메뉴 건너뛰기




Volumn 17, Issue 3, 2013, Pages 459-469

Catalyst-free, one-pot, three-component synthesis of 5-amino-1,3-aryl-1- pyrazole-4-carbonitriles in green media

Author keywords

5 Amino pyrazole; Catalyst free; Green chemistry; MCRs; Multi component reactions; Pyrazole

Indexed keywords

3,3' (1,3 PHENYLENE)BIS(5 AMINO 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE); 3,3' (1,4 PHENYLENE)BIS(5 AMINO 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE); 5 AMINO 1 (4 BROMOPHENYL) 3 (NAPHTHALEN 1 YL)1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 1 (4 BROMOPHENYL) 3 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 1 (4 CHLOROPHENYL) 3 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 1 PHENYL 3 (THIOPHEN 2 YL) 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 1 PHENYL 3 P TOLYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 1,3 DIPHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 1,3 DIPHENYL 1H PYRAZOLE 4 CARBOXYLATE; 5 AMINO 3 (2 HYDROXYPHENYL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 3 (2 NITROPHENYL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 3 (3 NITROPHENYL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 3 (3,4 DIMETHOXYPHENYL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 3 (4 CHLOROPHENYL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 3 (4 CYANOPHENYL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 3 (4 ETHOXYPHENYL) 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 3 (4 ISOPROPYLPHENYL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 3 (4 NITROPHENYL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 3 (5 METHYLTHIOPHEN 2 YL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5 AMINO 3 (NAPHTHALENE 6 YL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRILE; 5' AMINO 2 OXO 1' PHENYL 1',2' DIHYDROSPIRO[INDOLINE 3,3' PYRAZOLE] 4 CARBONITRILE; ANTIBIOTIC AGENT; ANTIFUNGAL AGENT; ANTINEOPLASTIC AGENT; CYANIDE; DIETHYL 3,3' (1,4 PHENYLENE)BIS(5 AMINO 1 PHENYL 1H PYRAZOLE 4 CARBOXYLATE); METHYL 5 AMINO 1,3 DIPHENYL 1H PYRAZOLE 4 CARBOXYLATE; METHYL 5 AMINO 3 (4 NITROPHENYL) 1 PHENYL 1H PYRAZOLE 4 CARBONITRATE; PYRAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84880807933     PISSN: 13811991     EISSN: 1573501X     Source Type: Journal    
DOI: 10.1007/s11030-013-9445-y     Document Type: Article
Times cited : (38)

References (66)
  • 1
    • 79953833571 scopus 로고    scopus 로고
    • Sulfuric acid-modified PEG-6000 (PEG-OSO3H): An efficient, bio-degradable and reusable polymeric catalyst for the solvent-free synthesis of poly-substituted quinolines under microwave irradiation
    • 10.1039/c0gc00953a 10.1039/c0gc00953a 1:CAS:528:DC%2BC3MXkt1Khsbs%3D
    • Hasaninejad A, Zare A, Shekouhy M (2011) Sulfuric acid-modified PEG-6000 (PEG-OSO3H): an efficient, bio-degradable and reusable polymeric catalyst for the solvent-free synthesis of poly-substituted quinolines under microwave irradiation. Green Chem 13:958-964. doi: 10.1039/c0gc00953a
    • (2011) Green Chem , vol.13 , pp. 958-964
    • Hasaninejad, A.1    Zare, A.2    Shekouhy, M.3
  • 2
    • 78149304818 scopus 로고    scopus 로고
    • Catalyst-free one-pot four component synthesis of polysubstituted imidazoles in neutral. Ionic liquid 1-butyl-3-methylimidazolium bromide
    • 10.1021/cc100097m 20828194 10.1021/cc100097m 1:CAS:528:DC%2BC3cXhtFegsrrL
    • Hasaninejad A, Zare A, Shekouhy M (2010) Catalyst-free one-pot four component synthesis of polysubstituted imidazoles in neutral. Ionic liquid 1-butyl-3-methylimidazolium bromide. J Comb Chem 12:844-849. doi: 10.1021/cc100097m
    • (2010) J Comb Chem , vol.12 , pp. 844-849
    • Hasaninejad, A.1    Zare, A.2    Shekouhy, M.3
  • 3
    • 77955131155 scopus 로고    scopus 로고
    • Lithium bromide as an efficient, green, and inexpensive catalyst for the synthesis of quinoxaline derivatives at room temperature
    • 10.1080/17518251003619192 10.1080/17518251003619192 1:CAS:528: DC%2BC3cXhtlSntrjL
    • Hasaninejad A, Zare A, Mohammadizadeh MR, Shekouhy M (2010) Lithium bromide as an efficient, green, and inexpensive catalyst for the synthesis of quinoxaline derivatives at room temperature. Green Chem Lett Rev 3:143-148. doi: 10.1080/17518251003619192
    • (2010) Green Chem Lett Rev , vol.3 , pp. 143-148
    • Hasaninejad, A.1    Zare, A.2    Mohammadizadeh, M.R.3    Shekouhy, M.4
  • 4
    • 78650176189 scopus 로고    scopus 로고
    • Highly efficient synthesis of triazolo[1,2-a]indazole-triones and novel spiro triazolo[1,2-a]indazole-tetraones under solvent-free conditions
    • 10.1016/j.tet.2010.11.029 10.1016/j.tet.2010.11.029
    • Hasaninejad A, Zare A, Shekouhy M (2010) Highly efficient synthesis of triazolo[1,2-a]indazole-triones and novel spiro triazolo[1,2-a]indazole- tetraones under solvent-free conditions. Tetrahedron 67:390-400. doi: 10.1016/j.tet.2010.11.029
    • (2010) Tetrahedron , vol.67 , pp. 390-400
    • Hasaninejad, A.1    Zare, A.2    Shekouhy, M.3
  • 5
    • 61849138988 scopus 로고    scopus 로고
    • Zirconium Tetrakis(dodecyl Sulfate) [Zr(DS)4] as an efficient Lewis acid-surfactant combined catalyst for the synthesis of quinoxaline derivatives in aqueous media
    • 10.1080/00397910802406737 10.1080/00397910802406737 1:CAS:528: DC%2BD1MXhtFSgsLg%3D
    • Hasaninejad A, Zare A, Zolfigol MA, Shekouhy M (2009) Zirconium Tetrakis(dodecyl Sulfate) [Zr(DS)4] as an efficient Lewis acid-surfactant combined catalyst for the synthesis of quinoxaline derivatives in aqueous media. Synth Commun 39:569-579. doi: 10.1080/00397910802406737
    • (2009) Synth Commun , vol.39 , pp. 569-579
    • Hasaninejad, A.1    Zare, A.2    Zolfigol, M.A.3    Shekouhy, M.4
  • 6
    • 83455230765 scopus 로고    scopus 로고
    • Diversity-oriented synthesis of novel 2′-aminospiro[11-indeno[1,2- b]quinoxaline-11,4′-[4H] pyran] derivatives via a one-pot four-component reaction
    • 10.1002/hlca.201100201 10.1002/hlca.201100201 1:CAS:528: DC%2BC3MXhsF2ltLbO
    • Hasaninejad A, Golzar N, Shekouhy M, Zare A (2011) Diversity-oriented synthesis of novel 2′-aminospiro[11-indeno[1,2-b]quinoxaline-11,4′- [4H] pyran] derivatives via a one-pot four-component reaction. Helv Chim Acta 94:2289-2294. doi: 10.1002/hlca.201100201
    • (2011) Helv Chim Acta , vol.94 , pp. 2289-2294
    • Hasaninejad, A.1    Golzar, N.2    Shekouhy, M.3    Zare, A.4
  • 7
    • 83455236687 scopus 로고    scopus 로고
    • Silica nanoparticles efficiently catalyzed synthesis of quinolines andquinoxalines
    • 10.1039/c1cy00332a 10.1039/c1cy00332a 1:CAS:528:DC%2BC3MXhsF2js73E
    • Hasaninejad A, Shekouhy M, Zare A (2012) Silica nanoparticles efficiently catalyzed synthesis of quinolines andquinoxalines. Catal Sci Technol 2:201-214. doi: 10.1039/c1cy00332a
    • (2012) Catal Sci Technol , vol.2 , pp. 201-214
    • Hasaninejad, A.1    Shekouhy, M.2    Zare, A.3
  • 8
    • 4544336251 scopus 로고    scopus 로고
    • In vivo radioprotection of mice by 3-methyl-1-phenyl-2-pyrazolin-5-one (Edaravone; Radicut), a clinical drug
    • 15304976 10.1269/jrr.45.319 1:CAS:528:DC%2BD2cXot1OqtL0%3D
    • Anzai K, Furuse M, Yoshida A, Matsuyama A, Moritake T, Tsuboi K, Ikota N (2004) In vivo radioprotection of mice by 3-methyl-1-phenyl-2-pyrazolin-5-one (Edaravone; Radicut), a clinical drug. J Radiat Res 45:319-323
    • (2004) J Radiat Res , vol.45 , pp. 319-323
    • Anzai, K.1    Furuse, M.2    Yoshida, A.3    Matsuyama, A.4    Moritake, T.5    Tsuboi, K.6    Ikota, N.7
  • 9
    • 84879499655 scopus 로고    scopus 로고
    • Katritzky AR, Ramsden CA, Scriven EFV, Taylor RJK (eds.). Elsevier, Oxford
    • Yet L (2008) in Comprehensive heterocyclic chemistry III. In: Katritzky AR, Ramsden CA, Scriven EFV, Taylor RJK (eds.). Elsevier, Oxford 4:1
    • (2008) Comprehensive Heterocyclic Chemistry III , vol.4 , pp. 1
    • Yet, L.1
  • 10
    • 0032104228 scopus 로고    scopus 로고
    • Antimicrobial and antineoplastic activities of new 4-diazopyrazole derivatives
    • doi: 10.1016/S0223-5234(98)80004-4
    • Daidone G, Maggio B, Plescia S, Raffa D, Musiu C, Milia C, Perra G, Marongiu ME (1998) Antimicrobial and antineoplastic activities of new 4-diazopyrazole derivatives. Eur J Med Chem 33:375-382. doi: 10.1016/S0223-5234(98)80004-4
    • (1998) Eur J Med Chem , vol.33 , pp. 375-382
    • Daidone, G.1    Maggio, B.2    Plescia, S.3    Raffa, D.4    Musiu, C.5    Milia, C.6    Perra, G.7    Marongiu, M.E.8
  • 11
    • 0026671082 scopus 로고
    • Synthesis of pyrazolo 3,4-dpyrimidine analogues of the potent agent N-4-2-2-amino-4 3H-oxo-7H-pyrrolo 2,3-dpyrimidin-5-yl ethylbenzoyl-L-glutamic acid (LY231514)
    • 10.1016/S0040-4020(01)80479-8 10.1016/S0040-4020(01)80479-8 1:CAS:528:DyaK3sXntlCn
    • Taylor EC, Patel H, Kumar H (1992) Synthesis of pyrazolo 3,4-dpyrimidine analogues of the potent agent N-4-2-2-amino-4 3H-oxo-7H-pyrrolo 2,3-dpyrimidin-5-yl ethylbenzoyl-L-glutamic acid (LY231514). Tetrahedron 48:8089-8100. doi: 10.1016/S0040-4020(01)80479-8
    • (1992) Tetrahedron , vol.48 , pp. 8089-8100
    • Taylor, E.C.1    Patel, H.2    Kumar, H.3
  • 12
    • 12344301275 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of 4-benzoyl-1-methyl-5-phenyl-1- pyrazole-3-carboxylic acid and derivatives
    • 10.1016/j.farmac.2004.09.003 15652364 10.1016/j.farmac.2004.09.003 1:CAS:528:DC%2BD2MXisF2mug%3D%3D
    • Akbas E, Berber I, Sener A, Hasanov B (2005) Synthesis and antibacterial activity of 4-benzoyl-1-methyl-5-phenyl-1-pyrazole-3-carboxylic acid and derivatives. IL Farmaco 60:23-26. doi: 10.1016/j.farmac.2004.09.003
    • (2005) IL Farmaco , vol.60 , pp. 23-26
    • Akbas, E.1    Berber, I.2    Sener, A.3    Hasanov, B.4
  • 13
    • 2342485135 scopus 로고    scopus 로고
    • Design, synthesis and structure-activity relationship studies of novel indazole analogues as DNA gyrase inhibitors with Gram-positive antibacterial activity
    • 10.1016/j.bmcl.2004.03.044 15125947 10.1016/j.bmcl.2004.03.044 1:CAS:528:DC%2BD2cXjs1amtbo%3D
    • Tanitame A, Oyamada Y, Ofuji K (2004) Design, synthesis and structure-activity relationship studies of novel indazole analogues as DNA gyrase inhibitors with Gram-positive antibacterial activity. Bioorg Med Chem Lett 14:2857-2862. doi: 10.1016/j.bmcl.2004.03.044
    • (2004) Bioorg Med Chem Lett , vol.14 , pp. 2857-2862
    • Tanitame, A.1    Oyamada, Y.2    Ofuji, K.3
  • 14
    • 1642461641 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of some pyrazole derivatives as anti-inflammatory-antimicrobial agents
    • 10.1016/j.bmc.2004.01.037 10.1016/j.bmc.2004.01.037
    • Bekhita AA, Abdel-Aziem T (2004) Design, synthesis and biological evaluation of some pyrazole derivatives as anti-inflammatory-antimicrobial agents. Bioorg Med Chem 12:1935-1945. doi: 10.1016/j.bmc.2004.01.037
    • (2004) Bioorg Med Chem , vol.12 , pp. 1935-1945
    • Bekhita, A.A.1    Abdel-Aziem, T.2
  • 15
    • 0000593527 scopus 로고
    • Studies on the hemorrhagic sweet clover disease: V. identification and synthesis of hemorrhagic agent
    • Stahman MA, Huebner CF, Link KP (1941) Studies on the hemorrhagic sweet clover disease: v. identification and synthesis of hemorrhagic agent. J Biol Chem 138:513-527
    • (1941) J Biol Chem , vol.138 , pp. 513-527
    • Stahman, M.A.1    Huebner, C.F.2    Link, K.P.3
  • 16
    • 0031722425 scopus 로고    scopus 로고
    • Antibacterials and antimycotics: Part 1: Synthesis and activity of 2-pyrazoline derivatives
    • 9734312 10.1248/cpb.46.1254 1:CAS:528:DyaK1cXlsFyjur4%3D
    • Nauduri D, Reddy GB (1998) Antibacterials and antimycotics: part 1: synthesis and activity of 2-pyrazoline derivatives. Chem Pharm Bull 46:1254-1260
    • (1998) Chem Pharm Bull , vol.46 , pp. 1254-1260
    • Nauduri, D.1    Reddy, G.B.2
  • 17
    • 21744458419 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of 1H-pyrazolo[3,4-b]pyrazine and -pyridine derivatives
    • 10.1016/j.farmac.2005.05.002 15950227 10.1016/j.farmac.2005.05.002 1:CAS:528:DC%2BD2MXlvFKqt7o%3D
    • Foks H, Pancechowska-Ksepko D, Kedzia A, Zwolska Z, Janowiec M, Augustynowicz-Kopec E (2005) Synthesis and antibacterial activity of 1H-pyrazolo[3,4-b]pyrazine and -pyridine derivatives. IL Farmaco 60:513-517. doi: 10.1016/j.farmac.2005.05.002
    • (2005) IL Farmaco , vol.60 , pp. 513-517
    • Foks, H.1    Pancechowska-Ksepko, D.2    Kedzia, A.3    Zwolska, Z.4    Janowiec, M.5    Augustynowicz-Kopec, E.6
  • 19
    • 33749265829 scopus 로고    scopus 로고
    • Pyrazolidine-3,5-diones and 5-hydroxy-1-pyrazol-3(2-ones, Inhibitors of UDP- N-acetylenolpyruvyl glucosamine reductase
    • 10.1021/jm060499t 10.1021/jm060499t
    • Gilbert AM, Failli A, Shumsky J, Yang Y (2006) Pyrazolidine-3,5-diones and 5-hydroxy-1-pyrazol-3(2-ones, Inhibitors of UDP- N-acetylenolpyruvyl glucosamine reductase. J Med Chem 49:1202-1204. doi: 10.1021/jm060499t
    • (2006) J Med Chem , vol.49 , pp. 1202-1204
    • Gilbert, A.M.1    Failli, A.2    Shumsky, J.3    Yang, Y.4
  • 20
    • 3042552189 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of a novel series of potent DNA gyrase inhibitors. Pyrazole derivatives
    • doi: 10.1021/jm030394f
    • Tanitame A, Oyamada Y, Ofugi K, Fujimoto M, Iwai N, Hiyama Y, Suzuki KM, Yamagishi J (2004) Synthesis and antibacterial activity of a novel series of potent DNA gyrase inhibitors. Pyrazole derivatives. J Med Chem 47:3693-3696. doi: 10.1021/jm030394f
    • (2004) J Med Chem , vol.47 , pp. 3693-3696
    • Tanitame, A.1    Oyamada, Y.2    Ofugi, K.3    Fujimoto, M.4    Iwai, N.5    Hiyama, Y.6    Suzuki, K.M.7    Yamagishi, J.8
  • 21
    • 0032102385 scopus 로고    scopus 로고
    • Nonsteroidal antiinflammatory agents - Part 1: Antiinflammatory, analgesic and antipyretic activity of some new 1-(pyrimidin-2-yl)-3-pyrazolin-5- ones and 2-(pyrimidin-2-yl)-1,2,4,5,6,7-hexahydro-3-indazol-3-ones
    • 10.1016/S0223-5234(98)80002-0 10.1016/S0223-5234(98)80002-0 1:CAS:528:DyaK1cXjvFKqtLY%3D
    • Badawey AM, El-Ashmawey IM (1998) Nonsteroidal antiinflammatory agents - part 1: antiinflammatory, analgesic and antipyretic activity of some new 1-(pyrimidin-2-yl)-3-pyrazolin-5-ones and 2-(pyrimidin-2-yl)-1,2,4,5,6,7- hexahydro-3-indazol-3-ones. Eur J Med Chem 33:349-361. doi: 10.1016/S0223- 5234(98)80002-0
    • (1998) Eur J Med Chem , vol.33 , pp. 349-361
    • Badawey, A.M.1    El-Ashmawey, I.M.2
  • 22
    • 0035105126 scopus 로고    scopus 로고
    • 5-disubstituted-3-methyl-1H-pyrazolo[3,4-c]pyridazines
    • doi: 10.1016/S0968-0896(00)00285-6
    • 5-disubstituted-3-methyl-1H-pyrazolo[3,4-c] pyridazines. Bioorg Med Chem 9:715-718. doi: 10.1016/S0968-0896(00)00285-6
    • (2001) Bioorg Med Chem , vol.9 , pp. 715-718
    • Tewari, A.K.1    Mishra, A.2
  • 24
    • 0342368828 scopus 로고    scopus 로고
    • Synthesis and preliminary evaluation of new 5-pyrazolinone derivatives as analgesic agents
    • S0223523400001173/FLA 10785562 10.1016/S0223-5234(00)00117-3 1:CAS:528:DC%2BD3cXis1Wns7Y%3D
    • Gursoy SA, Demirayak G, Capan K (2000) Synthesis and preliminary evaluation of new 5-pyrazolinone derivatives as analgesic agents. Eur J Med Chem 35:359-364. doi: S0223523400001173/FLA
    • (2000) Eur J Med Chem , vol.35 , pp. 359-364
    • Gursoy, S.A.1    Demirayak, G.2    Capan, K.3
  • 26
    • 33847411932 scopus 로고    scopus 로고
    • Synthesis and studies on antidepressant and anticonvulsant activities of some 3-(2-furyl)-pyrazoline derivatives
    • 10.1016/j.ejmech.2006.09.006 17069933 10.1016/j.ejmech.2006.09.006
    • Özdemir Z, Kandilci HB, Gümüsel B, Calis Ü, Bilgin AA (2007) Synthesis and studies on antidepressant and anticonvulsant activities of some 3-(2-furyl)-pyrazoline derivatives. Eur J Med Chem 42:373-379. doi: 10.1016/j.ejmech.2006.09.006
    • (2007) Eur J Med Chem , vol.42 , pp. 373-379
    • Özdemir, Z.1    Kandilci, H.B.2    Gümüsel, B.3    Calis, Ü.4    Bilgin, A.A.5
  • 27
    • 0027074210 scopus 로고
    • 4H-thieno[3,4-c]pyrazole derivatives with antiinflammatory, analgesic, antipyretic and platelet antiaggregating activities
    • Menozzi G, Mosti L, Schenone P, D-Amico M, Filippelli A, Rossi F (1992) 4H-thieno[3,4-c]pyrazole derivatives with antiinflammatory, analgesic, antipyretic and platelet antiaggregating activities. Farmaco 47:1495-1511
    • (1992) Farmaco , vol.47 , pp. 1495-1511
    • Menozzi, G.1    Mosti, L.2    Schenone, P.3    D-Amico, M.4    Filippelli, A.5    Rossi, F.6
  • 28
    • 0037205947 scopus 로고    scopus 로고
    • 1,3-Diphenylpyrazoles: Synthesis and antiparasitic activities of azomethine derivatives
    • doi: 10.1016/S0223-5234(02)01388-0
    • Rathelot P, Azas N, El-Kashef H, Delmas F (2002) 1,3-Diphenylpyrazoles: synthesis and antiparasitic activities of azomethine derivatives. Eur J Med Chem 37:671-679. doi: 10.1016/S0223-5234(02)01388-0
    • (2002) Eur J Med Chem , vol.37 , pp. 671-679
    • Rathelot, P.1    Azas, N.2    El-Kashef, H.3    Delmas, F.4
  • 29
    • 33244494206 scopus 로고    scopus 로고
    • Synthesis and leishmanicidal activities of 1-(4-X-phenyl)-N′-[(4-Y- phenyl)methylene]-1-pyrazole-4-carbohydrazides
    • doi: 10.1016/j.ejmech.2005.10.007
    • Bernardino AMR, Gomes AO, Charret KS, Freitas ACC (2006) Synthesis and leishmanicidal activities of 1-(4-X-phenyl)-N′-[(4-Y-phenyl)methylene]-1- pyrazole-4-carbohydrazides. Eur J Med Chem 41:80-87. doi: 10.1016/j.ejmech.2005. 10.007
    • (2006) Eur J Med Chem , vol.41 , pp. 80-87
    • Amr, B.1    Gomes, A.O.2    Charret, K.S.3    Acc, F.4
  • 30
    • 25844500311 scopus 로고    scopus 로고
    • Synthesis of 2-[3,5-substituted pyrazol-1-yl]-4,6-trisubstituted triazine derivatives as antimalarial agents
    • doi: 10.1016/j.bmcl.2005.08.023
    • Katiyar SB, Srivastava K, Purib SK, Chauhana PMS (2005) Synthesis of 2-[3,5-substituted pyrazol-1-yl]-4,6-trisubstituted triazine derivatives as antimalarial agents. Bioorg Med Chem Lett 15: 4957-4960. doi: 10.1016/j.bmcl.2005.08.023
    • (2005) Bioorg Med Chem Lett , vol.15 , pp. 4957-4960
    • Katiyar, S.B.1    Srivastava, K.2    Purib, S.K.3    Pms, C.4
  • 31
    • 78649335610 scopus 로고    scopus 로고
    • Design, synthesis and structure-activity relationship study of novel pyrazole-based heterocycles as potential antitumor agents
    • 10.1016/j.ejmech.2010.09.054 20950898 10.1016/j.ejmech.2010.09.054 1:CAS:528:DC%2BC3cXhsVGit7%2FE
    • Farag AM, Ali KA, Mayhoub AS, Abdalla TM, Amr AE, Abdel-Hafez N, Abdalla MM (2010) Design, synthesis and structure-activity relationship study of novel pyrazole-based heterocycles as potential antitumor agents. Eur J Med Chem 45:5887-5898. doi: 10.1016/j.ejmech.2010.09.054
    • (2010) Eur J Med Chem , vol.45 , pp. 5887-5898
    • Farag, A.M.1    Ali, K.A.2    Mayhoub, A.S.3    Abdalla, T.M.4    Amr, A.E.5    Abdel-Hafez, N.6    Abdalla, M.M.7
  • 32
    • 0036171878 scopus 로고    scopus 로고
    • Synthesis and biological activity of some 4-substituted 1-[1-(2,3-dihydroxy-1-propoxy)methyl-1,2,3-triazol-(4 & 5)-ylmethyl]-1- pyrazolo[3,4-]pyrimidines
    • doi: 10.1016/S0014-827X(01)01152-1
    • Moukha-Chafiq O, Taha ML, Lazrek HB, Vasseur JJ (2002) Synthesis and biological activity of some 4-substituted 1-[1-(2,3-dihydroxy-1-propoxy)methyl- 1,2,3-triazol-(4 & 5)-ylmethyl]-1-pyrazolo[3,4-]pyrimidines. IL Farmaco 57:27-32. doi: 10.1016/S0014-827X(01)01152-1
    • (2002) IL Farmaco , vol.57 , pp. 27-32
    • Moukha-Chafiq, O.1    Taha, M.L.2    Lazrek, H.B.3    Vasseur, J.J.4
  • 33
    • 30344476416 scopus 로고    scopus 로고
    • Synthesis of C-6 substituted pyrazolo[1,5-a]pyridines with potent activity against herpesviruses
    • 10.1016/j.bmc.2005.09.015 16213142 10.1016/j.bmc.2005.09.015 1:CAS:528:DC%2BD28XhvFOitw%3D%3D
    • Allen SH, Johns BA, Gudmundsson KS, Freeman GA (2006) Synthesis of C-6 substituted pyrazolo[1,5-a]pyridines with potent activity against herpesviruses. Bioorg Med Chem 14:944-954. doi: 10.1016/j.bmc.2005.09.015
    • (2006) Bioorg Med Chem , vol.14 , pp. 944-954
    • Allen, S.H.1    Johns, B.A.2    Gudmundsson, K.S.3    Freeman, G.A.4
  • 34
    • 38449091148 scopus 로고    scopus 로고
    • Synthesis and biological activities of novel bis-heterocyclic pyrrodiazole derivatives
    • doi: 10.1002/hc.20369
    • He FQ, Liu XH, Wang BL, Li ZM (2008) Synthesis and biological activities of novel bis-heterocyclic pyrrodiazole derivatives. Heteroatom Chemistry 19:21-27. doi: 10.1002/hc.20369
    • (2008) Heteroatom Chemistry , vol.19 , pp. 21-27
    • He, F.Q.1    Liu, X.H.2    Wang, B.L.3    Li, Z.M.4
  • 35
    • 0030833652 scopus 로고    scopus 로고
    • Synthesis and insecticidal activity of novel pyrazole methanesulfonates
    • 10.1002/(SICI)1096-9063(199708) 10.1002/(SICI)1096-9063(199708)50: 4<324: AID-PS596>3.0.CO;2-D
    • Frinkelstein BL, Strok CJ (1997) Synthesis and insecticidal activity of novel pyrazole methanesulfonates. J Pestic Sci 50:324-328. doi: 10.1002/(SICI)1096-9063(199708)
    • (1997) J Pestic Sci , vol.50 , pp. 324-328
    • Frinkelstein, B.L.1    Strok, C.J.2
  • 36
    • 0032434638 scopus 로고    scopus 로고
    • Synthesis of pyrazolecarbonylaminopyridinecarboxamides as herbicides
    • 10.1002/jhet.5570350646 10.1002/jhet.5570350646 1:CAS:528: DyaK1MXltFSksQ%3D%3D
    • Parlow JJ (1998) Synthesis of pyrazolecarbonylaminopyridinecarboxamides as herbicides. J Heterocycl Chem 35:1493-1499. doi: 10.1002/jhet.5570350646
    • (1998) J Heterocycl Chem , vol.35 , pp. 1493-1499
    • Parlow, J.J.1
  • 37
    • 66549126873 scopus 로고    scopus 로고
    • Pyrazoles and pyrazolides-flexible synthons in self-assembly
    • doi: 10.1039/B815577A
    • Halcrow MA (2009) Pyrazoles and pyrazolides-flexible synthons in self-assembly. Dalton Trans 2059-2073: doi: 10.1039/B815577A
    • (2009) Dalton Trans , pp. 2059-2073
    • Ma, H.1
  • 38
    • 33646077886 scopus 로고    scopus 로고
    • Development of nonproprietary phosphine ligands for the Pd-catalyzed amination reaction
    • 10.1016/j.tetlet.2006.03.132 10.1016/j.tetlet.2006.03.132 1:CAS:528:DC%2BD28Xkt1yitrk%3D
    • Singer RA, Dore M, Sieser JE, Berliner MA (2006) Development of nonproprietary phosphine ligands for the Pd-catalyzed amination reaction. Tetrahedron Lett 47:3727-3731. doi: 10.1016/j.tetlet.2006.03.132
    • (2006) Tetrahedron Lett , vol.47 , pp. 3727-3731
    • Singer, R.A.1    Dore, M.2    Sieser, J.E.3    Berliner, M.A.4
  • 39
    • 0344495989 scopus 로고    scopus 로고
    • Ureas of 5-aminopyrazole and 2-aminothiazole inhibit growth of gram-positive bacteria
    • doi: 10.1016/j.bmcl.2003.09.013
    • Kane JL, Hirth BH, Laing O, Gourlie BB, Nahill S, Barsomiam G (2003) Ureas of 5-aminopyrazole and 2-aminothiazole inhibit growth of gram-positive bacteria. Bioorg Med Chem Lett 13: 4463-4466. doi: 10.1016/j.bmcl.2003.09.013
    • (2003) Bioorg Med Chem Lett , vol.13 , pp. 4463-4466
    • Kane, J.L.1    Hirth, B.H.2    Laing, O.3    Gourlie, B.B.4    Nahill, S.5    Barsomiam, G.6
  • 40
    • 25444505339 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of some new 1-heteroaryl-5-amino-4- phenyl-3-trifluoromethylpyrazoles
    • 10.1016/j.ejmech.2005.03.021 15921826 10.1016/j.ejmech.2005.03.021 1:CAS:528:DC%2BD2MXhtVCltLzE
    • Kumar V, Aggarwal R, Tyagi P, Singh SP (2005) Synthesis and antibacterial activity of some new 1-heteroaryl-5-amino-4-phenyl-3-trifluoromethylpyrazoles. Eur J Med Chem 40:922-927. doi: 10.1016/j.ejmech.2005.03.021
    • (2005) Eur J Med Chem , vol.40 , pp. 922-927
    • Kumar, V.1    Aggarwal, R.2    Tyagi, P.3    Singh, S.P.4
  • 42
    • 0030572496 scopus 로고    scopus 로고
    • TM), a potent and selective inhibitor of type 5 cGMP phosphodiesterase with utility for the treatment of male erectile dysfunction
    • doi: 10.1016/0960-894X(96)00323-X
    • TM), a potent and selective inhibitor of type 5 cGMP phosphodiesterase with utility for the treatment of male erectile dysfunction. Bioorg Med Chem Lett 6:1819-1824. doi: 10.1016/0960-894X(96)00323-X
    • (1996) Bioorg Med Chem Lett , vol.6 , pp. 1819-1824
    • Terrett, N.K.1    Bell, A.S.2    Brown, D.3    Ellis, P.4
  • 45
    • 0034624679 scopus 로고    scopus 로고
    • Novel 1,5-diphenylpyrazole nonnucleoside HIV-1 reverse transcriptase inhibitors with enhanced activity versus the delavirdine-resistant P236L mutant:? lead identification and SAR of 3- and 4-substituted derivatives
    • 10.1021/jm990383f
    • Genin MJ, Biles C, Keiser BJ, Poppe SM, Swaney SM, Tarpley WG, Yagi Y, Romero DL (2000) Novel 1,5-diphenylpyrazole nonnucleoside HIV-1 reverse transcriptase inhibitors with enhanced activity versus the delavirdine-resistant P236L mutant:? lead identification and SAR of 3- and 4-substituted derivatives. J Med Chem 43:904-909. doi: 10.1021/jm990383f
    • (2000) J Med Chem , vol.43 , pp. 904-909
    • Genin, M.J.1    Biles, C.2    Keiser, B.J.3    Poppe, S.M.4    Swaney, S.M.5    Tarpley, W.G.6    Yagi, Y.7    Romero, D.L.8
  • 46
    • 0038298270 scopus 로고    scopus 로고
    • Regioselective synthesis of ethyl pyrazolecarboxylates from ethyl 3-[(dimethylamino)methylidene]pyruvate and diethyl 3-[(dimethylamino) methylidene]-2-oxosuccinate. Isolation of ethyl 4,5-dihydro-1-heteroaryl-5- hydroxy-1 H -pyrazole-5-carboxylates as stable intermediates in the pyrazole ring formation
    • 10.1002/jhet.5570400313 10.1002/jhet.5570400313 1:CAS:528: DC%2BD3sXls1Kkuro%3D
    • Hanzlowsky A, Jelencic B, Recnik S, Svete J, Golobic A, Stanovnik B (2003) Regioselective synthesis of ethyl pyrazolecarboxylates from ethyl 3-[(dimethylamino)methylidene]pyruvate and diethyl 3-[(dimethylamino) methylidene]-2-oxosuccinate. Isolation of ethyl 4,5-dihydro-1-heteroaryl-5- hydroxy-1 H -pyrazole-5-carboxylates as stable intermediates in the pyrazole ring formation. J Heterocycl Chem 40:487-498. doi: 10.1002/jhet.5570400313
    • (2003) J Heterocycl Chem , vol.40 , pp. 487-498
    • Hanzlowsky, A.1    Jelencic, B.2    Recnik, S.3    Svete, J.4    Golobic, A.5    Stanovnik, B.6
  • 47
    • 11144220008 scopus 로고    scopus 로고
    • Pyrazol-3-ones. Part II: Reactions of the ring atoms
    • 10.1016/S0065-2725(04)87003-X 1:CAS:528:DC%2BD2MXhsVeksro%3D
    • Varvounis G, Fiamegos Y, Pilidis G (2004) Pyrazol-3-ones. Part II: reactions of the ring atoms. Adv Heterocycl Chem 87:141-272
    • (2004) Adv Heterocycl Chem , vol.87 , pp. 141-272
    • Varvounis, G.1    Fiamegos, Y.2    Pilidis, G.3
  • 48
    • 36048990067 scopus 로고    scopus 로고
    • N-Bromosuccinimide assisted oxidation of 5-aminopyrazoles: Formation of bis diazenylderivatives
    • 10.1016/j.tetlet.2007.10.079 10.1016/j.tetlet.2007.10.079 1:CAS:528:DC%2BD2sXhtlWku7fI
    • Salaheldin AM, Oliveira-Campos AMF, Rodrigues LM (2007) N-Bromosuccinimide assisted oxidation of 5-aminopyrazoles: formation of bis diazenylderivatives. Tetrahedron Lett 48:8819-8822. doi: 10.1016/j.tetlet.2007. 10.079
    • (2007) Tetrahedron Lett , vol.48 , pp. 8819-8822
    • Salaheldin, A.M.1    Oliveira-Campos, A.M.F.2    Rodrigues, L.M.3
  • 49
    • 37549069310 scopus 로고    scopus 로고
    • Pyrazol-3-ones. Part III: Reactivity of the ring substituents
    • 10.1016/S0065-2725(07)95002-3
    • Varvounis G, Fiamegos Y, Pilidis G (2007) Pyrazol-3-ones. Part III: reactivity of the ring substituents. Adv Heterocycl Chem 95:27-141
    • (2007) Adv Heterocycl Chem , vol.95 , pp. 27-141
    • Varvounis, G.1    Fiamegos, Y.2    Pilidis, G.3
  • 50
    • 69849103932 scopus 로고    scopus 로고
    • Recent advances in the synthesis of pyrazoles
    • doi: 10.1080/00304940903077832
    • Fustero S, Simon-Fuentes A, Sanz-Cervera JF (2009) Recent advances in the synthesis of pyrazoles. Org Prep Proced Int 41: 253-290. doi: 10.1080/00304940903077832
    • (2009) Org Prep Proced Int , vol.41 , pp. 253-290
    • Fustero, S.1    Simon-Fuentes, A.2    Sanz-Cervera, J.F.3
  • 51
    • 33746105769 scopus 로고    scopus 로고
    • 1,3-Diketones from acid chlorides and ketones: A rapid and general one-pot synthesis of pyrazoles
    • 10.1021/ol060570p 16774229 10.1021/ol060570p 1:CAS:528: DC%2BD28XltVCgsbo%3D
    • Heller ST, Natarajan SR (2006) 1,3-Diketones from acid chlorides and ketones: a rapid and general one-pot synthesis of pyrazoles. Org Lett 8:2675-2678. doi: 10.1021/ol060570p
    • (2006) Org Lett , vol.8 , pp. 2675-2678
    • Heller, S.T.1    Natarajan, S.R.2
  • 52
    • 0037533016 scopus 로고    scopus 로고
    • A novel one-pot method for the preparation of pyrazoles by 1,3-dipolar cycloadditions of diazo compounds generated in situ
    • 10.1021/jo0268409 12816503 10.1021/jo0268409 1:CAS:528: DC%2BD3sXjvFOiu78%3D
    • Aggarwal VK, Vicente J, Bonnert RV (2003) A novel one-pot method for the preparation of pyrazoles by 1,3-dipolar cycloadditions of diazo compounds generated in situ. J Org Chem 68:5381-5383. doi: 10.1021/jo0268409
    • (2003) J Org Chem , vol.68 , pp. 5381-5383
    • Aggarwal, V.K.1    Vicente, J.2    Bonnert, R.V.3
  • 53
    • 33750623389 scopus 로고    scopus 로고
    • Domino Cu-catalyzed C-N coupling/hydroamidation: A highly efficient synthesis of nitrogen heterocycles
    • 10.1002/anie.200602917 17009380 10.1002/anie.200602917 1:CAS:528:DC%2BD28Xht1ans7bO
    • Martin R, Rivero MR, Buchwald SL (2006) Domino Cu-catalyzed C-N coupling/hydroamidation: a highly efficient synthesis of nitrogen heterocycles. Angew Chem Int Ed Engl 45:7079-7082. doi: 10.1002/anie.200602917
    • (2006) Angew Chem Int Ed Engl , vol.45 , pp. 7079-7082
    • Martin, R.1    Rivero, M.R.2    Buchwald, S.L.3
  • 54
    • 78249271085 scopus 로고    scopus 로고
    • Efficient synthesis of pyrazoles: Oxidative C-C/N-N bond-formation cascade
    • doi: 10.1002/anie.201002389
    • Neumann JJ, Suri M, Glorius F (2010) Efficient synthesis of pyrazoles: oxidative C-C/N-N bond-formation cascade. Angew Chem Int Ed 49:903-907. doi: 10.1002/anie.201002389
    • (2010) Angew Chem Int Ed , vol.49 , pp. 903-907
    • Neumann, J.J.1    Suri, M.2    Glorius, F.3
  • 55
    • 4143104684 scopus 로고    scopus 로고
    • Copper-diamine-catalyzed N-arylation of pyrroles, pyrazoles, indazoles, imidazoles, and triazoles
    • 10.1021/jo049658b 15307726 10.1021/jo049658b 1:CAS:528: DC%2BD2cXlsFemu7s%3D
    • Antilla JC, Baskin JM, Barder TE, Buchwald SL (2004) Copper-diamine- catalyzed N-arylation of pyrroles, pyrazoles, indazoles, imidazoles, and triazoles. J Org Chem 69:5578-5587. doi: 10.1021/jo049658b
    • (2004) J Org Chem , vol.69 , pp. 5578-5587
    • Antilla, J.C.1    Baskin, J.M.2    Barder, T.E.3    Buchwald, S.L.4
  • 56
    • 1642479421 scopus 로고    scopus 로고
    • Mild conditions for copper-catalysed N-arylation of pyrazoles
    • 10.1021/jo049658b 10.1002/ejoc.200300709
    • Cristau HJ, Cellier PP, Spindler JF, Taillefer M (2004) Mild conditions for copper-catalysed N-arylation of pyrazoles. Eur J Org Chem 2004:695-709. doi: 10.1021/jo049658b
    • (2004) Eur J Org Chem , vol.2004 , pp. 695-709
    • Cristau, H.J.1    Cellier, P.P.2    Spindler, J.F.3    Taillefer, M.4
  • 57
    • 9644262708 scopus 로고    scopus 로고
    • Pyrazole-tethered arylphosphine ligands for Suzuki reactions of aryl chlorides: How important is chelation?
    • 10.1016/j.tetlet.2004.11.016 10.1016/j.tetlet.2004.11.016 1:CAS:528:DC%2BD2cXhtVCrur7E
    • Mukherjee A, Sarkar A (2004) Pyrazole-tethered arylphosphine ligands for Suzuki reactions of aryl chlorides: how important is chelation? Tetrahedron Lett 45:9525-9528. doi: 10.1016/j.tetlet.2004.11.016
    • (2004) Tetrahedron Lett , vol.45 , pp. 9525-9528
    • Mukherjee, A.1    Sarkar, A.2
  • 58
    • 35548982667 scopus 로고    scopus 로고
    • Simple copper salt-catalyzed N-arylation of nitrogen-containing heterocycles with aryl and heteroaryl halides
    • 10.1021/jo0712289 17902694 10.1021/jo0712289 1:CAS:528:DC%2BD2sXhtV2msLvN
    • Zhu L, Guo P, Li G, Lan J, Xie R, You J (2007) Simple copper salt-catalyzed N-arylation of nitrogen-containing heterocycles with aryl and heteroaryl halides. J Org Chem 72:8535-8538. doi: 10.1021/jo0712289
    • (2007) J Org Chem , vol.72 , pp. 8535-8538
    • Zhu, L.1    Guo, P.2    Li, G.3    Lan, J.4    Xie, R.5    You, J.6
  • 59
    • 41549126990 scopus 로고    scopus 로고
    • CuI/L (L=pyridine-functionalized 1,3-diketones) catalyzed C-N coupling reactions of aryl halides with NH-containing heterocycles
    • doi: 10.1016/j.tet.2008.02.082
    • Xi Z, Liu F, Zhou Y, Chen W (2008) CuI/L (L=pyridine-functionalized 1,3-diketones) catalyzed C-N coupling reactions of aryl halides with NH-containing heterocycles. Tetrahedron 64:4254-4259. doi: 10.1016/j.tet.2008. 02.082
    • (2008) Tetrahedron , vol.64 , pp. 4254-4259
    • Xi, Z.1    Liu, F.2    Zhou, Y.3    Chen, W.4
  • 60
    • 67749101415 scopus 로고    scopus 로고
    • C-H bonds as ubiquitous functionality: A general approach to complex arylated pyrazoles via sequential regioselective-arylation and N-alkylation enabled by SEM-group transposition
    • doi: 10.1021/ja8096114
    • Goikhman R, Jacques TL, Sames D (2009) C-H bonds as ubiquitous functionality: a general approach to complex arylated pyrazoles via sequential regioselective-arylation and N-alkylation enabled by SEM-group transposition. J Am Chem Soc 131:3042-3048. doi: 10.1021/ja8096114
    • (2009) J Am Chem Soc , vol.131 , pp. 3042-3048
    • Goikhman, R.1    Jacques, T.L.2    Sames, D.3
  • 61
    • 79960267903 scopus 로고    scopus 로고
    • Silica bonded n -propyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride (SB-DABCO): A highly efficient, reusable and new heterogeneous catalyst for the synthesis of 4 H -benzo[b] pyran derivatives
    • doi: 10.1016/j.apcata.2011.04.012
    • Hasaninejad A, Shekouhy M, Golzar N, Zare A, Doroodmand MM (2011) Silica bonded n -propyl-4-aza-1-azoniabicyclo[2.2.2]octane chloride (SB-DABCO): a highly efficient, reusable and new heterogeneous catalyst for the synthesis of 4 H -benzo[b] pyran derivatives. Appl Catal A: General 402:11-22. doi: 10.1016/j.apcata.2011.04.012
    • (2011) Appl Catal A: General , vol.402 , pp. 11-22
    • Hasaninejad, A.1    Shekouhy, M.2    Golzar, N.3    Zare, A.4    Doroodmand, M.M.5
  • 62
    • 84987490974 scopus 로고
    • Activated nitriles in heterocyclic synthesis: Novel syntheses of 3H-1,2,4-triazolo-[1,5-a]pyridine derivatives
    • 10.1002/hc.520060408 10.1002/hc.520060408 1:CAS:528:DyaK2MXntVWitro%3D
    • Aziz SI, Kandeel ZE, Husein MM, El-Gohary S, El-Maged EIA (1995) Activated nitriles in heterocyclic synthesis: Novel syntheses of 3H-1,2,4-triazolo-[1,5-a]pyridine derivatives. Heteroat Chem 6:319-323. doi: 10.1002/hc.520060408
    • (1995) Heteroat Chem , vol.6 , pp. 319-323
    • Aziz, S.I.1    Kandeel, Z.E.2    Husein, M.M.3    El-Gohary, S.4    El-Maged, E.I.A.5
  • 63
    • 79961077328 scopus 로고    scopus 로고
    • Highly selective synthesis of pyrazole and spiropyrazoline phosphonates via base-assisted reaction of the Bestmann Ohira reagent with Enones
    • doi: 10.1021/jo200582z
    • Verma D, Mobin S, Namboothiri INN (2011) Highly selective synthesis of pyrazole and spiropyrazoline phosphonates via base-assisted reaction of the Bestmann Ohira reagent with Enones. J Org Chem 76:4764-4770. doi: 10.1021/jo200582z
    • (2011) J Org Chem , vol.76 , pp. 4764-4770
    • Verma, D.1    Mobin, S.2    Inn, N.3
  • 64
    • 33947311765 scopus 로고
    • Oxidation by metal oxides. IV. Oxidation of organic compounds using nickel peroxide
    • 10.1021/jo01274a043 10.1021/jo01274a043 1:CAS:528:DyaF1cXltVKjt7s%3D
    • Balachandran KS, Bhatnagar I, George MV (1968) Oxidation by metal oxides. IV. Oxidation of organic compounds using nickel peroxide. J Org Chem 33:3891-3895. doi: 10.1021/jo01274a043
    • (1968) J Org Chem , vol.33 , pp. 3891-3895
    • Balachandran, K.S.1    Bhatnagar, I.2    George, M.V.3
  • 65
    • 0034618336 scopus 로고    scopus 로고
    • Regioselective synthesis of 1,3,5-triaryl-4-alkylpyrazoles: Novel ligands for the estrogen receptor
    • 10.1021/ol0062650 10964377 10.1021/ol0062650 1:CAS:528: DC%2BD3cXls1OkurY%3D
    • Huang YR, Katzenellenbogen JA (2000) Regioselective synthesis of 1,3,5-triaryl-4-alkylpyrazoles: novel ligands for the estrogen receptor. Org Lett 2:2833-2836. doi: 10.1021/ol0062650
    • (2000) Org Lett , vol.2 , pp. 2833-2836
    • Huang, Y.R.1    Katzenellenbogen, J.A.2
  • 66
    • 10844240709 scopus 로고    scopus 로고
    • Synthesis and relative stability of 3,5-diacyl-4,5-dihydro-1-pyrazoles prepared by dipolar cycloaddition of enones and -diazoketones
    • 10.1021/jo048741w 15609941 10.1021/jo048741w 1:CAS:528: DC%2BD2cXps1Onsrw%3D
    • Jung ME, Min SJ, Houk KN, Ess D (2004) Synthesis and relative stability of 3,5-diacyl-4,5-dihydro-1-pyrazoles prepared by dipolar cycloaddition of enones and -diazoketones. J Org Chem 69:9085-9089. doi: 10.1021/jo048741w
    • (2004) J Org Chem , vol.69 , pp. 9085-9089
    • Jung, M.E.1    Min, S.J.2    Houk, K.N.3    Ess, D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.