Roya Jahanshahi
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Roya Jahanshahi has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
- Batool Akhlaghinia
Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, Mashhad 9177948974, Iran
8 shared publications - Jose Miguel Sansano
Departamento de Química Orgánica and Instituto de Síntesis Orgánica (ISO), Universidad de Alicante, Apdo. 99, E-03080 Alicante, Spain
2 shared publications Sara Sobhani
Dep. Chem., Coll. Sci., Univ. Birjand, Birjand 414, Iran
2 shared publications- Sara Sobhani
Department of Chemistry, College of Sciences University of Birjand Birjand Iran
2 shared publications Alireza Paseban
Department of Chemistry, College of Sciences, University of Birjand, Birjand, Iran
1 shared publication- Asma Khazaee
Department of Chemistry, College of Sciences, University of Birjand, Birjand, Iran
1 shared publication
Latest Publications
- Open Access
- 2 October 2025
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 15 (44) , 36823-36836
MOF modified with a Cu-complex as a novel MOF-based heterogeneous catalyst for the one-pot one-step synthesis of α-aminophosphonates directly from alcohols by a tandem oxidation process
Cu-ISA-MIL-Fe successfully catalyzes the direct one-pot synthesis of dialkyl α-aminophosphonates from alcohols via a tandem oxidation process (TOP). The catalyst offers high efficiency and excellent recyclability for sustainable synthesis.
- 2 October 2025
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 15 (44) , 36823-36836
Open AccessMOF modified with a Cu-complex as a novel MOF-based heterogeneous catalyst for the one-pot one-step synthesis of α-aminophosphonates directly from alcohols by a tandem oxidation process
Cu-ISA-MIL-Fe successfully catalyzes the direct one-pot synthesis of dialkyl α-aminophosphonates from alcohols via a tandem oxidation process (TOP). The catalyst offers high efficiency and excellent recyclability for sustainable synthesis.
- 27 July 2020
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 44 (37) , 15871-15886
Design and synthesis of aptamer AS1411-conjugated EG@TiO2@Fe2O3nanoparticles as a drug delivery platform for tumor-targeted therapy
AS1411@GMBS@EG@TiO2@Fe2O3nanoparticle is an effective and safe pH-responsive sustained release system for targeted drug delivery into nucleolin-positive cells.
- 27 July 2020
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 44 (37) , 15871-15886
Design and synthesis of aptamer AS1411-conjugated EG@TiO2@Fe2O3nanoparticles as a drug delivery platform for tumor-targeted therapy
AS1411@GMBS@EG@TiO2@Fe2O3nanoparticle is an effective and safe pH-responsive sustained release system for targeted drug delivery into nucleolin-positive cells.
- 10 June 2020
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 44 (27) , 11513-11526
g-C 3 N 4 /γ-Fe 2 O 3 /TiO 2 /Pd: a new magnetically separable photocatalyst for visible-light-driven fluoride-free Hiyama and Suzuki–Miyaura cross-coupling reactions at room temperature
G-C 3 N 4 /γ-Fe 2 O 3 /TiO 2 /Pd is developed as a new magnetically separable photocatalyst for efficient fluoride-free Hiyama and Suzuki–Miyaura cross-coupling reactions at room temperature under visible light irradiation.
- 10 June 2020
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 44 (27) , 11513-11526
g-C 3 N 4 /γ-Fe 2 O 3 /TiO 2 /Pd: a new magnetically separable photocatalyst for visible-light-driven fluoride-free Hiyama and Suzuki–Miyaura cross-coupling reactions at room temperature
G-C 3 N 4 /γ-Fe 2 O 3 /TiO 2 /Pd is developed as a new magnetically separable photocatalyst for efficient fluoride-free Hiyama and Suzuki–Miyaura cross-coupling reactions at room temperature under visible light irradiation.
- 28 December 2017
- Published by Springer Nature in Research on Chemical Intermediates
- Vol. 44 (4) , 2451-2474
Heteropolyacid anchored on SBA-15 functionalized with 2-aminoethyl dihydrogen phosphate: a novel and highly efficient catalyst for one-pot, three-component synthesis of trisubstituted 1,3-thiazoles
- 28 December 2017
- Published by Springer Nature in Research on Chemical Intermediates
- Vol. 44 (4) , 2451-2474
Heteropolyacid anchored on SBA-15 functionalized with 2-aminoethyl dihydrogen phosphate: a novel and highly efficient catalyst for one-pot, three-component synthesis of trisubstituted 1,3-thiazoles
- 15 June 2017
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 41 (15) , 7203-7219
Cu( ii )-grafted SBA-15 functionalized S-methylisothiourea aminated epibromohydrin (SBA-15/E-SMTU-Cu II ): a novel and efficient heterogeneous mesoporous catalyst
The catalytic activity of novel synthesized SBA-15/E-SMTU-Cu II nanocatalyst was investigated for the green, one-pot, pseudo five-component synthesis of tetrahydropyridine derivatives.
- 15 June 2017
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 41 (15) , 7203-7219
Cu( ii )-grafted SBA-15 functionalized S-methylisothiourea aminated epibromohydrin (SBA-15/E-SMTU-Cu II ): a novel and efficient heterogeneous mesoporous catalyst
The catalytic activity of novel synthesized SBA-15/E-SMTU-Cu II nanocatalyst was investigated for the green, one-pot, pseudo five-component synthesis of tetrahydropyridine derivatives.
- 24 February 2017
- Published by Springer Nature in Journal of Chemical Sciences
- Vol. 129 (3) , 313-328
Green and efficient synthesis of aryl/alkylbis(indolyl)methanes using Expanded Perlite-PPA as a heterogeneous solid acid catalyst in aqueous media
- 24 February 2017
- Published by Springer Nature in Journal of Chemical Sciences
- Vol. 129 (3) , 313-328
Green and efficient synthesis of aryl/alkylbis(indolyl)methanes using Expanded Perlite-PPA as a heterogeneous solid acid catalyst in aqueous media
- 27 December 2016
- Published by Springer Nature in Catalysis Letters
- Vol. 147 (2) , 360-373
Aminophosphine Palladium(0) Complex Supported on ZrO2 Nanoparticles (ZrO2@AEPH2-PPh2-Pd(0)) as an Efficient Heterogeneous Catalyst for Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media
- 27 December 2016
- Published by Springer Nature in Catalysis Letters
- Vol. 147 (2) , 360-373
Aminophosphine Palladium(0) Complex Supported on ZrO2 Nanoparticles (ZrO2@AEPH2-PPh2-Pd(0)) as an Efficient Heterogeneous Catalyst for Suzuki–Miyaura and Heck–Mizoroki Reactions in Green Media
- 3 November 2016
- Published by Wiley in ChemInform
- Vol. 47 (47)
ChemInform Abstract: Direct Access to Stabilized CuI Using Cuttlebone as a Natural-Reducing Support for Efficient CuAAC Click Reactions in Water.
The reaction is conducted under environmentally benign conditions.
- 3 November 2016
- Published by Wiley in ChemInform
- Vol. 47 (47)
ChemInform Abstract: Direct Access to Stabilized CuI Using Cuttlebone as a Natural-Reducing Support for Efficient CuAAC Click Reactions in Water.
The reaction is conducted under environmentally benign conditions.