メンバー|PEOPLE
Arash Ghaderi
Postdoctoral Researcher
2023.09-
Education
• Ph. D. in Organic Chemistry, Shiraz University (Sept 23, 2007 – Jan 17, 2012), Shiraz, Iran.
Research supervisors: Prof. Habib Firouzabadi and Prof. Nasser Iranpoor
• M. Sc. in Organic Chemistry, Bu-Ali Sina University (Sept 23, 2005 – Sept 5, 2007), Hamadan, Iran.
Research supervisor: Prof. Mohammad Ali Zolfigol
• B. Sc. in Chemistry, Shiraz University (Sept 23, 2001 – Jul 1, 2005), Shiraz, Iran.
Publication
Habib Firouzabadi,* Nasser Iranpoor, Maasoumeh Jafarpour, Arash Ghaderi
J. Mol. Catal. A: Chem. 2006, 249, 98–102. (DOI: 10.1016/j.molcata.2006.01.004) [PDF]
Habib Firouzabadi,* Nasser Iranpoor, Maasoumeh Jafarpour, Arash Ghaderi
J. Mol. Catal. A: Chem. 2006, 252, 150–155. (DOI: 10.1016/j.molcata.2005.11.025) [PDF]
Habib Firouzabadi,* Nasser Iranpoor, Maasoumeh Jafarpour, Arash Ghaderi
J. Mol. Catal. A: Chem. 2006, 253, 249–251. (DOI: 10.1016/j.molcata.2006.03.043) [PDF]
An eco-friendly procedure for the synthesis of polysubstituted quinolines under aqueous media
Mohammad Ali Zolfigol,* Peyman Salehi, Arash Ghaderi, Morteza Shiri, Zahra Tanbakouchian
J. Mol. Catal. A: Chem. 2006, 259, 253–258. (DOI: 10.1016/j.molcata.2006.06.031) [PDF]
A catalytic and green procedure for Friedlander quinoline synthesis in aqueous media
Mohammad Ali Zolfigol,* Peyman Salehi, Arash Ghaderi, Morteza Shiri
Catal. Commun. 2007, 8, 1214–1218. (DOI: 10.1016/j.catcom.2006.11.004) [PDF]
Iodine-catalyzed Friedlander quinoline synthesis under solvent-free conditions
Mohammad Ali Zolfigol,* Peyman Salehi, Arash Ghaderi, Morteza Shiri
J. Chin. Chem. Soc. 2007, 54, 267–271. (DOI: 10.1002/jccs.200700039) [PDF]
Mohammad Ali Zolfigol,* Peyman Salehi, Morteza Shiri, Toktam Rastegar, Arash Ghaderi
J. Iran. Chem. Soc. 2008, 5, 490–497. (DOI: 10.1007/BF03246007) [PDF]
Habib Firouzabadi,* Nasser Iranpoor,* Somayeh Kazemi, Arash Ghaderi, Atefeh Garzan
Adv. Synth. Catal. 2009, 351, 1925–1932. (DOI: 10.1002/adsc.200900124) [PDF]
Habib Firouzabadi,* Nasser Iranpoor,* Arash Ghaderi, Maryam Ghavami, S. Jafar Hoseini
Bull. Chem. Soc. Jpn. 2011, 84, 100–109 [Highlighted in SYNFACTS 2011, 4, 450]. (DOI: 10.1246/bcsj.20100219) [PDF]
Habib Firouzabadi,* Nasser Iranpoor,* Arash Ghaderi
Org. Biomol. Chem. 2011, 9, 865–871. (DOI: 10.1039/c0ob00253d) [PDF]
Habib Firouzabadi,* Nasser Iranpoor,* Arash Ghaderi
J. Mol. Catal. A: Chem. 2011, 347, 38–45. (DOI: 10.1016/j.molcata.2011.07.008) [PDF]
Habib Firouzabadi,* Nasser Iranpoor,* Arash Ghaderi, Maryam Ghavami
Tetrahedron Lett. 2012, 53, 5515–5518. (DOI: 10.1016/j.tetlet.2012.08.012) [PDF]
Arash Ghaderi, Takanori Iwasaki, Asuka Fukuoka, Jun Terao, Nobuaki Kambe*
Chem. Eur. J. 2013, 19, 2951–2955. (DOI: 10.1002/chem.201203413) [PDF]
Ardeshir Khazaei,* Sadegh Rahmati,* Arash Ghaderi, Leila Roshani
J. Iran. Chem. Soc. 2014, 11, 263–269. (DOI: 10.1007/s13738-013-0296-3) [PDF]
RSC Adv. 2014, 4, 27674–27682. (DOI: 10.1039/c4ra03645j) [PDF]
Abed Rostami, Amin Rostami,* Arash Ghaderi, Mohammad Ali Zolfigol
RSC Adv. 2015, 5, 37060–37065. (DOI: 10.1039/c5ra05244k) [PDF]
Abed Rostami, Amin Rostami,* Arash Ghaderi*
J. Org. Chem. 2015, 80, 8694–8704. (DOI: 10.1021/acs.joc.5b01248) [PDF]
Mohammad Gholinejad,* Mehran Razeghi, Arash Ghaderi,* Pullithadathil Biji
Catal. Sci. Technol. 2016, 6, 3117–3127. (DOI: 10.1039/c5cy00821b) [PDF]
Arash Ghaderi, Mohammad Gholinejad, Habib Firouzabadi
Curr. Org. Chem. 2016, 20, 327–348. [PDF]
Advances in transition-metal catalyzed thioetherification reactions of aromatic compounds
Tetrahedron 2016, 72, 4758–4782. (DOI: 10.1016/j.tet.2016.06.067) [PDF]
Abed Rostami, Amin Rostami,* Arash Ghaderi,* Mohammad Gholinejad, Sajedeh Gheisarzadeh
Synthesis 2017, 49, 5025–5038. (DOI: 10.1055/s-0036-1588508) [PDF]
Nickel-catalyzed denitrative etherification of activated nitrobenzenes
Fatemeh Zamiran, Arash Ghaderi*
J. Iran. Chem. Soc. 2019, 16, 293–299. (DOI: 10.1007/s13738-018-1510-0) [PDF]
Arash Ghaderi, Takanori Iwasaki, Nobuaki Kambe*
Asian J. Org. Chem. 2019, 8, 1344–1347. (DOI: 10.1002/ajoc.201900362) [PDF]
Sajedeh Maddah Roodan, Arash Ghaderi*
J. Iran. Chem. Soc. 2019, 16, 2327–2332. (DOI: 10.1007/s13738-019-01698-z) [PDF]
Roghaye Soltani, Arash Ghaderi*
J. Chin. Chem. Soc. 2019, 66, 1572–1576. (DOI: 10.1002/jccs.201800344) [PDF]
Roghaye Soltani, Fatemeh Abdolladi, Arash Ghaderi*
J. Chem. Res. 2021, 56–59. (DOI: 10.1177/1747519820925376) [PDF]
Denitrative functionalization of nitroarenes
Sajedeh Maddah-Roodan, Roghaye Soltani, Arash Ghaderi
J. Iran. Chem. Soc. 2021, 18, 519–542. (DOI: 10.1007/s13738-020-02054-2) [PDF]
Soolmaz Soleimani, Ali Jannesari,* Morteza Yousefzadi, Arash Ghaderi, Adnan Shahdadi
Progress in Organic Coatings 2021, 151, 106107. (DOI: 10.1016/j.porgcoat.2020.106107) [PDF]
J. Mater. Chem. C 2021, 9, 12545–12549. (DOI: 10.1039/d1tc03338g) [PDF]
ACS Catal. 2022, 12, 854–867. (DOI: 10.1021/acscatal.1c04533) [PDF]
Fattaneh Mohammadpour, Arash Ghaderi*
Monatshefte für Chemie-Chemical Monthly 2022, 153, 487–494. (DOI: 10.1007/s00706-022-02914-y) [PDF]
Scientific Reports 2022, 12, 13450–13469. (DOI: 10.1038/s41598-022-17589-y) [PDF]
Copper-catalyzed synthesis of α-ketothioamides from ketones
Fatemeh Abdollahi, Arash Ghaderi*
J. Chin. Chem. Soc. 2023, 70, 949–955. (DOI: 10.1002/jccs.202200520) [PDF]