Name Hassan Sepehrmansourie Affiliation دانشجوی دانشگاه بوعلی سینا Degree _ Website Email — JournalPaper Presentation Speech WorkShop Book Innovation GrantAttraction Thesis Festival FinishedProject Sales Art Membership StandardCreation Publication TheorizingChair TitleJournal 1 Laser-assisted Synthesis of Pd/Metal-Organic Framework and Its Application in the Sensing of Ethanol and Methanol Vapors International journal of optics and photonics 2 Synthesis of picolinates via a cooperative vinylogous anomeric-based oxidation using UiO66(Zr)-N(CH2PO3H2)2 as a catalyst† RSC Advances 3 A New Approach for the Synthesis of Bis(3- Indolyl)Pyridines via a Cooperative Vinylogous Anomeric Based Oxidation Using Ammonium Acetate as a Dual Reagent-Catalyst Role under Mild and Green Condition POLYCYCLIC AROMATIC COMPOUNDS 4 Application of Metal−Organic Frameworks with Sulfonic Acid Tags in the Synthesis of Pyrazolo[3,4‑b]pyridines via a Cooperative Vinylogous Anomeric-Based Oxidation INORGANIC CHEMISTRY 5 A MOF-on-MOF strategy to construct double Z-scheme heterojunction for high-performance photocatalytic degradation APPLIED CATALYSIS B-ENVIRONMENTAL 6 Nanoarchitecting a Dual Z-Scheme Zr-MOF/Ti-MOF/g-C3N4 Heterojunction for Boosting Gomberg–Buchmann–Hey Reactions under Visible Light Conditions ACS Sustainable Chemistry & Engineering 7 Catalytic Application of Functionalized Bimetallic−Organic Frameworks with Phosphorous Acid Tags in the Synthesis of Pyrazolo[4,3‑e]pyridines ACS Omega 8 Application of Nanomagnetic Metal−Organic Frameworks in the Green Synthesis of Nicotinonitriles via Cooperative Vinylogous Anomeric-Based Oxidation ACS Omega 9 Application of Zr‑MOFs based copper complex in synthesis of pyrazolo[3, 4‑b]pyridine‑5‑carbonitriles via anomeric‑based oxidation Scientific Reports 10 Convergent paired electrosynthesis of different types of bis-β-diketone derivatives based on the knoevenagel condensation reaction under green conditions ELECTROCHIMICA ACTA 11 Applications of novel composite UiO-66-NH2/ Melamine with phosphorous acid tags as a porous and efficient catalyst for the preparation of novel spiro-oxindoles NEW JOURNAL OF CHEMISTRY 12 Catalytic chemo and homoselective ipso-nitration under mild condition Molecular Catalysis 13 Catalytic synthesis of new pyrazolo [3,4‑b] pyridine via a coopera tive vinylogous anomeric‑based oxidation Scientific Reports 14 Phosphonic acid tagged carbon quantum dots encapsulated in SBA‑15 as a novel catalyst for the preparation of N‑heterocycles with pyrazolo, barbituric acid and indole moieties Scientific Reports 15 A convenient catalytic method for preparation of new tetrahydropyrido[2,3-d]pyrimidines via a cooperative vinylogous anomeric based oxidation RSC Advances 16 Synthesis and Application of Novel Magnetic Glycoluril Tetrakis(Methylene Phosphorous Acid) as a Nano Biological Catalyst for the Preparation of Nicotinonitriles via a Cooperative Vinylogous Anomeric-Based Oxidation POLYCYCLIC AROMATIC COMPOUNDS 17 Application of novel nanomagnetic metal–organic frameworks as a catalyst for the synthesis of new pyridines and 1,4‑dihydropyridines via a cooperative vinylogous anomeric based oxidation Scientific Reports 18 Novel uric acid-based nano organocatalyst with phosphorous acid tags: Application for synthesis of new biologically-interest pyridines with indole moieties via a cooperative vinylogous anomeric based oxidation Molecular Catalysis 19 Anodic electrosynthesis of MIL‑53(Al)‑N(CH2PO3H2)2 as a mesoporous catalyst for synthesis of novel (N‑methyl‑pyrrol)‑pyrazolo[3,4‑b] pyridines via a cooperative vinylogous anomeric based oxidation Scientific Reports 20 Multilinker phosphorous acid anchored En/MIL-100(Cr) as a novel nanoporous catalyst for the synthesis of new N-heterocyclic pyrimido[4,5-b] quinolines Molecular Catalysis 21 Mesoporous Ionically Tagged Cross-Linked Poly(vinyl imidazole)s as Novel and Reusable Catalysts for the Preparation of N‑Heterocycle Spiropyrans ACS Omega 22 Novel nano-size and crab-like biological-based glycoluril with sulfonic acid tags as a reusable catalyst: its application to the synthesis of new mono- and bis-spiropyrans and their in vitro biological studies NEW JOURNAL OF CHEMISTRY