دسترسی یکپارچه به مقالات، کتابها و ارائههای علمی استاد دکتر محمدعلی زلفیگل؛ گردآوریشده از منابع معتبر دانشگاهی
RSC Advances Vol. 3, No. 48, 25681–25681
In this study, a green, simple and efficient method for the preparation of 6-amino-4-(4-methoxyphenyl)-5-cyano-3-methyl-1-phenyl-1,4-dihydropyrano[2,3-c]pyrazoles by means of a one-pot four component condensation reaction of aryl aldehydes,…
DOI: 10.1039/c3ra45289aNew Journal of Chemistry Vol. 37, No. 12, 4089–4089
In this work, disulfonic acid imidazolium chloroaluminate {[Dsim]AlCl4} is applied as a new acidic and heterogeneous catalyst for green, simple and efficient synthesis of 6-amino-4-(4-methoxyphenyl)-5-cyano-3-methyl-1-phenyl-1,4-dihydropyra…
DOI: 10.1039/c3nj00629hRSC Advances Vol. 3, No. 21, 7692–7692
WCl6 was used as a novel, efficient and reusable catalyst for the preparation of N-sulfonyl imines via the condensation of sulfonamides with aldehydes as well as isatin under solvent-free conditions. The turn-over frequency (TOF) value of t…
DOI: 10.1039/c3ra40681dJournal of Chemistry Vol. 2013, No. 1
A good range of 1,4‐dihydropyridines bearing a carbamate moiety on the 4‐position were synthesized from the primary reaction of different hydroxyaldehydes with phenyl isocyanates and the subsequent reaction of the obtained carbamates with m…
DOI: 10.1155/2013/495982Journal of the Iranian Chemical Society Vol. 10, No. 3, 577–581
DOI: 10.1007/s13738-012-0193-1Journal of Molecular Liquids Vol. 178, 113–121
DOI: 10.1016/j.molliq.2012.10.045Journal of Reports in Pharmaceutical Sciences Vol. 1, No. 2, 87–93
Abstract: In a wide search program towards new and efficient antimicrobial agents, a series of 4-substituted-1,2,4-triazolidine-3,5-dione derivatives namely urazoles holding an alkyl moiety at position 4 have been synthesized and tested for…
DOI: 10.22110/jrps.v1i2.701ChemInform Vol. 43, No. 49
Abstract A multi‐step one‐pot procedure for the synthesis of the title compounds is reported in relative short reaction times.
DOI: 10.1002/chin.201249158ChemInform Vol. 43, No. 49
Abstract Sulfonic acid coated γ‐Fe2O3 nanoparticles catalyze the Hantzsch synthesis of dihydropyridines under solvent‐free conditions.
DOI: 10.1002/chin.201249155Chinese Chemical Letters Vol. 23, No. 12, 1323–1326
DOI: 10.1016/j.cclet.2012.10.006ChemInform Vol. 43, No. 48
DOI: 10.1002/chin.201248029Journal of Heterocyclic Chemistry Vol. 49, No. 6, 1429–1433
Syntheses of polyindolyl compounds from the Friedel–Crafts reaction of indoles and tri‐ or tetra‐aldehydes catalyzed by silica sulfuric acid are described. These dendrimeric supramolecules were effectively prepared at room temperature in qu…
DOI: 10.1002/jhet.929Journal of Industrial and Engineering Chemistry Vol. 19, No. 3, 721–726
DOI: 10.1016/j.jiec.2012.10.014Tetrahedron Vol. 69, No. 1, 212–218
DOI: 10.1016/j.tet.2012.10.042ChemInform Vol. 43, No. 43
Abstract A simple protocol allows for the synthesis of the title compounds (V) by Ugi‐four component reaction of arylidenepyruvic acids, amines, aldehydes, and isocyanides.
DOI: 10.1002/chin.201243069Synthetic Communications Vol. 43, No. 1, 52–58
The oxidative conversion of alcohols or aldehydes to the corresponding nitriles in moderate to good yields was easily achieved by treatment of H5IO6 and KI in aqueous NH3. This simple and one-pot system provides easy workup and separation o…
DOI: 10.1080/00397911.2011.591035Letters in Organic Chemistry Vol. 9, No. 8, 598–603
Silica bromide as heterogeneous reagent is prepared from the reaction of silica gel with PBr3 as a nonhydroscopic, filterable, cheap, and stable yellowish powder that can be stored for months. The results show that the silica bromide is a s…
DOI: 10.2174/157017812802850285Bulletin of the Korean Chemical Society Vol. 33, No. 8, 2619–2622
Bromination and iodination of the aromatic compounds have efficiently been carried out at room temperature and $70^{\circ}C$ , respectively, in short reaction times using orthoperiodic acid/sodium bromide (1:2) and orthoperiodic acid/sodium…
DOI: 10.5012/bkcs.2012.33.8.2619American Journal of Organic Chemistry Vol. 2, No. 4, 97–104
Abstarct A simple, highly efficient and green procedure for the condensation of aryl and alkyl 1,2-diamines with α-diketones in the presence of catalytic amount of phenol(20 mol%) at room temperature is described. Using this method, quinoxa…
DOI: 10.5923/j.ajoc.20120204.04Scientia Iranica Vol. 19, No. 6, 1584–1590
A simple and highly efficient method for the protection of amines from their corresponding N-boc derivatives is reported. It is interesting that only 0.1 mol % of novel ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate {[Dsim] H…
DOI: 10.1016/j.scient.2012.05.003ChemInform Vol. 43, No. 35
ChemInformVolume 43, Issue 35 Isocyclic Compounds ChemInform Abstract: Solid-Supported Sulfonic Acid-Containing Catalysts Efficiently Promoted One-Pot Multicomponent Synthesis of β-Acetamido Carbonyl Compounds. Mohammad Ali Zolfigol, Mohamm…
DOI: 10.1002/chin.201235062ChemInform Vol. 43, No. 35
Abstract The present protocol is characterized by clean reactions, simple purification, short reaction times and, as compared to established methods, higher turn over frequencies.
DOI: 10.1002/chin.201235029ChemInform Vol. 43, No. 33
Abstract Tribromoisocyanuric acid in the presence of wet SiO2 is a suitable reagent for the regeneration of carbonyl compounds from oximes, semicarbazones, azines, and Schiff bases under mild conditions.
DOI: 10.1002/chin.201233050ChemInform Vol. 43, No. 32
Abstract The new ionic liquid allows efficient nitration of various aromatic compounds.
DOI: 10.1002/chin.201232056