نتایج جستجو برای: solvent free synthesis

تعداد نتایج: 945899  

Journal: :Archives of Organic and Inorganic Chemical Sciences 2018

E. Abbaspour-Gilandeh S. C. Azimi,

A simple and efficient method for the synthesis of quinolines and polycyclic quinolines using Li+ modified nanoporous Na+-montmorillonite is described. This new nanocatalyst proceeds via Friedlander annulation under solvent-free conditions. It describes our observations about a trend of catalytic activity of Lithium cation in nanoporous Na+-montmorillonite. In this study, several types of 1,3-d...

Journal: :iranian journal of catalysis 2015
khatereh khandan-barani arezo motamedi-asl

for the first time lactic acid was applied as an efficient and green catalyst for the one-pot three-component synthesis of amidoalkyl naphthols via the condensation between arylaldehydes, 2-naphthol and amides or urea under thermal solvent-free conditions in good to excellent yields. we have demonestrated a mild and efficient eco-friendly tandem synthesis of amidoalkyl naphthols using lactic ac...

A. Bamoniri, A. R. Pourali S. M. R. Nazifi

An efficient and environmentally benign   method for the synthesis of aryl iodides have been developed by diazotization of aromatic amines with NaNO2 and nanosilica periodic acid (nano-SPIA) as a green catalyst via grinding followed by a sandmeyer iodination by KI under solvent-free conditions at room temperature. The ensuing aryl diazonium salts supported on nano-SPIA were sufficiently stable ...

Journal: :iranian journal of catalysis 2013
seyyedeh cobra azimi hassan kefayati

a practical and green method for the synthesis of 5h-dibenzo[b,i]xanthene-tetraones and spiro[dibenzo[b,i]xanthene-13,3'-indoline]-pentaones by the condensation of 2-hydroxynaphthalene-1,4-dione with aldehydes or isatins, respectively, in the presence of a catalytic amount of cellulose sulfuric acid (csa) under solvent-free conditions at 100 °c is described. the significant features of this pro...

Journal: :organic chemistry research 0
farzaneh mohamadpour department of chemistry, faculty of science, university of sistan and baluchestan, p. o. box 98135-674 zahedan, iran malek taher maghsoodlu sistan & baluchestan university, zahedan, iran reza heydari department of chemistry, faculty of science, university of sistan and baluchestan, p. o. box 98135-674 zahedan, iran mojtaba lashkari department of chemistry, faculty of science, university of sistan and baluchestan, p. o. box 98135-674 zahedan, iran

an efficient and simple one-pot approach for the synthesis of 3,4-dihydropyrimidin-2-(1h)-one derivatives using antimony trichloride (sbcl3) as a mild catalyst by means of three-component biginelli reaction between β-keto esters, aldehyde derivatives and urea/thiourea under thermal and solvent-free conditions with excellent yields and short reaction times is reported. this methodology offers se...

Faramarz Rostami-Charati Mehdi Shahraki Mohammad R. Hosseini- Tabatabaei Zinatossadat Hossaini

A one-pot synthesis of pyrrole derivatives via reaction between activated carbonyl compounds, primary amines and 1,3-dicarbonyls under solvent-free conditions is described‎.

An efficient sodium bismuthate (NaBiO3) synthesis of biologically active spiro[4H-pyran]derivatives has been accomplished via one-pot three-condensation of isatin/acenaphthequinone, malononitrile and different reagents including 1,3-dicrbonyl compounds, α-naphthol and 4-hydroxycumarin under solvent-free conditions. The notable advantages of the present procedure are: eco-friendly, environmental...

Journal: :international journal of bio-inorganic hybrid nanomaterials 2015
a.s. shahvelayati m. sabbaghan s. banihashem

a simple, green synthesis of n-alkyl-3-acetyl-2-methylpyrrole derivatives using zno nanoparticles from the three component reaction of aliphatic amines, acetylacetone (as a 1,3-dicarbonyl compound) and α-haloketones under solvent-free condition is described.

Faramarz Rostami-Charati Mehdi Shahraki Mohammad R Hosseini- Tabatabaei Zinatossadat Hossaini

one-pot synthesis of pyrrole derivatives via reaction between activated carbonyl compounds, primary amines and 1,3-dicarbonyls under solvent-free conditions is described‎.

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