this work.  相似文献   

3.
A simple, economical, three-component, and one-pot synthesis of novels spiro[indoline-3,5′-pyrido[2,3-d]pyrimidine] derivatives by condensation of dimethyl acetylene dicarboxylate, isatin derivatives, and 6-amino-1,3-dimethyluracil in presence of Fe3O4@Propylsilane@Histidine[HSO4] as an impressive catalyst via reflux and ultrasound procedure is described. The results show that ultrasound method has several advantages such as milder condition, shorter reaction time, and higher reaction yield.  相似文献   

4.
Ezhumalai Yamuna 《合成通讯》2014,44(18):2656-2661
A facile, efficient, and environmentally friendly protocol for the synthesis of pyrano[2,3-a]carbazoles has been developed by one-pot multicomponent reaction of benzaldehyde/isatin with malononitrile and 1-hydroxycarbazoles in the presence of InCl3 as catalyst.  相似文献   

5.
Abstract

An efficient one-pot synthesis of 1?H-indazolo[1,2-b]phthalazine-trione and spiro-triazolo[1,2-a]indazole-tetraone derivatives via three-component condensation reaction of phthalhydrazide or 4-phenylurazole, aldehydes or isatins and dimedone in the presence of a catalytic amount of silica-supported tungstic acid (STA), as a heterogeneous solid acid catalyst under solvent-free conditions is presented. This ecofriendly protocol offers several advantages such as a cost-effective procedure with excellent yields, short reaction time, simple workup, recovery and reusability of catalyst with broad scope of usable substrates. This has made the protocol sustainable and economic.  相似文献   

6.
In this study, poly(2-ethyl-2-oxazoline) (PEtOx) immobilized on Fe3O4 nanoparticles (Fe3O4@SiO2/PEtOx) has been constructed as a new, heterogeneous, efficient, and recyclable nanocatalyst. The prepared nanocatalyst was characterized by Fourier transform infrared (FTIR), scanning electron microscopy (SEM), powder X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS) analysis, and vibrating-sample magnetometer (VSM) techniques. Nanocatalyst was employed to synthesize benzo[b]xanthene-triones and tetrahydrochromeno[2,3-b]xanthene tetraones via one-pot three- or pseudo–five-component reaction between 2-hydroxy-1,4-naphthoquinone or 2,5-dihydroxy-1,4-benzoquinone, aldehyde, and dimedone or 1,3-cyclohexanedione under reflux condition in ethanol. The catalyst could be easily separated and recycled several times without considerable loss of activity. Clean methodology, easy work-up, mild reaction condition, short reaction time with good-to-excellent yields, and simple preparation of the catalyst are some advantages of the presented work.  相似文献   

7.

One-pot three-component synthesis of twelve different chromeno[2,3-b]indole derivatives were achieved by the condensation of β-naphthol, oxindole and various substituted aldehydes. Two more chromeno[2,3-b]indole derivatives were also synthesized through one-pot two-component condensation of salicylaldehyde with oxindole/chlorooxindole. Both the condensations were achieved by using Keggin-type heteropoly-11-molybdo-1-vanadophosphoric acid, H4[PVMo11O40] supported on montmorillonite K-10 clay for about 10% as catalyst under environmentally benign solvent-free reaction condition. Shorter reaction time, excellent yield of product, sustainability of catalytic material and simple workup procedure under green experimental conditions are the advantages of this protocol.

  相似文献   

8.
Abstract

An efficient solvent-free access towards highly substituted pyrido[2′,3′:3,4]pyrazolo[1,5-a]pyrimidine-3-carbonitrile derivatives has been established through multi-component reaction of 1H‐pyrazolo[3,4‐b]pyridin‐3‐amine, aldehyde, 3-(1H-indol-3-yl)-3-oxopropanenitrile catalyzed by 1,1,3,3-tetramethylguanidine (TMG). The reaction allows the formation of one C?C and two C?N bonds with high yield. The significant features of this solvent-free reaction include mild reaction condition, readily accessible substrates, short reaction time, excellent yield, and broad substrate scopes as well as simple one-pot operation, no column chromatographic purification, which makes this strategy highly attractive.  相似文献   

9.
A series of novel pyrimido[4,5-c]isoquinolines (3a–3h) and 1,2,3-triazole-coupled pyrimido[4,5-c]isoquinolines (4a–4h) were synthesized in good to excellent yields in the one-pot method. The reaction of 6-amino-1,3-dimethyluracil with different 2-iodo benzoyl chlorides using Pd catalyst in dimethylformamide afforded corresponding pyrimido[4,5-c]isoquinolines (3a–3h). One-pot reaction of pyrimido[4,5-c]isoquinolines with propargyl bromide and benzyl azide in THF at room temperature furnished 1,2,3-triazole-coupled pyrimido[4,5-c]isoquinoline (4a–4h). In vitro antioxidant activity examination revealed that compounds 4d and 4c found to exhibit potent antioxidant activity as compared to the standard drug Trolox with IC50 values 6.02?±?0.6 and 12.18?±?0.9?µM, respectively.  相似文献   

10.
Indium(III) chloride catalyzed one-pot synthesis of 12-aryl/alkyl-8,9,10,12-tetrahydrobenzo[a]xanthene-11-one and 8,10-dimethyl-12-aryl-8,12-dihydro-7-oxa-8,10-diazabenzo[a]anthracene-9,11-dione derivatives have been achieved by three component cyclocondensation of aldehydes, β-naphthol and cyclic 1,3-dicarbonyl compounds under solvent free condition in high yields. P2O5 too has been found as an effective catalyst towards this transformation.  相似文献   

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