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Volumn 50, Issue 7, 1997, Pages 598-613

1β-methyl-2-(5-substituted pyrrolidin-3-ylthio)carbapenems; 3. Synthesis and antibacterial activity of BO-2727 and its related compounds

Author keywords

[No Author keywords available]

Indexed keywords

DRUG DERIVATIVE; IMIPENEM; KIDNEY ENZYME; LENAPENEM; MEROPENEM;

EID: 0030856782     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.7164/antibiotics.50.598     Document Type: Article
Times cited : (21)

References (9)
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    • Synthetic carbapenem antibiotics I, 1β-methylcarbapenem
    • SHIH, D. H.; F. BAKER, L. CAMA & B. G. CHRISTENSEN: Synthetic carbapenem antibiotics I, 1β-methylcarbapenem. Heterocycles 21: 29-40, 1984
    • (1984) Heterocycles , vol.21 , pp. 29-40
    • Shih, D.H.1    Baker, F.2    Cama, L.3    Christensen, B.G.4
  • 3
    • 0030838163 scopus 로고    scopus 로고
    • 1β-methyl-2-(5-substituted pyrrolidin-3-ylthio)carbapenems; 2. Synthesis and antibacterial activity of 5-aminopropyl and 5-aminopropenyl derivatives
    • OHTAKE, N.; O. OKAMOTO, S. KATO, R. USHIJIMA, H. FUKATSU & S. NAKAGAWA: 1β-methyl-2-(5-substituted pyrrolidin-3-ylthio)carbapenems; 2. Synthesis and antibacterial activity of 5-aminopropyl and 5-aminopropenyl derivatives. J. Antibiotics 50: 586-597, 1997
    • (1997) J. Antibiotics , vol.50 , pp. 586-597
    • Ohtake, N.1    Okamoto, O.2    Kato, S.3    Ushijima, R.4    Fukatsu, H.5    Nakagawa, S.6
  • 4
    • 0025805827 scopus 로고
    • New methods and reagents in organic synthesis. 92. A stereoselective synthesis of tilivalline and its analogs
    • MORI, S.; T. OHNO, H. HARADA, T. AOYAMA & T. SHIOIRI: New methods and reagents in organic synthesis. 92. A stereoselective synthesis of tilivalline and its analogs. Terahedron 47: 5051-5079, 1991
    • (1991) Terahedron , vol.47 , pp. 5051-5079
    • Mori, S.1    Ohno, T.2    Harada, H.3    Aoyama, T.4    Shioiri, T.5
  • 5
    • 0001689925 scopus 로고
    • Stereoselective addition of lithioethyl acetate to Boc-L-prolinal. A conveinient chiral synthetic building block for the pyrrolizidine alkaloid ring system
    • HANSON, G. J.; J. S. BARAN &T. LINDBERG: Stereoselective addition of lithioethyl acetate to Boc-L-prolinal. A conveinient chiral synthetic building block for the pyrrolizidine alkaloid ring system.Terahedron Lett. 27: 3577-3580, 1986
    • (1986) Terahedron Lett. , vol.27 , pp. 3577-3580
    • Hanson, G.J.1    Baran, J.S.2    Lindberg, T.3
  • 6
    • 0021477495 scopus 로고
    • The preparation of N-protected amino alcohols and N-protected peptide alcohol by reduction of the corresponding esters with sodium borohydride. An improved procedure involving a slow addition of a small amount of methanol
    • SOAI, K.; H. OYAMADA & M. TAKASE: The preparation of N-protected amino alcohols and N-protected peptide alcohol by reduction of the corresponding esters with sodium borohydride. An improved procedure involving a slow addition of a small amount of methanol. Bull. Chem. Soc. Jpn. 57: 2327-2328, 1984
    • (1984) Bull. Chem. Soc. Jpn. , vol.57 , pp. 2327-2328
    • Soai, K.1    Oyamada, H.2    Takase, M.3
  • 7
    • 0030871084 scopus 로고    scopus 로고
    • 1β-methyl-2-(5-substituted pyrrolidin-3-ylthio)carbapenems; 1. Synthesis and antibacterial activity of BO-2502A and its related compounds
    • OHTAKE, N.; K. YAMABA, O. OKAMOTO, E. MANO, R. USHIJIMA & S. NAKAGAWA: 1β-methyl-2-(5-substituted pyrrolidin-3-ylthio)carbapenems; 1. Synthesis and antibacterial activity of BO-2502A and its related compounds. J. Antibiotics 50: 567-585, 1997
    • (1997) J. Antibiotics , vol.50 , pp. 567-585
    • Ohtake, N.1    Yamaba, K.2    Okamoto, O.3    Mano, E.4    Ushijima, R.5    Nakagawa, S.6
  • 9
    • 0029039624 scopus 로고
    • In vitro and in vivo antibacterial activities of BO-2727, a new carbapenem
    • ASAHI, Y.; S. MIYAZAKI & K. YMAGUCHI: In vitro and in vivo antibacterial activities of BO-2727, a new carbapenem. Antimicrob. Agents Chemother. 39: 1030-1037, 1995
    • (1995) Antimicrob. Agents Chemother. , vol.39 , pp. 1030-1037
    • Asahi, Y.1    Miyazaki, S.2    Ymaguchi, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.