about
Synthesis, characterization and biological application of four novel metal-Schiff base complexes derived from allylamine and their interactions with human serum albumin: Experimental, molecular docking and ONIOM computational study.Sonocatalytic epoxidation of alkenes by vanadium-containing polyphosphomolybdate immobilized on multi-wall carbon nanotubes.Mild and efficient oxidation of alcohols with sodium periodate catalyzed by polystyrene-bound Mn(III)porphyrin.Efficient and selective hydrocarbon oxidation with sodium periodate under ultrasonic irradiation catalyzed by polystyrene-bound Mn (TPyP).Rapid and efficient oxidation of Hantzsch 1,4-dihydropyridines with sodium periodate catalyzed by manganese (III) Schiff base complexes.New porphyrin-polyoxometalate hybrid materials: synthesis, characterization and investigation of catalytic activity in acetylation reactions.A combined computational/experimental study on HSA binding of two water soluble Schiff base ligands derived from pyridine derivative and ethylendiamine.Novel Multicomponent Synthesis of Pyridine-Pyrimidines and Their Bis-Derivatives Catalyzed by Triazine Diphosphonium Hydrogen Sulfate Ionic Liquid Supported on Functionalized Nanosilica.Diastereoselective Synthesis of Symmetrical and Unsymmetrical Tetrahydropyridines Catalyzed by Bi(III) Immobilized on Triazine Dendrimer Stabilized Magnetic Nanoparticles.Elegant pH-Responsive Nanovehicle for Drug Delivery Based on Triazine Dendrimer Modified Magnetic Nanoparticles.New pyridinium-based ionic liquid as an excellent solvent-catalyst system for the one-pot three-component synthesis of 2,3-disubstituted quinolines.Self-recognition of the racemic ligand in the formation of homochiral dinuclear V(V) complex: In vitro anticancer activity, DNA and HSA interaction.Synthesis, characterization and separation of chiral and achiral diastereomers of Schiff base Pd(II) complex: A comparative study of their DNA- and HSA-binding.Performance Enhancement of Dye-Sensitized Solar Cells Based on TiO₂ Thick Mesoporous Photoanodes by Morphological Manipulation.Synthesis of Quinolines and Pyrido[3,2-g or 2,3-g]quinolines Catalyzed by Heterogeneous Propylphosphonium Tetrachloroindate Ionic LiquidCopper Immobilized on Nanosilica Triazine Dendrimer (Cu(II)-TD@nSiO2)-Catalyzed Regioselective Synthesis of 1,4-Disubstituted 1,2,3-Triazoles and Bis- and Tris-Triazoles via a One-Pot Multicomponent Click ReactionHydrocarbon oxidation catalyzed by vanadium polyoxometalate supported on mesoporous MCM-41 under ultrasonic irradiationSonocatalytic oxidation of olefins catalyzed by heteropolyanion-montmorillonite nanocompositePVC-Based Mn(III) Porphyrin Membrane-Coated Graphite Electrode for Determination of HistidineRegioselective multi-component synthesis of 1H-pyrazolo[3,4-d]pyrimidine-6(7H)-thionesA Novel pseudo-Four-Component Domino Reaction for the Synthesis of Naphtho[2,1-b]furan-2(1H)-ones Using a NanocatalystIn vitro antitumor activity of free and nano-encapsulated Na5[PMo10V2O40]·nH2O and its binding properties with ctDNA by using combined spectroscopic methodsIn vitro antitumor activity of parent and nano-encapsulated mono cobalt-substituted Keggin polyoxotungstate and its ctDNA binding propertiesIntroducing a dual-step procedure comprising microwave and electrical heating stages for the morphology-controlled synthesis of chromium-benzene dicarboxylate, MIL-101(Cr), applicable for CO2 adsorptionSynthesis of trans-1,3-diaryl-2-(5-methylisoxazol-3-yl)-2,3-dihydro-1H-naphtho[1,2-e][1,3]oxazines via bismuth(III)-catalyzed one-pot pseudo-four component reaction
P50
Q39567713-48697829-7E78-4BAE-847D-733B018EE009Q43251280-92D167DB-35F1-4381-9C95-2DE7ADA573C7Q46395327-D082A9F6-6750-47AB-938E-9F34191C6CD8Q46751692-986CEEFC-F76A-4444-903F-1E0118D7BA48Q46867733-9155D043-5317-4E13-98B1-FFF2F98F1EC8Q47247633-E26C7CE2-579D-450C-B73E-C5C11CB332BAQ47691383-E6D03849-49F6-4097-89A8-16EF92BDE916Q48159114-F732741C-C5CB-4CE4-9830-DBBA83065919Q48171279-4AF4AF12-688F-4739-B1E8-0C70BCC7D523Q48365049-B9D98899-4B69-415F-9B72-A3AAD2582FA4Q50461441-048100D0-0B67-4D75-8E0F-7CB4D21191A0Q51028027-7BFE85FF-09D4-464E-AA4F-FC67F9385619Q51532098-F3071C74-365F-4AA1-9D00-F834CC1ADD0DQ52913173-61C87FE1-5104-4341-B414-63DA5C865232Q58607700-AC75438F-8BEE-4C52-8090-FE1ABB946276Q71130472-CF70E50F-051F-4955-921E-CBFBE5C2B844Q80782993-30DFAFDB-EB2A-4489-984C-3B842DF1B41EQ84079529-D67467E4-8922-4732-91F2-79BBF493B7E1Q84331984-5F408A33-C1D9-429C-9A39-A198F36B7B8EQ84880958-76AE6FCE-D151-4C2A-946A-3685D5DEF4AAQ85533625-52C643D2-E7E9-4DF1-ADD9-3325B3CBE963Q86113439-8F2E18E4-730E-4D4C-B0FE-EFDCC7E36381Q87419291-4DB77B3B-3E49-4300-B713-ED8AF89DC3E4Q93013978-BF7C87D0-392D-403C-A4DC-9A482AD7616FQ95445951-FDF575E9-ABD2-4880-A3B9-E70A0A0003AE
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Shahram Tangestaninejad
@en
Shahram Tangestaninejad
@nl
type
label
Shahram Tangestaninejad
@en
Shahram Tangestaninejad
@nl
prefLabel
Shahram Tangestaninejad
@en
Shahram Tangestaninejad
@nl
P31
P496
0000-0001-5263-9795