Behzad Zeynizadeh
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Interests
Behzad Zeynizadeh has a total of 66 co-authors. Here are the top co-authors by number of shared publications:
- Hossein Mousavi
Department of Organic Chemistry, Faculty of Chemistry, Urmia University, Urmia, Iran
8 shared publications - Esmail Doustkhah
Chemistry Department, Faculty of Engineering and Natural Sciences, Istinye University, Sariyer, Istanbul 34396, Türkiye
5 shared publications - Mehri Kouhkan
Urmia Univ, Fac Sci, Dept Chem, Orumiyeh, Iran
5 shared publications - Sadegh Rostamnia
Organic and Nano Group (ONG), Department of Chemistry, Iran University of Science and Technology (IUST), PO Box 16846-13114, Tehran, Iran
5 shared publications - Soleiman Rahmani
Faculty of Chemistry, Urmia University, Urmia 5756151818, Iran
5 shared publications Morteza Hasanpour Galehban
Department of Organic Chemistry, Faculty of Chemistry, Urmia University, Urmia, Iran
4 shared publications
Latest Publications
- Open Access
- 9 May 2025
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 7 (12) , 3701-3721
Magnetically recoverable Fe 3 O 4 @chitosan@Ni 2 B: a bio-based catalyst for one-pot green and efficient synthesis of tetrahydrobenzo[ b ]pyrans
This study investigates the development of a novel and environmentally friendly catalyst, Fe 3 O 4 @chitosan@Ni 2 B nanocomposite, for synthesis of tetrahydrobenzo[ b ]pyrans.
- 9 May 2025
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 7 (12) , 3701-3721
Open AccessMagnetically recoverable Fe 3 O 4 @chitosan@Ni 2 B: a bio-based catalyst for one-pot green and efficient synthesis of tetrahydrobenzo[ b ]pyrans
This study investigates the development of a novel and environmentally friendly catalyst, Fe 3 O 4 @chitosan@Ni 2 B nanocomposite, for synthesis of tetrahydrobenzo[ b ]pyrans.
- Open Access
- 10 March 2025
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 7 (9) , 2528-2553
Green procedures for synthesizing potential h NMDA receptor allosteric modulators through reduction and one-pot reductive acetylation of nitro(hetero)arenes using a superparamagnetic Fe 3 O 4 @APTMS@Cp 2 ZrCl x ( x = 0, 1, 2) nanocatalyst
In this research, we have developed diverse strategies for synthesizing potential h NMDA receptor allosteric modulators through reduction and one-pot reductive acetylation of nitro(hetero)arenes using a mesoporous zirconocene-containing nanocatalyst.
- 10 March 2025
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 7 (9) , 2528-2553
Open AccessGreen procedures for synthesizing potential h NMDA receptor allosteric modulators through reduction and one-pot reductive acetylation of nitro(hetero)arenes using a superparamagnetic Fe 3 O 4 @APTMS@Cp 2 ZrCl x ( x = 0, 1, 2) nanocatalyst
In this research, we have developed diverse strategies for synthesizing potential h NMDA receptor allosteric modulators through reduction and one-pot reductive acetylation of nitro(hetero)arenes using a mesoporous zirconocene-containing nanocatalyst.
- Open Access
- 1 January 2025
- Published by Green Publication
- Vol. 28 (2S) , 117-123
Synthesis And Characterization Of Nanocomposite Hydrogel Scaffolds Based On Chitosan/Sodium Alginate Containing Halloysite Nanotubes With Biomedical Applications
This study aimed to develop hybrid hydrogel beads as biocompatible scaffolds using chitosan (CS) and sodium alginate (Alg), incorporating varying concentrations of halloysite nanotubes (Hal) (3, 6, and 9% w/w) and cross-linked with Ca²+ ions. The synthesized hydrogels were thoroughly characterized using various analytical techniques, including FTIR, XRD, SEM/EDX, and TEM. The varying Hal concentrations significantly influenced the properties of the hydrogels, as evidenced by swelling behavior analysis, which revealed a decrease in swelling capacity with an increase in Hal content. The water uptake capacity was decreased along with an increase in the percentage of Hal in hydrogels. All hydrogels revealed a substantial water content exceeding 80%. The addition of Hal had a non-significant effect on the water retention abilities of the hydrogels. The hemolysis test showed good hemostatic properties of the hydrogels. Therefore, hydrogels showed hopeful application properties in biomedical applications.
- 1 January 2025
- Published by Green Publication
- Vol. 28 (2S) , 117-123
Open AccessSynthesis And Characterization Of Nanocomposite Hydrogel Scaffolds Based On Chitosan/Sodium Alginate Containing Halloysite Nanotubes With Biomedical Applications
This study aimed to develop hybrid hydrogel beads as biocompatible scaffolds using chitosan (CS) and sodium alginate (Alg), incorporating varying concentrations of halloysite nanotubes (Hal) (3, 6, and 9% w/w) and cross-linked with Ca²+ ions. The synthesized hydrogels were thoroughly characterized using various analytical techniques, including FTIR, XRD, SEM/EDX, and TEM. The varying Hal concentrations significantly influenced the properties of the hydrogels, as evidenced by swelling behavior analysis, which revealed a decrease in swelling capacity with an increase in Hal content. The water uptake capacity was decreased along with an increase in the percentage of Hal in hydrogels. All hydrogels revealed a substantial water content exceeding 80%. The addition of Hal had a non-significant effect on the water retention abilities of the hydrogels. The hemolysis test showed good hemostatic properties of the hydrogels. Therefore, hydrogels showed hopeful application properties in biomedical applications.
- Open Access
- 25 June 2024
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 6 (15) , 3961-3977
NiII-containing l-glutamic acid cross-linked chitosan anchored on Fe3O4/f-MWCNT: a sustainable catalyst for the green reduction and one-pot two-step reductive Schotten–Baumann-type acetylation of nitroarenes
In this research, new catalytic applications of the Fe3O4/f-MWCNT-CS-Glu/NiII nanocomposite have been introduced for the efficient reduction and one-pot two-step reductive Schotten–Baumann-type acetylation of nitroarenes in water.
- 25 June 2024
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 6 (15) , 3961-3977
Open AccessNiII-containing l-glutamic acid cross-linked chitosan anchored on Fe3O4/f-MWCNT: a sustainable catalyst for the green reduction and one-pot two-step reductive Schotten–Baumann-type acetylation of nitroarenes
In this research, new catalytic applications of the Fe3O4/f-MWCNT-CS-Glu/NiII nanocomposite have been introduced for the efficient reduction and one-pot two-step reductive Schotten–Baumann-type acetylation of nitroarenes in water.
- 22 April 2024
- Published by American Chemical Society (ACS) in ACS Chemical Neuroscience
- Vol. 15 (9) , 1828-1881
Practical Three-Component Regioselective Synthesis of Drug-Like 3-Aryl(or heteroaryl)-5,6-dihydrobenzo[h]cinnolines as Potential Non-Covalent Multi-Targeting Inhibitors To Combat Neurodegenerative Diseases
Neurodegenerative diseases (NDs) are one of the prominent health challenges facing contemporary society, and many efforts have been made to overcome and (or) control it. In this research paper, we described a practical one-pot two-step three-component reaction between 3,4-dihydronaphthalen-1(2H)-one (1), aryl(or heteroaryl)glyoxal monohydrates (2a-h), and hydrazine monohydrate (NH2NH2•H2O) for the regioselective preparation of some 3-aryl(or heteroaryl)-5,6-dihydrobenzo[h]cinnoline derivatives (3a-h). After synthesis and characterization of the mentioned cinnolines (3a-h), the in silico multi-targeting inhibitory properties of these heterocyclic scaffolds have been investigated upon various Homo sapiens-type enzymes, including hMAO-A, hMAO-B, hAChE, hBChE, hBACE-1, hBACE-2, hNQO-1, hNQO-2, hnNOS, hiNOS, hPARP-1, hPARP-2, hLRRK-2(G2019S), hGSK-3β, hp38α MAPK, hJNK-3, hOGA, hNMDA receptor, hnSMase-2, hIDO-1, hCOMT, hLIMK-1, hLIMK-2, hRIPK-1, hUCH-L1, hPARK-7, and hDHODH, which have confirmed their functions and roles in the neurodegenerative diseases (NDs), based on molecular docking studies, and the obtained results were compared with a wide range of approved drugs and well-known (with IC50, EC50, etc.) compounds. In addition, in silico ADMET prediction analysis was performed to examine the prospective drug properties of the synthesized heterocyclic compounds (3a-h). The obtained results from the molecular docking studies and ADMET-related data demonstrated that these series of 3-aryl(or heteroaryl)-5,6-dihydrobenzo[h]cinnolines (3a-h), especially hit ones, can really be turned into the potent core of new drugs for the treatment of neurodegenerative diseases (NDs), and/or due to the having some reactionable locations, they are able to have further organic reactions (such as cross-coupling reactions), and expansion of these compounds (for example, with using other types of aryl(or heteroaryl)glyoxal monohydrates) makes a new avenue for designing novel and efficient drugs for this purpose.
- 22 April 2024
- Published by American Chemical Society (ACS) in ACS Chemical Neuroscience
- Vol. 15 (9) , 1828-1881
Practical Three-Component Regioselective Synthesis of Drug-Like 3-Aryl(or heteroaryl)-5,6-dihydrobenzo[h]cinnolines as Potential Non-Covalent Multi-Targeting Inhibitors To Combat Neurodegenerative Diseases
Neurodegenerative diseases (NDs) are one of the prominent health challenges facing contemporary society, and many efforts have been made to overcome and (or) control it. In this research paper, we described a practical one-pot two-step three-component reaction between 3,4-dihydronaphthalen-1(2H)-one (1), aryl(or heteroaryl)glyoxal monohydrates (2a-h), and hydrazine monohydrate (NH2NH2•H2O) for the regioselective preparation of some 3-aryl(or heteroaryl)-5,6-dihydrobenzo[h]cinnoline derivatives (3a-h). After synthesis and characterization of the mentioned cinnolines (3a-h), the in silico multi-targeting inhibitory properties of these heterocyclic scaffolds have been investigated upon various Homo sapiens-type enzymes, including hMAO-A, hMAO-B, hAChE, hBChE, hBACE-1, hBACE-2, hNQO-1, hNQO-2, hnNOS, hiNOS, hPARP-1, hPARP-2, hLRRK-2(G2019S), hGSK-3β, hp38α MAPK, hJNK-3, hOGA, hNMDA receptor, hnSMase-2, hIDO-1, hCOMT, hLIMK-1, hLIMK-2, hRIPK-1, hUCH-L1, hPARK-7, and hDHODH, which have confirmed their functions and roles in the neurodegenerative diseases (NDs), based on molecular docking studies, and the obtained results were compared with a wide range of approved drugs and well-known (with IC50, EC50, etc.) compounds. In addition, in silico ADMET prediction analysis was performed to examine the prospective drug properties of the synthesized heterocyclic compounds (3a-h). The obtained results from the molecular docking studies and ADMET-related data demonstrated that these series of 3-aryl(or heteroaryl)-5,6-dihydrobenzo[h]cinnolines (3a-h), especially hit ones, can really be turned into the potent core of new drugs for the treatment of neurodegenerative diseases (NDs), and/or due to the having some reactionable locations, they are able to have further organic reactions (such as cross-coupling reactions), and expansion of these compounds (for example, with using other types of aryl(or heteroaryl)glyoxal monohydrates) makes a new avenue for designing novel and efficient drugs for this purpose.
- Open Access
- 9 August 2023
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 5 (17) , 4499-4520
Immobilized nickel boride nanoparticles on magnetic functionalized multi-walled carbon nanotubes: a new nanocomposite for the efficient one-pot synthesis of 1,4-benzodiazepines
In this study, a new nanocomposite consisting of Ni2B nanoparticles anchored on magnetic functionalized multi-walled carbon nanotubes (Fe3O4/f-MWCNT/Ni2B) was synthesized and successfully used for the preparation of bioactive 1,4-benzodiazepines.
- 9 August 2023
- Published by Royal Society of Chemistry (RSC) in Nanoscale Advances
- Vol. 5 (17) , 4499-4520
Open AccessImmobilized nickel boride nanoparticles on magnetic functionalized multi-walled carbon nanotubes: a new nanocomposite for the efficient one-pot synthesis of 1,4-benzodiazepines
In this study, a new nanocomposite consisting of Ni2B nanoparticles anchored on magnetic functionalized multi-walled carbon nanotubes (Fe3O4/f-MWCNT/Ni2B) was synthesized and successfully used for the preparation of bioactive 1,4-benzodiazepines.
- Open Access
- 1 June 2022
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 12 (26) , 16454-16478
Ni II NPs entrapped within a matrix of l -glutamic acid cross-linked chitosan supported on magnetic carboxylic acid-functionalized multi-walled carbon nanotube: a new and efficient multi-task catalytic system for the green one-pot synthesis of diverse heterocyclic frameworks
In this research work, an Fe 3 O 4 / f -MWCNT-CS-Glu/Ni II hybrid nanocomposite was synthesized, characterized, and used as a new and efficient multi-task catalytic system for the green one-pot synthesis of diverse heterocyclic frameworks.
- 1 June 2022
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 12 (26) , 16454-16478
Open AccessNi II NPs entrapped within a matrix of l -glutamic acid cross-linked chitosan supported on magnetic carboxylic acid-functionalized multi-walled carbon nanotube: a new and efficient multi-task catalytic system for the green one-pot synthesis of diverse heterocyclic frameworks
In this research work, an Fe 3 O 4 / f -MWCNT-CS-Glu/Ni II hybrid nanocomposite was synthesized, characterized, and used as a new and efficient multi-task catalytic system for the green one-pot synthesis of diverse heterocyclic frameworks.
- Open Access
- 17 May 2022
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 12 (24) , 15020-15037
A uniformly anchored zirconocene complex on magnetic reduced graphene oxide (rGO@Fe 3 O 4 /ZrCp 2 Cl x ( x = 0, 1, 2) ) as a novel and reusable nanocatalyst for synthesis of N -arylacetamides and reductive-acetylation of nitroarenes
In this study, a crafted zirconocene complex on rGO@Fe 3 O 4 as a novel magnetic nanocatalyst was synthesized and then characterized using FT-IR, SEM, EDX, VSM, ICP-OES, TGA, BET and MS analyses.
- 17 May 2022
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 12 (24) , 15020-15037
Open AccessA uniformly anchored zirconocene complex on magnetic reduced graphene oxide (rGO@Fe 3 O 4 /ZrCp 2 Cl x ( x = 0, 1, 2) ) as a novel and reusable nanocatalyst for synthesis of N -arylacetamides and reductive-acetylation of nitroarenes
In this study, a crafted zirconocene complex on rGO@Fe 3 O 4 as a novel magnetic nanocatalyst was synthesized and then characterized using FT-IR, SEM, EDX, VSM, ICP-OES, TGA, BET and MS analyses.
- Open Access
- 7 April 2022
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 12 (18) , 11164-11189
Diverse and efficient catalytic applications of new cockscomb flower-like Fe3O4@SiO2@KCC-1@MPTMS@CuIImesoporous nanocomposite in the environmentally benign reduction and reductive acetylation of nitroarenes and one-pot synthesis of some coumarin compounds
Herein, a new cockscomb flower-like Fe3O4@SiO2@KCC-1@MPTMS@CuIImesoporous nanocomposite was synthesized, characterized, and used in the green reduction and reductive acetylation of nitroarenes and one-pot synthesis of some coumarin compounds.
- 7 April 2022
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 12 (18) , 11164-11189
Open AccessDiverse and efficient catalytic applications of new cockscomb flower-like Fe3O4@SiO2@KCC-1@MPTMS@CuIImesoporous nanocomposite in the environmentally benign reduction and reductive acetylation of nitroarenes and one-pot synthesis of some coumarin compounds
Herein, a new cockscomb flower-like Fe3O4@SiO2@KCC-1@MPTMS@CuIImesoporous nanocomposite was synthesized, characterized, and used in the green reduction and reductive acetylation of nitroarenes and one-pot synthesis of some coumarin compounds.