| Ambient synthesis of spiro [4H-pyran-oxindole] derivatives under [BMIm] BF4 catalysis K Rad-Moghadam, L Youseftabar-Miri Tetrahedron 67 (31), 5693-5699, 2011 | 116 | 2011 |
| Synthesis of symmetrical and unsymmetrical 3, 3-di (indolyl) indolin-2-ones under controlled catalysis of ionic liquids K Rad-Moghadam, M Sharifi-Kiasaraie, H Taheri-Amlashi Tetrahedron 66 (13), 2316-2321, 2010 | 107 | 2010 |
| Green fabrication of Cu/pistachio shell nanocomposite using Pistacia Vera L. hull: An efficient catalyst for expedient reduction of 4-nitrophenol and organic dyes A Taghizadeh, K Rad-Moghadam Journal of Cleaner Production 198, 1105-1119, 2018 | 78 | 2018 |
| Mg (BF4) 2 doped in [BMIm][BF4]: A homogeneous ionic liquid-catalyst for efficient synthesis of 1, 8-dioxo-octahydroxanthenes, decahydroacridines and 14-aryl-14H-dibenzo [a, j … K Rad-Moghadam, SC Azimi Journal of Molecular Catalysis A: Chemical 363, 465-469, 2012 | 78 | 2012 |
| Synthesis of novel pyrano[3,2-c]quinoline-2,5-diones using an acidic ionic liquid catalyst K Rad-Moghadam, SC Azimi, E Abbaspour-Gilandeh Tetrahedron Letters 54 (35), 4633-4636, 2013 | 64 | 2013 |
| Indole 3-alkylation/vinylation under catalysis of the guanidinium ionic liquids K Rad-Moghadam, M Sharifi-Kiasaraie Tetrahedron 65 (43), 8816-8820, 2009 | 56 | 2009 |
| Tetramethylguanidinium triflate: An efficient catalyst solvent for the convergent synthesis of fused spiro [1, 4-dihydropyridine-oxindole] compounds K Rad-Moghadam, L Youseftabar-Miri Journal of Fluorine Chemistry 135, 213-219, 2012 | 45 | 2012 |
| An unexpected multicomponent reaction leading to 2-arylpyrrolo[2,3,4-kl]acridin-1(2H)-ones H Kefayati, F Narchin, K Rad-Moghadam Tetrahedron Letters 53 (34), 4573-4575, 2012 | 42 | 2012 |
| An expeditious and one-pot synthesis of unsymmetrical 2, 5-disubstituted-1, 3, 4-oxadiazoles under microwave irradiation and solvent-free conditions N Montazeri, K Rad-Moghadam Chinese Chemical Letters 19 (10), 1143-1146, 2008 | 41 | 2008 |
| A Facile Synthesis of 6-Substituted Benzimidazo[1,2-c]-Quinazolines Under Microwave Irradiation MS Khajavi, K Rad-Moghadam, H Hazarkhani Synthetic communications 29 (15), 2617-2624, 1999 | 37 | 1999 |
| A four-component synthesis of novel spiro [pyrazoloquinoline-oxindoles] under solvent-free conditions H Hosseinjani-Pirdehi, K Rad-Moghadam, L Youseftabar-Miri Tetrahedron 70 (9), 1780-1785, 2014 | 34 | 2014 |
| Synthesis of novel oxindolylpyrrolo[2,3-d]pyrimidines via a three-component sequential tandem reaction K Rad-Moghadam, SC Azimi Tetrahedron 68 (47), 9706-9712, 2012 | 33 | 2012 |
| One‐pot three‐component synthesis of 2‐substituted 4‐aminoquinazolines K Rad‐Moghadam, L Samavi Journal of heterocyclic chemistry 43 (4), 913-916, 2006 | 33 | 2006 |
| An Expeditious and Solvent-Free Route to the Synthesis of 2-Substituted Quinazolin-4(3H)-Ones Under Microwave Conditions K Rad-Moghadam, M Mohseni Journal of Chemical Research 2003 (8), 487-488, 2003 | 30 | 2003 |
| N-methyl-2-pyrrolidonium chlorosulfonate: an efficient ionic-liquid catalyst and mild sulfonating agent for one-pot synthesis of δ-sultones K Rad-Moghadam, SARM Hassani, ST Roudsari Journal of Molecular Liquids 218, 275-280, 2016 | 29 | 2016 |
| Synthesis of 4-substituted pyrano[4,3-b]pyran-2,5-diones in an ionic liquid K Rad-Moghadam, M Sharifi-Kiasaraie, SC Azimi Tetrahedron 68 (32), 6472-6476, 2012 | 29 | 2012 |
| A route to the synthesis of novel coumarins K Rad-Moghadam, M Mohseni Monatshefte für Chemie/Chemical Monthly 135, 817-821, 2004 | 27 | 2004 |
| A novel biginelli-like reaction: An efficient one-pot synthesis of spiro [oxindole-quinazoline/pyrimidine] ones H Kefayati, K Rad-Moghadam, M Zamani, S Hosseyni Letters in Organic Chemistry 7 (4), 277, 2010 | 25 | 2010 |
| One-pot Synthesis of Substituted Quinazolin-4 (3 H)-ones under Microwave Irradiation MS Khajavi Journal of Chemical Research, Synopses, 702-703, 1998 | 25 | 1998 |
| Efficient catalytic application of a binary ionic liquid mixture in the synthesis of novel spiro [4 H-pyridine-oxindoles] SY Kalurazi, K Rad-Moghadam, S Moradi New Journal of Chemistry 41 (18), 10291-10298, 2017 | 23 | 2017 |
