Hamid Aliyan
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Hamid Aliyan has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
- Razieh Fazaeli
Islamic Azad University
3 shared publications Hamid Javaherian Naghash
Department of Chemistry, Islamic Azad University, Shahreza Branch, Shahreza 86145‐311, Iran
2 shared publicationsAhmad Reza Massah
Department of Chemistry, Islamic Azad University, Shahreza Branch, Shahreza 86145‐311, Iran
1 shared publication- Ahmad Reza Momeni
The University of Shahrekord
1 shared publication Ahmad Reza Mssah
Department of Chemistry, Islamic Azad University, Shahreza Branch, 86145-311, Iran
1 shared publicationGinous Emami
Department of Chemistry, Islamic Azad University, Shahreza Branch, 86145-311, Iran
1 shared publication
Latest Publications
- 1 August 2020
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 98 (8) , 445-452
Pd/APN-Mn(BTC) as novel, highly efficient, and recyclable catalyst for Suzuki–Miyaura cross coupling reaction
A novel, heterogeneous, and bifunctional metal organic framework containing palladium and manganese, Pd/APN-Mn(BTC), has been prepared and completely characterized using FTIR, XRD, SEM-EDS, N2 adsorption–desorption, TG-DTG, NH3-TPD, and ICP analytical techniques. The APN-Mn(BTC) framework has been shown to be a useful platform for the stabilization and support of palladium nanoparticles (Pd NPs). Very effective catalytic activity has been exhibited by the highly dispersed Pd particles, Pd-NPs/APN-Mn(BTC), in the Suzuki–Miyaura cross-coupling reaction with reasonable to excellent reaction yields under mild conditions in H2O–ethanol solvent.
- 1 August 2020
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 98 (8) , 445-452
Pd/APN-Mn(BTC) as novel, highly efficient, and recyclable catalyst for Suzuki–Miyaura cross coupling reaction
A novel, heterogeneous, and bifunctional metal organic framework containing palladium and manganese, Pd/APN-Mn(BTC), has been prepared and completely characterized using FTIR, XRD, SEM-EDS, N2 adsorption–desorption, TG-DTG, NH3-TPD, and ICP analytical techniques. The APN-Mn(BTC) framework has been shown to be a useful platform for the stabilization and support of palladium nanoparticles (Pd NPs). Very effective catalytic activity has been exhibited by the highly dispersed Pd particles, Pd-NPs/APN-Mn(BTC), in the Suzuki–Miyaura cross-coupling reaction with reasonable to excellent reaction yields under mild conditions in H2O–ethanol solvent.
- 1 October 2018
- Vol. 6 (4, pp. 325) , 230-238
Friedel-Crafts alkylation of indoles with epoxides using PW12-APTES@SBA-15
- 1 October 2018
- Vol. 6 (4, pp. 325) , 230-238
Friedel-Crafts alkylation of indoles with epoxides using PW12-APTES@SBA-15
- 1 January 2009
- Published by Wiley in Heteroatom Chemistry
- Vol. 20 (6) , 325-331
Bulk and supported tungstophosphoric acid as friendly, efficient, recyclable catalysts for the synthesis of bis-indolylmethanes under solvent-free conditions
- 1 January 2009
- Published by Wiley in Heteroatom Chemistry
- Vol. 20 (6) , 325-331
Bulk and supported tungstophosphoric acid as friendly, efficient, recyclable catalysts for the synthesis of bis-indolylmethanes under solvent-free conditions
- 1 January 2009
- Published by Wiley in Heteroatom Chemistry
- Vol. 20 (4) , 202-207
Facile route for the synthesis of benzothiazoles and benzimidazoles in the presence of tungstophosphoric acid impregnated zirconium phosphate under solvent‐free conditions
Rapid and efficient condensation reactions of o‐phenylenediamine and o‐aminothiophenol with various aldehydes were carried out using tungstophosphoric acid impregnated zirconium phosphate in solvent‐free conditions to afford the corresponding 2‐substituted arylbenzimidazole and arylbenzothiazole derivatives in good to excellent yields. This procedure constitutes a simple and practical green synthetic method for 2‐arylbenzimidazoles and 2‐arylbenzothiazoles and their structural analogs. Furthermore, the catalyst can be reused for several times but it will be less active. © 2009 Wiley Periodicals, Inc. Heteroatom Chem 20:202–207, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20534
- 1 January 2009
- Published by Wiley in Heteroatom Chemistry
- Vol. 20 (4) , 202-207
Facile route for the synthesis of benzothiazoles and benzimidazoles in the presence of tungstophosphoric acid impregnated zirconium phosphate under solvent‐free conditions
Rapid and efficient condensation reactions of o‐phenylenediamine and o‐aminothiophenol with various aldehydes were carried out using tungstophosphoric acid impregnated zirconium phosphate in solvent‐free conditions to afford the corresponding 2‐substituted arylbenzimidazole and arylbenzothiazole derivatives in good to excellent yields. This procedure constitutes a simple and practical green synthetic method for 2‐arylbenzimidazoles and 2‐arylbenzothiazoles and their structural analogs. Furthermore, the catalyst can be reused for several times but it will be less active. © 2009 Wiley Periodicals, Inc. Heteroatom Chem 20:202–207, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/hc.20534
- 31 January 2008
- Published by Elsevier in Chinese Journal of Catalysis
- Vol. 29 (1) , 10-14
Cu3/2PMo12O40/SiO2: A Heterogeneous, Eco-friendly and Reusable Catalyst for the Solvent-Free Catalytic Preparation of 1,1-Diacetates from Aldehydes
- 31 January 2008
- Published by Elsevier in Chinese Journal of Catalysis
- Vol. 29 (1) , 10-14
Cu3/2PMo12O40/SiO2: A Heterogeneous, Eco-friendly and Reusable Catalyst for the Solvent-Free Catalytic Preparation of 1,1-Diacetates from Aldehydes