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    The efficient synthesis of carbon–carbon double bonds via Knoevenagel condensation using red mud packed in a column

    , Article Green Chemistry Letters and Reviews ; Volume 1, Issue 1 , 2007 , Pages 61-64 ; 17518253 (ISSN) Khezri, S. H ; Mohammad Vali, M ; Eftekhari Sis, B ; Mahmoodi Hashemi, M ; Baniasadi, M. H ; Sharif University of Technology
    2007
    Abstract
    Red mud (RM) is generated as a by-product during the production of alumina from bauxite ore. In this study, RM packing in a column is used as a catalyst for carbon–carbon double bond formation via Knoevenagel condensation. The reactants are added to the top of the column and then eluted with solvent. The products are collected in high yields and short time. RM packed in a column eliminates a catalyst separation step from the reaction mixture in this work. © 2007 Taylor & Francis Group, LLC  

    Synthesis of Green Catalyst Based on Starch and its Application in Knovenagel Reaction

    , M.Sc. Thesis Sharif University of Technology Nikooseresht, Navid (Author) ; Pourjavadi, Ali (Supervisor)
    Abstract
    Polysaccharide is important in terms of their environmental interest, scientists have been growing. According to the structural properties of this interesting class of natural polymers, in terms of having chemically active groups on the high density polymer housing provides the possibility That can perform chemical reactions with the new properties of these polymers to give. Starch polysaccharides in the project through a chemical reaction to the structure of a third type of bridge Amen to that using 1HNMR and 13CNMR predicted structure was approved. The modified polysaccharide has catalyst activity. This activity in knovenagel reaction for some aldhydes was used and results were... 

    Synthesis of Rhodanine-Oxindole Derivatives by Using Multi-Component Reactions in Green Solvent

    , M.Sc. Thesis Sharif University of Technology Jalalinik, Mahbod (Author) ; Matloubi Moghaddam, Firouz (Supervisor)
    Abstract
    Nowadays, heterocyclic compounds have become extremely important in various industries, especially the pharmaceutical industry.In this project, an efficient and environmentally friendly path is presented to synthesize numerous rhodanine-oxindole derivatives in polyethylene Glycol in one pot-four components procedure. This pathway doesn't need harsh reaction conditions such as high temperature, long time, catalysts, complicated separation steps, toxic solvents, etc. all products have been made under green strategy with high yield.
     

    Synthesis of Heterocyclic Compounds via Domino Knoevenagel Hetero Diels–Alder Reaction on Thiocarbonyls and Investigation of Tandem Dinucleophilic Addition on Pyridinium Salts

    , Ph.D. Dissertation Sharif University of Technology Kiamehr, Mostafa (Author) ; Matloubi Moghaddam, Firouz (Supervisor)
    Abstract
    In the first chapter, three efficient synthesis of novel polyheterocyclic indole and thiochromone-annulated thiopyranocoumarin derivatives are achieved via domino Knoevenagel hetero Diels–Alder reaction of O-acrylated and O-propargylated salicylaldehyde derivatives with indolin-2-thiones and 4-hydroxy dithiocoumarin. The domino Knoevenagel-hetero-Diels–Alder reactions are very efficient process that allows the formation of two or more rings at once, avoiding sequential chemical transformations. The products are formed in good-to-excellent yields with high regio- and stereoselectivity. The major advantage of this reaction is the ease of the work-up during which the products can be isolated... 

    Synthesis of Thiopyrano Indole Annulated Benzo -δ-Sultones Via Domino Knoevenagele Hetero-Dielse Alder Reaction& Synthesis of Dispiro Compounds Via On-Pot Three Componet 1,3- Dipolar Cycloaddition

    , M.Sc. Thesis Sharif University of Technology Qahremannjad, Zahra (Author) ; Moghaddam, Matloubi (Supervisor)
    Abstract
    The domino-Knoevenagele hetero-Dielse Alder reaction is an efficient synthesis of complex compounds like natural products from simple substrates and highly diverse molecules. In the first chapter, synthesis of pyran, pyranopyran, pyrano-thiopyran heterocycles and [6,5] pyranopyrrole derivatives are achieved via domino Knoevenagele hetero-Dielse Alder reaction of O-acrylated and o- propargylated salicylaldehyde derivatives with thiooxindole and 4- hydroxyl dithiocoumarin. We discovered a new and efficient synthesis of a great variety of thiopyrano indole annulated benzo -δ-sultones via domino Knoevenagele hetero-Dielse Alder reaction of thiooxindole derivatives and (E)-2-formylphenyl... 

    Use of Suitable Methods in Synthesis of Spiropyrrolididne Oxindole, Polysubstituted Thiophene, Thiopyrano Benzosultone and Pyrimidines by Cycloaddition Reactions

    , Ph.D. Dissertation Sharif University of Technology Khodabakhshi, Mohammad Reza (Author) ; Matloubi Moghaddam, Firouz (Supervisor)
    Abstract
    We have reported a new and efficient synthesis of a broad spectrum of heterotetracyclic thiopyranoindole via knovenagel hetero diels alder reaction.Fused pyrimidines have attracted considerable attention in synthetic organic chemistry because of their wide range of biological activities pharmaceutical and therapeutic properties, and antibacterial, antiviral, antitumor, and anti-inflammatory activities. We have reported a new efficient method for synthesis of pyrimidines fused to coumarine, uracile, cyclohexane and triamino pyrimidine structures. The major benefits of the current study are high yields, short reaction times, mild reaction conditions and available materials..We have also... 

    Synthesis of soluble N-functionalized polysaccharide derivatives using phenyl carbonate precursor and their application as catalysts

    , Article Starch/Staerke ; Volume 63, Issue 12 , 2011 , Pages 780-791 ; 00389056 (ISSN) Pourjavadi, A ; Seidi, F ; Afjeh, S. S ; Nikoseresht, N ; Salimi, H ; Nemati, N ; Sharif University of Technology
    2011
    Abstract
    Soluble N-functionalized basic and cationic polysaccharides have been synthesized using polysaccharide phenyl carbonate as a precursor. The products and intermediates were thoroughly characterized by conventional methods. The quaternization of amino intermediates in various conditions was studied. Moreover, the potential of basic polymers as green and selective catalysts in Knoevenagel reaction was investigated. In all cases, only one isomer was obtained  

    Designing a New Ligand based on Pyridine for Immobilization of Gold Nanoparticles on Reduced Magnetic Graphene Oxide: A New Catalyst for the Reduction of Nitro Compounds and a Diastereoselective Construction of Functionalized Dihydro-Pyridazine based Spirooxindole Scaffold via C-3 Umpolung of Isatin N,N′-Cyclic Azomethine Imine

    , M.Sc. Thesis Sharif University of Technology Siahpoosh, Ali (Author) ; Matloubi Moghadam, Firouz (Supervisor)
    Abstract
    In this work, a new catalyst based on gold nanoparticles immobilized on magnetic GO (graphene oxide) has been introduced. A new ligand based on pyridine has been used to the functionalization of GO to design robust heterogeneous catalyst for reduction in a short time using a low amount of the catalyst. The prepared catalyst was employed in the synthesis of aromatic amines using various types of nitroarnes in water. This catalyst is readily prepared from available starting materials and also is a reusable catalyst having very good stability to air and moisture. The proposed procedure applied here can conduct the reactions under milder reactions. Finally, due to total removal of the... 

    Facile synthesis of highly substituted 2-pyrone derivatives via a tandem Knoevenagel condensation/lactonization reaction of β-formyl-esters and 1,3-cyclohexadiones

    , Article Tetrahedron Letters ; Vol. 55, issue. 18 , April , 2014 , p. 2908-2911 ; ISSN: 00404039 Moghaddam, F. M ; Mirjafary, Z ; Javan, M. J ; Motamen, S ; Saeidian, H ; Sharif University of Technology
    Abstract
    A mild and efficient tandem process for the synthesis of new highly substituted 2-pyrones starting from commercially available 2-arylacetic acids has been developed. The synthesis is based on the Knoevenagel condensation of 1,3-cyclohexadiones with various β-formyl-esters, followed by lactonization in the presence of nano ZnO (20 mol %). Moderate to high yields and readily available cheap starting materials are the key features of the present method  

    An efficient ZnO-catalyzed synthesis of novel indole-annulated thiopyrano-chromene derivatives via Domino Knoevenagel-hetero-Diels-Alder reaction

    , Article Tetrahedron Letters ; Volume 50, Issue 48 , 2009 , Pages 6723-6727 ; 00404039 (ISSN) Kiamehr, M ; Matloubi Moghaddam, F ; Sharif University of Technology
    Abstract
    An efficient synthesis of pentacyclic indole derivatives is achieved via domino Knoevenagel-hetero-Diels-Alder reactions of indolin-2-thiones and O-propargylated salicylaldehyde derivatives in CH3CN in the presence of 10 mol % of ZnO as a heterogeneous catalyst. The products are formed in good to excellent yields  

    Synthesis of novel pentacyclic thiopyrano indole-annulated benzo-δ-sultone derivatives via a domino Knoevenagel-hetero-Diels-Alder reaction in water

    , Article Tetrahedron Letters ; Volume 54, Issue 21 , 2013 , Pages 2685-2689 ; 00404039 (ISSN) Moghaddam, F. M ; Khodabakhshi, M. R ; Kiamehr, M ; Ghahremannejad, Z ; Sharif University of Technology
    2013
    Abstract
    An efficient synthesis of novel pentacyclic thiopyrano indole-annulated benzo-δ-sultone derivatives is achieved via intramolecular domino Knoevenagel-hetero-Diels-Alder reaction of 2-formylphenyl (E)-2-phenylethenyl sulfonates and indoline-2-thiones in aqueous medium. The products are formed in good yields with high regio- and stereoselectivity  

    Tungstate-loaded triazine-based magnetic poly(Bis-imidazolium ionic liquid): An effective bi-functional catalyst for tandem selective oxidation/Knoevenagel condensation in water

    , Article Polymer (United Kingdom) ; Volume 112 , 2017 , Pages 342-350 ; 00323861 (ISSN) Zohreh, N ; Tavakolizadeh, M ; Hosseini, S. H ; Pourjavadi, A ; Bennett, C ; Sharif University of Technology
    Elsevier Ltd  2017
    Abstract
    A novel bi-functional polymeric catalyst was synthesized by immobilization of tungstate anions onto the nitrogen rich poly(ionic liquid)/magnetic nanocomposite. The resulting catalyst has two types of catalytic sites: (i) immobilized WO4 anions with bis-imidazolium ionic liquid cation for selective oxidation of alcohols and (ii) basic amine groups for Knoevenagel condensation between produced aldehyde and malononitrile. Due to the polymeric nature of the catalyst, large amounts of tungstate and basic nitrogen groups were presented on the solid surface which led to a decrease in the applied catalyst mass for catalytic reaction. High catalytic activity and excellent selectivity of catalyst in... 

    Microwave-assisted synthesis of 3-substituted coumarins using ZrOCl 2.8H2O as an effective catalyst

    , Article Scientia Iranica ; Volume 16, Issue 1 C , 2009 , Pages 12-16 ; 10263098 (ISSN) Matloubi Moghaddam, F ; Mirjafary, Z ; Saeidian, H ; Sharif University of Technology
    2009
    Abstract
    An efficient route for the synthesis of 3-substituted coumarins via Knoevenagel condensation, using ZrOCl2.8H2O (10 mol %) as the. catalyst under microwave heating and solvent-free conditions, is described. This procedure offers several advantages, including the low loading of catalysts, high yields, clean reactions, short reaction times and the. use of various substrates, which make it a useful and attractive strategy for the. synthesis of 3-substituted coumarins. © Sharif University of Technology, June 2009  

    Diastereo- and enantioselective synthesis of α,β-disubstituted γ-nisalkoxycarbonyl sulfonates

    , Article Synlett ; Issue 17 , 2009 , Pages 2872-2874 ; 09365214 (ISSN) Enders, D ; Saeidian, H ; Mirjafary, Z ; Iffland, D ; Raabe, G ; Runsink, J ; Sharif University of Technology
    2009
    Abstract
    The asymmetric synthesis of ,-disubstituted -bisalkoxycarbonyl sulfonates is reported. The synthesis is based on the Michael addition of a lithiated enantiopure sulfonate bearing a cheap chiral sugar auxiliary to Knoevenagel acceptors. The reaction proceeds with high asymmetric inductions (ds=69-96%) and good yields (62-79%). The absolute configuration was determined by X-ray crystal-structure analysis  

    Diastereoselective construction of a functionalized dihydro-pyridazine-based spirooxindole scaffold: Via C-3 umpolung of isatin N, N ′-cyclic azomethine imine

    , Article New Journal of Chemistry ; Volume 43, Issue 26 , 2019 , Pages 10318-10323 ; 11440546 (ISSN) Matloubi Moghaddam, F ; Eslami, M ; Siahpoosh, A ; Hoda, G ; Sharif University of Technology
    Royal Society of Chemistry  2019
    Abstract
    Herein, functionalized spiro[indoline-3,5′-pyrazolo[1,2-a]pyridazine]-7′-carbonitrile containing two contiguous chiral stereocenters was efficiently synthesized in a satisfactory yield (up to 91% yield) and with excellent diastereoselectivity. We have reached this satisfactory yield by DABCO-catalyzed [3+3] annulation reactions of an isatin N,N′-cyclic azomethine imine 1,3-dipole with a Knoevenagel intermediate in dichloromethane (DCM) as solvent at ambient temperature; this was an entirely new strategy for creating one quaternary stereogenic center at the position-3 of an oxindole structure using an abnormal tandem Michael addition, N-cyclization, and a unique approach via the azomethine... 

    Diastereoselective construction of a functionalized dihydro-pyridazine-based spirooxindole scaffold: via C-3 umpolung of isatin N, N ′-cyclic azomethine imine

    , Article New Journal of Chemistry ; Volume 43, Issue 26 , 2019 , Pages 10318-10323 ; 11440546 (ISSN) Matloubi Moghaddam, F ; Eslami, M ; Siahpoosh, A ; Hoda, G ; Sharif University of Technology
    Royal Society of Chemistry  2019
    Abstract
    Herein, functionalized spiro[indoline-3,5′-pyrazolo[1,2-a]pyridazine]-7′-carbonitrile containing two contiguous chiral stereocenters was efficiently synthesized in a satisfactory yield (up to 91% yield) and with excellent diastereoselectivity. We have reached this satisfactory yield by DABCO-catalyzed [3+3] annulation reactions of an isatin N,N′-cyclic azomethine imine 1,3-dipole with a Knoevenagel intermediate in dichloromethane (DCM) as solvent at ambient temperature; this was an entirely new strategy for creating one quaternary stereogenic center at the position-3 of an oxindole structure using an abnormal tandem Michael addition, N-cyclization, and a unique approach via the azomethine... 

    A new domino Knoevenagel-hetero-Diels-Alder reaction: An efficient catalyst-free synthesis of novel thiochromone-annulated thiopyranocoumarin derivatives in aqueous medium

    , Article Tetrahedron ; Volume 66, Issue 45 , November , 2010 , Pages 8615-8622 ; 00404020 (ISSN) Matloubi Moghaddam, F ; Kiamehr, M ; Khodabakhshi, M. R ; Mirjafary, Z ; Fathi, S ; Saeidian, H ; Sharif University of Technology
    2010
    Abstract
    An efficient catalyst-free synthesis of novel pentacyclic thiochromone-annulated thiopyranocoumarin derivatives is achieved via domino Knoevenagel-hetero-Diels-Alder reaction of 4-hydroxy dithiocoumarin and O-acrylated salicylaldehyde derivatives in H2O as solvent. The products are formed in good yields with high regio- and stereo-selectivity