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Mostafa Kiamehr

Researcher at University of Qom

Publications -  32
Citations -  325

Mostafa Kiamehr is an academic researcher from University of Qom. The author has contributed to research in topics: Diels–Alder reaction & Knoevenagel condensation. The author has an hindex of 9, co-authored 32 publications receiving 284 citations. Previous affiliations of Mostafa Kiamehr include University of Rostock & Sharif University of Technology.

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

TL;DR: In this article, 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 CH 3 CN in the presence of 10 ǫ% of ZnO as a heterogeneous catalyst.
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Facile entry to polycyclic indolylhydroquinoline skeletons via tandem C-alkylation and intramolecular S-alkylation

TL;DR: In this paper, a single step synthesis of indole-annulated pentacyclic indolylhydroquinolines via tandem C-alkylation and intramolecular S-kylation of indolin-2-thiones with Nalkylquinolinium salts in excellent yields was reported.
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Synthesis of Novel Polycyclic Indole‐Annulated Thiopyranocoumarin Derivatives via Domino Knoevenagel–Hetero‐Diels–Alder Reaction in Aqueous Media

TL;DR: In this paper, an efficient polycyclic indole derivatives were obtained via the domino Knoevenagel-hetero-Diels-Alder reaction of O-acrylated salicylaldehyde derivatives with dihydroindole-2-thiones in H2O as solvent.
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A new domino Knoevenagel-hetero-Diels–Alder reaction: an efficient catalyst-free synthesis of novel thiochromone-annulated thiopyranocoumarin derivatives in aqueous medium

TL;DR: An efficient catalyst-free synthesis of novel pentacyclic thiochromone-annulated thiopyranocoumarin derivatives was achieved via domino Knoevenagel-hetero-Diels-Alder reaction.
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Pyridinium salts—versatile reagents for the regioselective synthesis of functionalized thiazocino[2,3-b]indoles by tandem dinucleophilic reactions of thiooxindoles

TL;DR: The reaction of thiooxindoles with various 2- and 3-substituted pyridinium salts afforded a variety of functionalized thiazocinoindoles that have been prepared in good to excellent yields by regioselective dinucleophilic C/S-cyclocondensation.