메뉴 건너뛰기




Volumn 34, Issue 3, 2004, Pages 413-420

One Step Synthesis of Novel Antimicrobial 2-Hydroxy Diaryl Ethers Through Domestic Microwave Heating

Author keywords

Diaryl ether; Microwave and fatty acid synthesis

Indexed keywords

2 HYDROXY DIETHER; 4 CHLORO 2 (3 CHLOROPHENOXY)PHENOL; 4 CHLORO 2 (3,5 DICHLOROPHENOXY)PHENOL; 4 CHLORO 2 (5 CHLOROQUINOLIN 8 YLOXY)PHENOL; 4 CHLORO 2 (5,6,7,8 TETRAHYDRONAPHTHALEN 2 YLOXY)PHENOL; 4 CHLORO 2 (PYRAZOLO[3,4 D]PYRIMIDIN 4 YLOXY)PHENOL; 4 CHLORO 2 (QUINAZOLIN 4 YLOXY)PHENOL; ANTIINFECTIVE AGENT; UNCLASSIFIED DRUG;

EID: 1542346126     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1081/SCC-120027280     Document Type: Article
Times cited : (7)

References (14)
  • 1
    • 0028946308 scopus 로고
    • Use of pyridine as cocatalyst for the synthesis of 2-carboxy diphenyl ethers by Ullmanngoldberg condensation
    • Pellon, R.F.; Carrasco, R.; Milian, V.; Rodes, L. Use of pyridine as cocatalyst for the synthesis of 2-carboxy diphenyl ethers by Ullmanngoldberg condensation. Synth. Commun. 1995, 25 (7), 1077-1083.
    • (1995) Synth. Commun. , vol.25 , Issue.7 , pp. 1077-1083
    • Pellon, R.F.1    Carrasco, R.2    Milian, V.3    Rodes, L.4
  • 2
    • 0012876023 scopus 로고
    • Approaches to the synthesis of the vancomycin aglycones
    • Nagarajan, R., Ed.; Marcel Decker Inc.: New York
    • Evans, D.A.; DeVries, K.M. Approaches to the synthesis of the vancomycin aglycones. In Glycopeptide Antibiotics, Drugs and Pharmaceutical Sciences; Nagarajan, R., Ed.; Marcel Decker Inc.: New York, 1994, Vol. 63; 63-104.
    • (1994) Glycopeptide Antibiotics, Drugs and Pharmaceutical Sciences , vol.63 , pp. 63-104
    • Evans, D.A.1    DeVries, K.M.2
  • 3
    • 0037007703 scopus 로고    scopus 로고
    • Diaryl ether synthesis: Rate acceleration by 2,2,6,6-tetramethylheptane-3,5-dione
    • Buck, E.; Song, Z.J.; Tschaen, D.; Dormer, P.G.; Volante, R.P.; Reider, P.J. Diaryl ether synthesis: rate acceleration by 2,2,6,6-tetramethylheptane-3,5-dione. Ullmann Org. Lett. 2002, 4 (9), 1623-1626.
    • (2002) Ullmann Org. Lett. , vol.4 , Issue.9 , pp. 1623-1626
    • Buck, E.1    Song, Z.J.2    Tschaen, D.3    Dormer, P.G.4    Volante, R.P.5    Reider, P.J.6
  • 4
    • 84979085204 scopus 로고
    • Ueber eine neue darstellungsweise von phenylathersalicylsaure
    • Ullamann, F. Ueber eine neue darstellungsweise von phenylathersalicylsaure. Chem. Ber. 1904, 37, 853-854.
    • (1904) Chem. Ber. , vol.37 , pp. 853-854
    • Ullamann, F.1
  • 5
    • 0345329013 scopus 로고
    • Copper assisted nucleophilic substitution of aryl halogen
    • Lindley, J. Copper assisted nucleophilic substitution of aryl halogen. Tetrahedron 1984, 40 (9), 1433-1456.
    • (1984) Tetrahedron , vol.40 , Issue.9 , pp. 1433-1456
    • Lindley, J.1
  • 6
    • 0342757538 scopus 로고    scopus 로고
    • Recent advances in diaryl ether synthesis
    • Sawyer, J.S. Recent advances in diaryl ether synthesis. Tetrahedron 2000, 56 (29), 5045-5065.
    • (2000) Tetrahedron , vol.56 , Issue.29 , pp. 5045-5065
    • Sawyer, J.S.1
  • 7
    • 0034738131 scopus 로고    scopus 로고
    • Using intelligent/random library screening to design focused libraries for the optimization of homogeneous catalysts: Ullmann ether formation
    • Fagan, P.J.; Hauptman, E.; Shapiro, R.; Casalnuovo, A. Using intelligent/ random library screening to design focused libraries for the optimization of homogeneous catalysts: Ullmann ether formation. J. Am. Chem. Soc. 2000, 122 (21), 5043-5051.
    • (2000) J. Am. Chem. Soc. , vol.122 , Issue.21 , pp. 5043-5051
    • Fagan, P.J.1    Hauptman, E.2    Shapiro, R.3    Casalnuovo, A.4
  • 8
    • 0030700314 scopus 로고    scopus 로고
    • A general copper-catalyzed synthesis of diaryl ethers
    • Marcoux, J.F.; Doye, S.; Buchwald, S.L. A general copper-catalyzed synthesis of diaryl ethers. J. Am. Chem. Soc. 1997, 119 (43), 10539-10540.
    • (1997) J. Am. Chem. Soc. , vol.119 , Issue.43 , pp. 10539-10540
    • Marcoux, J.F.1    Doye, S.2    Buchwald, S.L.3
  • 9
    • 0033549049 scopus 로고    scopus 로고
    • Novel electron-rich bulky phosphine ligands facilitate the palladium-catalyzed preparation of diaryl ethers
    • Aranyos, A.; Old, D.W.; Kiyamori, A.; Wolfe, J.P.; Sadighi, J.P.; Buchwald, S.L. Novel electron-rich bulky phosphine ligands facilitate the palladium-catalyzed preparation of diaryl ethers. J. Am. Chem. Soc. 1999, 121 (18), 4369-4378.
    • (1999) J. Am. Chem. Soc. , vol.121 , Issue.18 , pp. 4369-4378
    • Aranyos, A.1    Old, D.W.2    Kiyamori, A.3    Wolfe, J.P.4    Sadighi, J.P.5    Buchwald, S.L.6
  • 10
    • 0030780953 scopus 로고    scopus 로고
    • Palladium catalyzed formation of diaryl ethers from aryl bromides. Electron poor phosphines enhance reaction yields
    • Mann, G.; Hartwig, J.F. Palladium catalyzed formation of diaryl ethers from aryl bromides. Electron poor phosphines enhance reaction yields. Tetrahedron Lett. 1997, 38 (46), 8005-8008.
    • (1997) Tetrahedron Lett. , vol.38 , Issue.46 , pp. 8005-8008
    • Mann, G.1    Hartwig, J.F.2
  • 11
    • 33947336698 scopus 로고
    • Solvent assisted Ullmann ether synthesis. Reaction of dihydric phenol
    • Williams, A.L.; Kinney, R.E.; Bridger, R.F. Solvent assisted Ullmann ether synthesis. Reaction of dihydric phenol. J. Org. Chem. 1967, 32 (8), 2501-2505.
    • (1967) J. Org. Chem. , vol.32 , Issue.8 , pp. 2501-2505
    • Williams, A.L.1    Kinney, R.E.2    Bridger, R.F.3
  • 12
    • 0000673247 scopus 로고
    • Ullmann condensation
    • Weingarten, H. Ullmann condensation. J. Org. Chem. 1964, 29 (1), 977-978.
    • (1964) J. Org. Chem. , vol.29 , Issue.1 , pp. 977-978
    • Weingarten, H.1
  • 13
    • 0032515066 scopus 로고    scopus 로고
    • Broad spectrum antimicrobial biocides target the FabI component of fatty acid synthesis
    • Heath, R.J.; Yu, Y.-T.; Shapiro, M.A.; Olson, E.; Rock, C.O. Broad spectrum antimicrobial biocides target the FabI component of fatty acid synthesis. J. Biol. Chem. 1998, 273 (46), 30316-30320.
    • (1998) J. Biol. Chem. , vol.273 , Issue.46 , pp. 30316-30320
    • Heath, R.J.1    Yu, Y.-T.2    Shapiro, M.A.3    Olson, E.4    Rock, C.O.5
  • 14
    • 0035126479 scopus 로고    scopus 로고
    • Triclosan offers protection against blood stages of malaria by inhibiting enuyl-ACP reductase of Plasmodium falciparum
    • Surolia, N.; Surolia, A. Triclosan offers protection against blood stages of malaria by inhibiting enuyl-ACP reductase of Plasmodium falciparum. Nature Med. 2001, 7 (2), 167-173.
    • (2001) Nature Med. , vol.7 , Issue.2 , pp. 167-173
    • Surolia, N.1    Surolia, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.