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Volumn 15, Issue 1, 2011, Pages 239-243

One-pot synthesis of benzochromeno-pyrazole derivatives

Author keywords

Naphthol; Naphthol; 3 Methyl 1H pyrazol 5(4H) one; Benzochromeno pyrazole derivatives; Multicomponent reaction

Indexed keywords

1 NAPHTHOL; 11 (4 CHLOROPHENYL) 13 METHYL 17 OXA 14,15 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),13 HEPTAENE; 11 (4 FLUOROPHENYL) 13 METHYL 17 OXA 14,15 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),13 HEPTAENE; 11 (FURAN 2 YL) 13 METHYL 17 OXA 14,15 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),13 HEPTAENE; 11 ETHYL 13 METHYL 17 OXA 14,15 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),13 HEPTAENE; 13 METHYL 11 (3 NITROPHENYL) 17 OXA 14,15 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),13 HEPTAENE; 13 METHYL 11 (4 NITROPHENYL) 17 OXA 14,15 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1 (10),2(7),3,5,8,12(16), 13 HEPTAENE; 13 METHYL 11 (NAPHTHALENE 1 YL) 17 OXA 14,15 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),13 HEPTAENE; 13 METHYL 11 [(E) 2 PHENYLETHENYL] 17 OXA 14,15 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),13 HEPTAENE; 15 METHYL 17 (4 METHYLPHENYL) 11 OXA 13,14 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),14 HEPTAENE; 15 METHYL 17 (4 NITROPHENYL) 11 OXA 13,14 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),14 HEPTAENE; 15 METHYL 17 (NAPHTHALEN 1 YL) 11 OXA 13,14 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),14 HEPTAENE; 15,17 DIMETHYL 11 OXA 13,14 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),14 HEPTAENE; 17 (4 METHOXYPHENYL) 15 METHYL 11 OXA 13,14 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),14 HEPTAENE; 2 NAPHTHOL; 3 METHYL 1H PYRAZOL 5 (4H) ONE; 4 [15 METHYL 11 OXA 13,14 DIAZATETRACYCLO[8.7.0.0 2,7.0 12,16]HEPTADECA 1(10),2(7),3,5,8,12(16),14 HEPTAENE 17-YL]PHENOL; ALDEHYDE; BENZOCHROMENO PYRAZOLE DERIVATIVE; CHEMICAL COMPOUND; PYRAZOLE; PYRAZOLE DERIVATIVE; SOLVENT; SULFAMIC ACID; SULFUR ACID AMIDE; UNCLASSIFIED DRUG;

EID: 79953313809     PISSN: 13811991     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11030-010-9263-4     Document Type: Article
Times cited : (17)

References (17)
  • 1
    • 0036603766 scopus 로고    scopus 로고
    • Recent advances in isocyanide-based multicomponent chemistry
    • doi:10.1016/S1367-5931(02)00328-9
    • Dömling A (2002) Recent advances in isocyanide-based multicomponent chemistry. Curr Opin Chem Biol 6:303-313. doi:10.1016/S1367-5931(02)00328-9
    • (2002) Curr Opin Chem Biol , vol.6 , pp. 303-313
    • Dömling, A.1
  • 2
    • 49949152144 scopus 로고    scopus 로고
    • Isocyanide-based multicomponent reactions in drug discovery
    • doi:10.1016/j.cbpa.2008.02.004
    • Akritopoulou-Zanze I (2008) Isocyanide-based multicomponent reactions in drug discovery. Curr Opin Chem Biol 12:324-331. doi:10.1016/j.cbpa.2008.02.004
    • (2008) Curr Opin Chem Biol , vol.12 , pp. 324-331
    • Akritopoulou-Zanze, I.1
  • 3
    • 0033019939 scopus 로고    scopus 로고
    • Discovery of new multi component reactions with combinatorial methods
    • Weber L, Illgen K, Almstetter M (1999) Discovery of new multi component reactions with combinatorial methods. Synlett 366-374. doi:10.1055/s-1999-2612 (Pubitemid 29125486)
    • (1999) Synlett , Issue.3 , pp. 366-374
    • Weber, L.1    Illgen, K.2    Almstetter, M.3
  • 4
    • 0034665244 scopus 로고    scopus 로고
    • Maximizing synthetic efficiency: Multi-component transformations lead the way
    • doi:10.1002/1521-3765(20000915)6:18〈3321
    • Bienayme H, Hulme C, Oddon G, Schmitt P (2000) Maximizing synthetic efficiency: multi-component transformations lead the way. Chem Eur J 6:3321-3329. doi:10.1002/1521-3765(20000915)6:18〈3321
    • (2000) Chem Eur J , vol.6 , pp. 3321-3329
    • Bienayme, H.1    Hulme, C.2    Oddon, G.3    Schmitt, P.4
  • 5
    • 33745585548 scopus 로고    scopus 로고
    • Application of multicomponent reactions to antimalarial drug discovery. Part 2: New antiplasmodial and antitrypanosomal 4-aminoquinoline gamma and deltalactams via a 'catch and release' protocol
    • doi:10.1016/j.bmc.2006.04.035
    • Musonda CC, Gut J, Rosenthal PJ, Yardley V, Souza RCC, de Chibale K (2006) Application of multicomponent reactions to antimalarial drug discovery. Part 2: New antiplasmodial and antitrypanosomal 4-aminoquinoline gamma and deltalactams via a 'catch and release' protocol. Bioorg Med Chem 14:5605-5615. doi:10.1016/j.bmc.2006.04.035
    • (2006) Bioorg Med Chem , vol.14 , pp. 5605-5615
    • Musonda, C.C.1    Gut, J.2    Rosenthal, P.J.3    Yardley, V.4    Souza, R.C.C.5    De Chibale, K.6
  • 7
    • 84944053241 scopus 로고    scopus 로고
    • In comprehensive heterocyclic chemistry
    • Katritzky AR, Rees CW, Scriven EFV (eds) 1st edn. Pergamon, New York
    • Geen GR, Evans JM, Vong AK (1996) In comprehensive heterocyclic chemistry. In: Katritzky AR, Rees CW, Scriven EFV (eds) Comprehensive heterocyclic chemistry, vol 5, 1st edn. Pergamon, New York, pp 469-500
    • (1996) Comprehensive Heterocyclic Chemistry , vol.5 , pp. 469-500
    • Geen, G.R.1    Evans, J.M.2    Vong, A.K.3
  • 9
    • 66549116590 scopus 로고    scopus 로고
    • Comprehensive modulation of naphthopyran photochromism in a rigid host matrix by applying polymer conjugation
    • doi:10.1021/ma801947d
    • Ercole F, Davis TP, Evans RA (2009) Comprehensive modulation of naphthopyran photochromism in a rigid host matrix by applying polymer conjugation. Macromolecule 42:1500-1511. doi:10.1021/ma801947d
    • (2009) Macromolecule , vol.42 , pp. 1500-1511
    • Ercole, F.1    Davis, T.P.2    Evans, R.A.3
  • 12
    • 69049090144 scopus 로고    scopus 로고
    • Synthesis and antimicrobial evaluation of some new pyrazole, pyrazoline and chromeno[3,4-c]pyrazole derivatives
    • doi:10.1590/S0103-50532009000500024
    • Abunada NM, Hassaneen HM, Samaha AMSA, Miqdad OA (2009) Synthesis and antimicrobial evaluation of some new pyrazole, pyrazoline and chromeno[3,4-c]pyrazole derivatives. J Braz Chem Soc 20:975-987. doi:10.1590/S0103-50532009000500024
    • (2009) J Braz Chem Soc , vol.20 , pp. 975-987
    • Abunada, N.M.1    Hassaneen, H.M.2    Samaha, A.M.S.A.3    Miqdad, O.A.4
  • 13
    • 58149093267 scopus 로고    scopus 로고
    • A novel three-component reaction for the synthesis of N-cyclohexyl-3-aryl-quinoxaline-2-amines
    • doi:10.1016/j.tetlet.2008.11.123
    • Heravi MM, Baghernejad B, Oskooie HA (2009) A novel three-component reaction for the synthesis of N-cyclohexyl-3-aryl-quinoxaline-2-amines. Tetrahedron Lett 50:767-769. doi:10.1016/j.tetlet.2008.11.123
    • (2009) Tetrahedron Lett , vol.50 , pp. 767-769
    • Heravi, M.M.1    Baghernejad, B.2    Oskooie, H.A.3
  • 14
    • 50849126505 scopus 로고    scopus 로고
    • A novel and facile synthesis of 2-(cyclohexylamino)-6,7-dihydro-3-aryl- 1Hindole-4(5H)-ones via a one-pot multi-component reaction
    • doi:10.1016/j.tetlet.2008.08.012
    • Heravi MM, Baghernejad B, Oskooie HA, Hekmatshoar R (2008) A novel and facile synthesis of 2-(cyclohexylamino)-6,7-dihydro-3-aryl-1Hindole-4(5H)-ones via a one-pot multi-component reaction. Tetrahedron Lett 49:6101-6103. doi:10.1016/j.tetlet.2008.08.012
    • (2008) Tetrahedron Lett , vol.49 , pp. 6101-6103
    • Heravi, M.M.1    Baghernejad, B.2    Oskooie, H.A.3    Hekmatshoar, R.4
  • 15
    • 77954314425 scopus 로고    scopus 로고
    • Onepot three-component synthesis of the spiroacenaphthylene derivatives
    • doi:10.1016/j.tet.2010.05.067
    • Saeedi M, Heravi MM, Beheshtiha YS, Oskooie HA (2010) Onepot three-component synthesis of the spiroacenaphthylene derivatives. Tetrahedron 66:5345-5348. doi:10.1016/j.tet.2010.05.067
    • (2010) Tetrahedron , vol.66 , pp. 5345-5348
    • Saeedi, M.1    Heravi, M.M.2    Beheshtiha, Y.S.3    Oskooie, H.A.4
  • 16
    • 78650180331 scopus 로고    scopus 로고
    • Sulfamic acid catalyzed solvent-free synthesis of 10-aryl-7,7-dimethyl- 6,7,8,10-tetrahydro-9H-[1,3]-dioxolo[4,5-b]xanthen-9-ones and 12-aryl-9, 9-dimethyl-8, 9, 10, 12-tetrahydro-11H-benzo[a]xanthen-11-ones
    • doi:10.1007/s11030-009-9196-y
    • Heravi MM, Alinejhad H, Bakhtiari K, Oskooie HA (2010) Sulfamic acid catalyzed solvent-free synthesis of 10-aryl-7,7-dimethyl- 6,7,8,10-tetrahydro- 9H-[1,3]-dioxolo[4,5-b]xanthen-9-ones and 12-aryl-9, 9-dimethyl-8, 9, 10, 12-tetrahydro-11H-benzo[a]xanthen-11-ones. Mol Divers. doi:10.1007/s11030-009- 9196-y
    • (2010) Mol Divers
    • Heravi, M.M.1    Alinejhad, H.2    Bakhtiari, K.3    Oskooie, H.A.4
  • 17
    • 70349971948 scopus 로고    scopus 로고
    • Application of sulfamic acid in organic synthesis - A short review
    • doi:10.2174/138527209788680790
    • Heravi MM, Baghernejad B, Oskooie HA (2009) Application of sulfamic acid in organic synthesis - a short review. Curr Org Chem 13:1002-1014. doi:10.2174/138527209788680790
    • (2009) Curr Org Chem , vol.13 , pp. 1002-1014
    • Heravi, M.M.1    Baghernejad, B.2    Oskooie, H.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.