메뉴 건너뛰기




Volumn 40, Issue 22, 2010, Pages 3281-3289

Aqueous synthesis of N-phenyl/alkyl-2-quinolinone-3-carboxylic acids from coumarin-3-carboxylic acids

Author keywords

Coumarin 3 carboxylic acid; N phenyl=alkyl 2 quinolinones; one pot

Indexed keywords

AMINE; CARBOXYLIC ACID DERIVATIVE; COUMARIN DERIVATIVE; QUINOLINE DERIVATIVE;

EID: 77958071337     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910903399690     Document Type: Article
Times cited : (13)

References (16)
  • 1
    • 85064407458 scopus 로고
    • Total synthesis of (±)-virantmycin and determination of its stereochemistry
    • Morimoto, Y.; Matusuda, F.; Shirahama, H. Total synthesis of (±)-virantmycin and determination of its stereochemistry. Synlett 1991, 202-203.
    • (1991) Synlett , pp. 202-203
    • Morimoto, Y.1    Matusuda, F.2    Shirahama, H.3
  • 2
    • 0014750166 scopus 로고
    • Antiprotozoal 4-aryloxy-2-aminoquinolines and related compounds
    • Markees, D. G.; Dewey, V. C.; Kidder, G. W. Antiprotozoal 4-aryloxy-2-aminoquinolines and related compounds. J. Med. Chem. 1970, 13, 324.
    • (1970) J. Med. Chem. , vol.13 , pp. 324
    • Markees, D.G.1    Dewey, V.C.2    Kidder, G.W.3
  • 3
    • 0023936336 scopus 로고    scopus 로고
    • 2,4-Diamino-6,7-dimethoxyquinoline derivatives as a-1-adrenocept-or antagonists and antihypertensive agents
    • Campbell, S. F.; Hardstone, J. D.; Palmer, M. J. 2,4-Diamino-6,7- dimethoxyquinoline derivatives as a-1-adrenocept-or antagonists and antihypertensive agents. J. Med. Chem. 1998, 31, 1031.
    • (1998) J. Med. Chem. , vol.31 , pp. 1031
    • Campbell, S.F.1    Hardstone, J.D.2    Palmer, M.J.3
  • 4
    • 0033693276 scopus 로고    scopus 로고
    • Inhibition of autoimmune disease by the immunomodulator linomide correlates with the ability to activate macrophages
    • Dahlen, E.; Andersson, M.; Dawe, K.; Tellander, A. C.; Brunmark, C.; Bjork, A.; Hedlung, G. Inhibition of autoimmune disease by the immunomodulator linomide correlates with the ability to activate macrophages. Autoimmunity 2000, 32, 198-211
    • (2000) Autoimmunity , vol.32 , pp. 198-211
    • Dahlen, E.1    Andersson, M.2    Dawe, K.3    Tellander, A.C.4    Brunmark, C.5    Bjork, A.6    Hedlung, G.7
  • 8
    • 0038739204 scopus 로고    scopus 로고
    • An efficient route from coumarins to highly functionalized N-phenyl-2-quinolinones via Buchwald-Hartwig amination
    • WO 91-US6251, 1995
    • Afonso A.,Weinstein J.,Gentles M. J. WO 91-US6251, 1995; An efficient route from coumarins to highly functionalized N-phenyl-2-quinolinones via Buchwald-Hartwig amination. Tetrahedron Lett., 2003, 44, 4207-4211.
    • (2003) Tetrahedron Lett. , vol.44 , pp. 4207-4211
    • Afonso, A.1    Weinstein, J.2    Gentles, M.J.3
  • 9
    • 84986518955 scopus 로고
    • Preparation and proton spectra of 1-ary1-1,2-dihydro-2-quinolones
    • Wawzonek, S.; VanTruong, T. Preparation and proton spectra of 1-ary1-1,2-dihydro-2-quinolones. J. Heterocycl. Chem. 1988, 25, 381-382.
    • (1988) J. Heterocycl. Chem. , vol.25 , pp. 381-382
    • Wawzonek, S.1    Vantruong, T.2
  • 10
    • 0033615795 scopus 로고    scopus 로고
    • N-Aryl heterocycles via coupling reactions with arylboronic acids
    • Mederski, W. W. K. R.; Lefort, M.; Germann, M.; Kux, D. N-Aryl heterocycles via coupling reactions with arylboronic acids. Tetrahedron 1999, 55, 12757-12770.
    • (1999) Tetrahedron , vol.55 , pp. 12757-12770
    • Mederski, W.W.K.R.1    Lefort, M.2    Germann, M.3    Kux, D.4
  • 11
    • 33748533856 scopus 로고    scopus 로고
    • 1,2-Dihydroquinolin-2-one(carbos-tyril) anions as bidentate nucleophiles in their reactions with aryllead triacetates: Synthesis of 1-aryl-and 3-aryl-tetrahydroquinoline-2 5,8-triones
    • Lopez-Alvarado, P.; Avendano, C.; Menendez, J. C. 1,2-Dihydroquinolin-2- one(carbos-tyril) anions as bidentate nucleophiles in their reactions with aryllead triacetates: Synthesis of 1-aryl-and 3-aryl-tetrahydroquinoline-2,5,8- triones. J. Chem. Soc., Perkin Trans. 1 1997, 229-233.
    • (1997) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 229-233
    • Lopez-Alvarado, P.1    Avendano, C.2    Menendez, J.C.3
  • 12
    • 0033032933 scopus 로고    scopus 로고
    • Reaction of aminobenzimidazoles with 4-hydroxy-6-methyl-2-pyrone and 4-hydroxy-coumarin
    • El Kihel, A.; Benchidmi, M.; Essassi, E. M.; Basudha, P.; Danion-Bougot, R. Reaction of aminobenzimidazoles with 4-hydroxy-6-methyl-2-pyrone and 4-hydroxy-coumarin. Synth. Commun. 1999, 29, 2435-2445.
    • (1999) Synth. Commun. , vol.29 , pp. 2435-2445
    • El Kihel, A.1    Benchidmi, M.2    Essassi, E.M.3    Basudha, P.4    Danion-Bougot, R.5
  • 13
    • 0344996003 scopus 로고
    • Reaction of dehydroacetic acid with ammonia
    • Wang, C. S.; Easterly, J. P.; Skelly, N. E. Reaction of dehydroacetic acid with ammonia. Tetrahedron 1971, 27, 2581.
    • (1971) Tetrahedron , vol.27 , pp. 2581
    • Wang, C.S.1    Easterly, J.P.2    Skelly, N.E.3
  • 14
  • 15
    • 0037204923 scopus 로고    scopus 로고
    • 3-catalyzed domino reaction of aromatic amines with cyclic enol ethers in water: A highly efficient synthesis of new 1, 2, 3,4-tetrahydroquinoline derivatives
    • 3-catalyzed domino reaction of aromatic amines with cyclic enol ethers in water: A highly efficient synthesis of new 1,2,3,4-tetrahydroquinoline derivatives. J. Org. Chem. 2002, 67, 3969-3971.
    • (2002) J. Org. Chem. , vol.67 , pp. 3969-3971
    • Zhang, J.1    Li, C.-J.2
  • 16
    • 57449083494 scopus 로고    scopus 로고
    • Synthesis of 1-(2-methyl-1, 2, 3,4-tetrahydroquinolin-4-yl)pyrrolidin-2- ones from anilines and N-vinyl pyrrolidin-2-one through imino Diels-Alder reaction using 4-nitro phthalic acid as catalyst
    • Srinivasa, A.; Mahadevan, K. M.; Hulikal, V. Synthesis of 1-(2-methyl-1,2,3,4-tetrahydroquinolin-4-yl)pyrrolidin-2-ones from anilines and N-vinyl pyrrolidin-2-one through imino Diels-Alder reaction using 4-nitro phthalic acid as catalyst. Synth. Commun. 2009, 39, 93.
    • (2009) Synth. Commun. , vol.39 , pp. 93
    • Srinivasa, A.1    Mahadevan, K.M.2    Hulikal, V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.