메뉴 건너뛰기




Volumn 142, Issue 11, 2011, Pages 1175-1180

Novel and chemoselective one-pot synthesis of 4-arylidene-2-phenyl-5(4H)- oxazolones starting from benzyl alcohols promoted by [(C14H 24N4)2W10O32]-[bmim] NO3

Author keywords

Aryl alcohol; Azlactone; Hybrid polyoxometalates; Ionic liquid; One pot synthesis

Indexed keywords


EID: 80054961163     PISSN: 00269247     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00706-011-0533-3     Document Type: Article
Times cited : (10)

References (32)
  • 1
    • 0000314051 scopus 로고
    • 10.1021/cr00038a013 1:CAS:528:DyaK2MXnvFegs70%3D
    • P Wipf 1995 Chem Rev 95 2115 10.1021/cr00038a013 1:CAS:528: DyaK2MXnvFegs70%3D
    • (1995) Chem Rev , vol.95 , pp. 2115
    • Wipf, P.1
  • 2
    • 0029278784 scopus 로고
    • 10.1039/np9951200135 1:CAS:528:DyaK2MXltFSis7Y%3D
    • JR Lewis 1995 Nat Prod Rep 12 135 10.1039/np9951200135 1:CAS:528:DyaK2MXltFSis7Y%3D
    • (1995) Nat Prod Rep , vol.12 , pp. 135
    • Lewis, J.R.1
  • 3
    • 0347063644 scopus 로고    scopus 로고
    • Muscarine, imidazole, oxazole, and thiazole alkaloids
    • DOI 10.1039/b304142p
    • Z Jin 2003 Nat Prod Rep 20 584 10.1039/b304142p 1:CAS:528: DC%2BD2cXpvVGiug%3D%3D (Pubitemid 38024763)
    • (2003) Natural Product Reports , vol.20 , Issue.6 , pp. 584-605
    • Jin, Z.1
  • 10
    • 0035252418 scopus 로고    scopus 로고
    • Stability of immobilized soybean lipoxygenases: Influence of coupling conditions on the ionization state of the active site Fe
    • DOI 10.1016/S0141-0229(00)00317-3, PII S0141022900003173
    • AC Chikere B Galunsky V Schünemann V Kasche 2001 Enzyme Microb Technol 28 168 10.1016/S0141-0229(00)00317-3 1:CAS:528:DC%2BD3MXptlSjtA%3D%3D (Pubitemid 32146635)
    • (2001) Enzyme and Microbial Technology , vol.28 , Issue.2-3 , pp. 168-175
    • Chikere, A.C.1    Galunsky, B.2    Schunemann, V.3    Kasche, V.4
  • 11
    • 0037013823 scopus 로고    scopus 로고
    • Reactivity of (Z)-4-arylidene-5(4H)-oxazolones: [4+2] Cycloaddition versus [4+3] cycloaddition/nucleophilic trapping
    • DOI 10.1016/S0040-4039(02)00744-X, PII S004040390200744X
    • A Avenoza JH Busto C Cativiela JM Peregrina 2002 Tetrahedron Lett 43 4167 10.1016/S0040-4039(02)00744-X 1:CAS:528:DC%2BD38Xjsl2hs7g%3D (Pubitemid 34603176)
    • (2002) Tetrahedron Letters , vol.43 , Issue.23 , pp. 4167-4170
    • Avenoza, A.1    Busto, J.H.2    Cativiela, C.3    Peregrina, J.M.4
  • 12
    • 0036124650 scopus 로고    scopus 로고
    • Novel hydrogels as supports for in vitro cell growth: Poly(ethylene glycol)- and gelatine-based (meth)acrylamidopeptide macromonomers
    • DOI 10.1016/S0142-9612(01)00343-X, PII S014296120100343X
    • J Zimmermann K Bittner B Stark R Mulhaupt 2002 Biomaterials 23 2127 10.1016/S0142-9612(01)00343-X 1:CAS:528:DC%2BD38XhvVWhs7c%3D (Pubitemid 34226572)
    • (2002) Biomaterials , vol.23 , Issue.10 , pp. 2127-2134
    • Zimmermann, J.1    Bittner, K.2    Stark, B.3    Mulhaupt, R.4
  • 13
    • 29744439251 scopus 로고    scopus 로고
    • Isolation, synthesis and photochemical properties of almazolone, a new indole alkaloid from a red alga of Senegal
    • DOI 10.1016/j.tet.2005.10.072, PII S0040402005019587
    • G Guella I N'Diaye M Fofana I Mancini 2006 Tetrahedron 62 1165 10.1016/j.tet.2005.10.072 1:CAS:528:DC%2BD28Xhs1eitA%3D%3D (Pubitemid 43031306)
    • (2006) Tetrahedron , vol.62 , Issue.6 , pp. 1165-1170
    • Guella, G.1    N'Diaye, I.2    Fofana, M.3    Mancini, I.4
  • 14
    • 0009518426 scopus 로고
    • 10.1039/qr9550900150 1:CAS:528:DyaG2MXmsVOrtA%3D%3D
    • EQ Baltazzi 1955 Rev Chem Soc 9 150 10.1039/qr9550900150 1:CAS:528:DyaG2MXmsVOrtA%3D%3D
    • (1955) Rev Chem Soc , vol.9 , pp. 150
    • Baltazzi, E.Q.1
  • 18
    • 61649088179 scopus 로고    scopus 로고
    • 10.1016/j.tet.2009.02.011 1:CAS:528:DC%2BD1MXjt1artrc%3D
    • PA Conway K Devine F Paradisi 2009 Tetrahedron 65 2935 10.1016/j.tet.2009.02.011 1:CAS:528:DC%2BD1MXjt1artrc%3D
    • (2009) Tetrahedron , vol.65 , pp. 2935
    • Conway, P.A.1    Devine, K.2    Paradisi, F.3
  • 22
    • 0032575183 scopus 로고    scopus 로고
    • In situ alcohol oxidation-Wittig reactions
    • DOI 10.1016/S0040-4039(98)00592-9, PII S0040403998005929
    • X Wei RJK Taylor 1998 Tetrahedron Lett 39 3815 10.1016/S0040-4039(98) 00592-9 1:CAS:528:DyaK1cXjtlamt7c%3D (Pubitemid 28222482)
    • (1998) Tetrahedron Letters , vol.39 , Issue.22 , pp. 3815-3818
    • Wei, X.1    Taylor, R.J.K.2
  • 24
    • 55749094501 scopus 로고    scopus 로고
    • 10.1016/j.matchemphys.2008.06.046 1:CAS:528:DC%2BD1cXhtlyht7jE
    • T Rajkumar GR Rao 2008 Mater Chem Phys 112 853 10.1016/j.matchemphys. 2008.06.046 1:CAS:528:DC%2BD1cXhtlyht7jE
    • (2008) Mater Chem Phys , vol.112 , pp. 853
    • Rajkumar, T.1    Rao, G.R.2
  • 27
    • 33751116080 scopus 로고    scopus 로고
    • Erlenmeyer synthesis for azlactones catalyzed by ytterbium(III) triflate under solvent-free conditions
    • DOI 10.1080/00397910600941521, PII T0514813X5M74073
    • C Yu B Zhou W Su Xu Zh 2006 Synth Commun 36 3447 10.1080/ 00397910600941521 1:CAS:528:DC%2BD2sXmslSmsQ%3D%3D (Pubitemid 44764433)
    • (2006) Synthetic Communications , vol.36 , Issue.22 , pp. 3447-3453
    • Yu, C.1    Zhou, B.2    Su, W.3    Xu, Z.4
  • 28
    • 0347627365 scopus 로고    scopus 로고
    • Calcium acetate catalyzed synthesis of 4-arylidene-2-phenyl-5(4H)- oxazolones under solvent-free conditions
    • DOI 10.1016/j.tetlet.2003.10.125
    • S Paul P Nanda R Gupta A Loupy 2004 Tetrahedron Lett 45 425 10.1016/j.tetlet.2003.10.125 1:CAS:528:DC%2BD3sXpslOjtrY%3D (Pubitemid 37542291)
    • (2004) Tetrahedron Letters , vol.45 , Issue.2 , pp. 425-427
    • Paul, S.1    Nanda, P.2    Gupta, R.3    Loupy, A.4
  • 32
    • 0346339564 scopus 로고    scopus 로고
    • Asymmetric transformation of chiral auxiliary-substituted N-acyl-α-dehydro(1-naphthyl)alanines into 3,4-dihydrobenzo[f]quinolinone derivatives via photoinduced electron transfer
    • DOI 10.1016/j.tet.2003.11.071
    • K Maekawa K Kubob T Igarashia T Sakurai 2004 Tetrahedron 60 1183 10.1016/j.tet.2003.11.071 1:CAS:528:DC%2BD2cXktVWqtQ%3D%3D (Pubitemid 38068381)
    • (2004) Tetrahedron , vol.60 , Issue.5 , pp. 1183-1189
    • Maekawa, K.1    Kubo, K.2    Igarashi, T.3    Sakurai, T.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.