メンバー|PEOPLE

Arash Ghaderi

Postdoctoral Researcher

2023.09-

 

Education

• Ph. D. in Organic Chemistry, Shiraz University (Sept 23, 2007Jan 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

Silica gel catalyzed highly selective C–S bond formation via Michael addition of thiols to α, β-unsaturated ketones under solvent-free conditions

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]

 

ZrOCl2·8H2O as a highly efficient and the moisture tolerant Lewis acid catalyst for Michael addition of amines and indoles to α, β-unsaturated ketones under solvent-free conditions

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]

 

ZrOCl2·8H2O/silica gel as a new efficient and a highly water–tolerant catalyst system for facile condensation of indoles with carbonyl compounds under solvent-free conditions

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]

 

Silica sulfuric acid as an efficient catalyst for the Friedlander quinoline synthesis from simple ketones and ortho-amino aryl ketones under microwave irradiation

Mohammad Ali Zolfigol,* Peyman Salehi, Morteza Shiri, Toktam Rastegar, Arash Ghaderi

J. Iran. Chem. Soc. 2008, 5, 490–497. (DOI: 10.1007/BF03246007) [PDF]

 

Highly efficient halogenation of organic compounds with halides catalyzed by cerium(III) chloride heptahydrate using hydrogen peroxide as the terminal oxidant in water

Habib Firouzabadi,* Nasser Iranpoor,* Somayeh Kazemi, Arash Ghaderi, Atefeh Garzan

Adv. Synth. Catal. 2009, 351, 1925–1932. (DOI: 10.1002/adsc.200900124) [PDF]

 

Palladium nanoparticles supported on aminopropyl functionalized clay as efficient catalysts for phosphine-free C–C bond formation via Mizoroki–Heck and Suzuki–Miyaura reactions

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]

 

Gelatin as a bioorganic reductant, ligand and support for palladium nanoparticles. Application as a catalyst for ligand- and amine-free Sonogashira-Hagihara reaction

Habib Firouzabadi,* Nasser Iranpoor,* Arash Ghaderi

Org. Biomol. Chem. 2011, 9, 865–871. (DOI: 10.1039/c0ob00253d) [PDF]

 

Solvent-free Mizoroki-Heck reaction catalyzed by palladium nano-particles deposited on gelatin as the reductant, ligand and the non-toxic and degradable natural product support

Habib Firouzabadi,* Nasser Iranpoor,* Arash Ghaderi

J. Mol. Catal. A: Chem. 2011, 347, 38–45. (DOI: 10.1016/j.molcata.2011.07.008) [PDF]

 

Cerium (IV) oxide as a neutral catalyst for aldehyde-induced decarboxylative coupling of L-proline with triethyl phosphite and nitromethane

Habib Firouzabadi,* Nasser Iranpoor,* Arash Ghaderi, Maryam Ghavami

Tetrahedron Lett. 2012, 53, 5515–5518. (DOI: 10.1016/j.tetlet.2012.08.012) [PDF]

 

Nickel-catalyzed coupling of thiomethyl-substituted 1,3-benzothiazoles with secondary alkyl Grignard reagents

Arash Ghaderi, Takanori Iwasaki, Asuka Fukuoka, Jun Terao, Nobuaki Kambe*

Chem. Eur. J. 2013, 19, 2951–2955. (DOI: 10.1002/chem.201203413) [PDF]

 

Palladium nanoparticles supported on gum arabic as a reusable catalyst for solvent-free Mizoroki-Heck reaction

Ardeshir Khazaei,* Sadegh Rahmati,* Arash Ghaderi, Leila Roshani

J. Iran. Chem. Soc. 2014, 11, 263–269. (DOI: 10.1007/s13738-013-0296-3) [PDF]

 

Design and synthesis of a new phosphinite-functionalized clay composite for the stabilization of palladium nanoparticles. Application as a recoverable catalyst for C–C bond formation reactions

Habib Firouzabadi,* Nasser Iranpoor,* Arash Ghaderi, Mohammad Gholinejad, Sajjad Rahimi, Safura Jokar

RSC Adv. 2014, 4, 27674–27682. (DOI: 10.1039/c4ra03645j) [PDF]

 

Ligand-free Cu-catalyzed odorless synthesis of unsymmetrical sulfides through cross-coupling reaction of aryl/benzyl/alkyl halides with an aryl boronic acid/S8 system as a thiolating agent in PEG

Abed Rostami, Amin Rostami,* Arash Ghaderi, Mohammad Ali Zolfigol

RSC Adv. 2015, 5, 37060–37065. (DOI: 10.1039/c5ra05244k) [PDF]

 

Copper-catalyzed thioetherification reactions of alkyl halides, triphenyltin chloride and arylboronic acids with nitroarenes in the presence of sulfur sources

Abed Rostami, Amin Rostami,* Arash Ghaderi*

J. Org. Chem. 2015, 80, 8694–8704. (DOI: 10.1021/acs.joc.5b01248) [PDF]

 

Palladium supported on phosphinite functionalized Fe3O4 nanoparticles as a new magnetically separable catalyst for Suzuki-Miyaura coupling reaction in aqueous media

Mohammad Gholinejad,* Mehran Razeghi, Arash Ghaderi,* Pullithadathil Biji

Catal. Sci. Technol. 2016, 6, 3117–3127. (DOI: 10.1039/c5cy00821b) [PDF]

 

Palladium deposited on naturally occurring supports as a powerful catalyst for carbon-carbon bond formation reactions

Arash Ghaderi, Mohammad Gholinejad, Habib Firouzabadi

Curr. Org. Chem. 2016, 20, 327–348. [PDF]

 

Advances in transition-metal catalyzed thioetherification reactions of aromatic compounds

Arash Ghaderi*

Tetrahedron 2016, 72, 4758–4782. (DOI: 10.1016/j.tet.2016.06.067) [PDF]

 

Copper-catalyzed C–S bond formation via the cleavage of C–O bonds in the presence of S8 as the sulfur source

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]

 

Pivalic acid-assisted Rh(III)-catalyzed C–H functionalization of 2-arylpyridine derivatives using arylsilanes

Arash Ghaderi, Takanori Iwasaki, Nobuaki Kambe*

Asian J. Org. Chem. 2019, 8, 1344–1347. (DOI: 10.1002/ajoc.201900362) [PDF]

 

Copper-catalyzed demethylative esterification of arylmethylketones: A new route for the synthesis of benzocaine

Sajedeh Maddah Roodan, Arash Ghaderi*

J. Iran. Chem. Soc. 2019, 16, 2327–2332. (DOI: 10.1007/s13738-019-01698-z) [PDF]

 

Metal-free aerobic oxidative esterification of aromatic aldehydes promoted by potassium fluoride (KF)

Roghaye Soltani, Arash Ghaderi*

J. Chin. Chem. Soc. 2019, 66, 1572–1576. (DOI: 10.1002/jccs.201800344) [PDF]

 

Light-emitting diode light-enabled denitrative etherification of 4-nitrobenzonitrile under catalyst-free conditions at room temperature

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]

 

Eco-friendly foul release coatings based on a novel reduced graphene oxide/Ag nanocomposite prepared by a green synthesis approach

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]

 

2-Aryl-perfluorobenzoxazoles: Synthesis, fluorescence properties and synthetic application in cubic platinum nanoparticles

Rong Wang, Hao Lu, Mingpan Yan, Mengfan Li, Xiangyu Lv, Hongwen Huang, Arash Ghaderi, Takanori Iwasaki, Nobuaki Kambe,* Ablimit Abdukader,* Renhua Qiu*

J. Mater. Chem. C 2021, 9, 12545–12549. (DOI: 10.1039/d1tc03338g) [PDF]

 

Nickel- and palladium-catalyzed cross-coupling of stibines with organic halides: site-selective sequential reactions with polyhalogenated arenes

Dejiang Zhang, Ting Tang, Zhao Zhang, Liyuan Le, Zhi Xu, Hao Lu, Zhou Tong, Dishu Zeng, Wai-Yeung Wong,* Shuang-Feng Yin,* Arash Ghaderi, Nobuaki Kambe,* Renhua Qiu*

ACS Catal. 2022, 12, 854–867. (DOI: 10.1021/acscatal.1c04533) [PDF]

 

Synthesis of N-sulfonylimidines via three-component reaction of proline, aldehydes, and sulfonyl azides under metal-free conditions

Fattaneh Mohammadpour, Arash Ghaderi*

Monatshefte für Chemie-Chemical Monthly 2022, 153, 487–494. (DOI: 10.1007/s00706-022-02914-y) [PDF]

 

Corrosion inhibition of a novel antihistamine-based compound for mild steel in hydrochloric acid solution: Experimental and computational studies

Mohammad Ghaderi, Ahmad Ramazani S. A.,* Azadeh Kordzadeh, Mohammad Mahdavian,* Eiman Alibakhshi, Arash Ghaderi

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]

THE NOYORI LABORATORY | 野依特別研究室 名古屋大学 大学院理学研究科 野依特別研究室 / 名古屋大学 物質科学国際研究センター 分子触媒研究分野 〒464-8602 名古屋市千種区不老町 名古屋大学 野依記念物質科学研究館 http://noy.chem.nagoya-u.ac.jp/

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