M
Mehdi Bakavoli
Researcher at Ferdowsi University of Mashhad
Publications - 329
Citations - 3436
Mehdi Bakavoli is an academic researcher from Ferdowsi University of Mashhad. The author has contributed to research in topics: Catalysis & Aryl. The author has an hindex of 26, co-authored 329 publications receiving 3067 citations. Previous affiliations of Mehdi Bakavoli include University of Wollongong & Payame Noor University.
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Journal ArticleDOI
Molecular iodine promoted synthesis of new pyrazolo[3,4-d]pyrimidine derivatives as potential antibacterial agents.
Mehdi Bakavoli,Ghodsieh Bagherzadeh,Maryam Vaseghifar,Ali Shiri,Mehdi Pordel,Mansour Mashreghi,Parvaneh Pordeli,Maryam Araghi +7 more
TL;DR: Iodocyclization of 5-amino-1-dinitrophenyl)-1H-4-pyrazolcarboxamides with aromatic aldehydes gave a new series of pyrazolo[3,4-d]pyrimidine derivatives in a single step and their antibacterial activity comparable to Streptomycin as reference drug was evaluated.
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Design and synthesis of pyrimido[4,5-b][1,4]benzothiazine derivatives, as potent 15-lipoxygenase inhibitors.
TL;DR: A group of 2-substituted pyrimido[4,5-b][1,4]benzothiazines designed, synthesized, and evaluated as potential inhibitors of 15-lipoxygenase suggest the interaction of the iron atom is essential for the activity of the inhibitors.
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Highly efficient, one-pot, solvent-free synthesis of 2,4,6-triarylpyridines using a Brønsted-acidic ionic liquid as reusable catalyst
TL;DR: In this article, a simple, efficient, and green method for synthesis of 2,4,6-triarylpyridines by one-pot three-component reaction of acetophenones, aryl aldehydes, and ammonium acetate using 3-methyl-1-(4-sulfonylbutyl)imidazolium hydrogen sulfate [HO3S(CH2)4MIM][HSO4], a Bronsted-acidic ionic liquid, as an effective and reusable catalyst under solvent-free conditions is described.
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Pd–Cu catalyzed heterocyclization during Sonogashira coupling: synthesis of 3-benzylthiazolo[3,2-a]benzimidazole
TL;DR: The reaction of 2-mercaptopropargyl benzimidazole with various iodobenzenes catalyzed by Pd-Cu leads to the formation of 3-benzylthiazolo[3,2-a]benzimidazesoles.
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Regioselective synthesis of 6-benzylthiazolo-[3,2-b]1,2,4-triazoles during Sonogashira coupling
Majid M. Heravi,Ali Kivanloo,Mohammad Rahimzadeh,Mehdi Bakavoli,Mitra Ghassemzadeh,Bernhard Neumüller +5 more
TL;DR: The reaction of 3-mercaptopropargyl-1,2,4-triazoles with various iodobenzenes catalyzed by Pd-Cu leads to the regioselective formation of 6-benzylthiazolo as discussed by the authors.