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Volumn 9, Issue 10, 1999, Pages 1347-1350

A highly stereoselective synthesis of plaunotol and its thiourea derivatives as potent antibacterial agents against Helicobacter pylori

Author keywords

[No Author keywords available]

Indexed keywords

PLAUNOTOL; THIOUREA DERIVATIVE;

EID: 0033577761     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(99)00203-6     Document Type: Article
Times cited : (26)

References (28)
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    • J. R. Warren, Lancet, 1983, i, 1273; B. J. Marshall, Lancet, 1983, i, 1273.
    • (1983) Lancet , vol.1 , pp. 1273
    • Marshall, B.J.1
  • 3
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    • B. J. Marshall, J. A. Armstrong, D. B. McGechie and R. J. Glancy, Med. J. Aust., 1985, 142, 436; C. A. M. McNulty, J. C. Gearty, B. Crump, M. Davis, I. A. Donovan, V. Melikian, D. M. Lister and R. Wise, Br. Med. J., 1986, 293, 645; A. Morris and G. Nicholson, Am. J. Gastroenterol., 1987, 82, 192.
    • (1985) Med. J. Aust. , vol.142 , pp. 436
    • Marshall, B.J.1    Armstrong, J.A.2    McGechie, D.B.3    Glancy, R.J.4
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    • B. J. Marshall, J. A. Armstrong, D. B. McGechie and R. J. Glancy, Med. J. Aust., 1985, 142, 436; C. A. M. McNulty, J. C. Gearty, B. Crump, M. Davis, I. A. Donovan, V. Melikian, D. M. Lister and R. Wise, Br. Med. J., 1986, 293, 645; A. Morris and G. Nicholson, Am. J. Gastroenterol., 1987, 82, 192.
    • (1987) Am. J. Gastroenterol. , vol.82 , pp. 192
    • Morris, A.1    Nicholson, G.2
  • 8
    • 0028774376 scopus 로고
    • R. P. H. Logan, Lancet, 1994, 344, 1078; International Agency for Research on Cancer, IARC Monogr. Eval. Carcing. Risks Hum., 1994, 61, 177.
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    • Logan, R.P.H.1
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    • R. P. H. Logan, Lancet, 1994, 344, 1078; International Agency for Research on Cancer, IARC Monogr. Eval. Carcing. Risks Hum., 1994, 61, 177.
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  • 23
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    • Synthesized by the same route as ethyldiethoxy acetoacetate, see T. B. Johnson and L. H. Cretcher, Jr., J. Am. Chem. Soc., 1915, 37, 2144; T. B. Johnson and L. A. Mikeska, J. Am. Chem. Soc., 1919, 41, 810.
    • (1915) J. Am. Chem. Soc. , vol.37 , pp. 2144
    • Johnson, T.B.1    Cretcher L.H., Jr.2
  • 24
    • 0000875826 scopus 로고
    • Synthesized by the same route as ethyldiethoxy acetoacetate, see T. B. Johnson and L. H. Cretcher, Jr., J. Am. Chem. Soc., 1915, 37, 2144; T. B. Johnson and L. A. Mikeska, J. Am. Chem. Soc., 1919, 41, 810.
    • (1919) J. Am. Chem. Soc. , vol.41 , pp. 810
    • Johnson, T.B.1    Mikeska, L.A.2
  • 25
    • 0013477009 scopus 로고    scopus 로고
    • The detailed study on this Wittig reaction will be described elsewhere
    • The detailed study on this Wittig reaction will be described elsewhere.
  • 27
    • 0013511061 scopus 로고    scopus 로고
    • 4 and DIBAL-H) caused partial reduction of imido carbonyls
    • 4 and DIBAL-H) caused partial reduction of imido carbonyls.
  • 28
    • 0013542653 scopus 로고    scopus 로고
    • For acetic acid-induced gastric ulcer in nude mice which were infected with H. pylori, 2a reduced the ulcer size (100mg/kg/day, 10 days). The detailed study on in vivo will be described elsewhere
    • For acetic acid-induced gastric ulcer in nude mice which were infected with H. pylori, 2a reduced the ulcer size (100mg/kg/day, 10 days). The detailed study on in vivo will be described elsewhere.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.