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Volumn 50, Issue 7, 1997, Pages 586-597

1β-methyl-2-(5-substituted pyrrolidin-3-ylthio)carbapenems; 2. Synthesis and antibacterial activity of 5-aminopropyl and 5-aminopropenyl pyrrolidine derivatives

Author keywords

[No Author keywords available]

Indexed keywords

BO 2502A; CARBAPENEM DERIVATIVE; KIDNEY ENZYME; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0030838163     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.7164/antibiotics.50.586     Document Type: Article
Times cited : (7)

References (9)
  • 1
    • 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.; O. OKAMOTO, E. MANO, K. YAMADA, 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    Okamoto, O.2    Mano, E.3    Yamada, K.4    Ushijima, R.5    Nakagawa, S.6
  • 2
    • 33646066450 scopus 로고
    • Direct synthesis of Z-unsaturated esters. A useful modification of the Horner-Emmons olefination
    • STILL, W. C. & C. GENNARI: Direct synthesis of Z-unsaturated esters. A useful modification of the Horner-Emmons olefination. Tetrahedron Lett. 24: 4405-4408, 1983
    • (1983) Tetrahedron Lett. , vol.24 , pp. 4405-4408
    • Still, W.C.1    Gennari, C.2
  • 4
    • 33845470050 scopus 로고
    • Ate complex from diisobutyl-aluminum hydride and n-butyllithium as a powerful and selective reducing agent for the reduction of selected organic compounds containing various functional groups
    • KIM, S. & K. H. AHN: Ate complex from diisobutyl-aluminum hydride and n-butyllithium as a powerful and selective reducing agent for the reduction of selected organic compounds containing various functional groups. J. Org. Chem. 49: 1717-1724, 1984
    • (1984) J. Org. Chem. , vol.49 , pp. 1717-1724
    • Kim, S.1    Ahn, K.H.2
  • 5
    • 45249127652 scopus 로고
    • Trialkylsilanes as scavenger for the trifluoroacetic acid deblocking of protecting in peptide synthesis
    • PEARSON, D. A.; M. BLANCHETTE, M. L. BAKER & C. A. GUINDON: Trialkylsilanes as scavenger for the trifluoroacetic acid deblocking of protecting in peptide synthesis. Tetrahedron Lett. 30: 2379-2742, 1989
    • (1989) Tetrahedron Lett. , vol.30 , pp. 2379-2742
    • Pearson, D.A.1    Blanchette, M.2    Baker, M.L.3    Guindon, C.A.4
  • 6
    • 0025329413 scopus 로고
    • Synthesis of chiral α-acetylenic cyclic amines from α-amino acids: Applications to differentially constrained oxotremorine analogues as muscarine agents
    • CHUNG, J. Y. L. & J. T. WASICAK: Synthesis of chiral α-acetylenic cyclic amines from α-amino acids: Applications to differentially constrained oxotremorine analogues as muscarine agents. Tetrahedron Lett. 28: 3957-3960, 1989
    • (1989) Tetrahedron Lett. , vol.28 , pp. 3957-3960
    • Chung, J.Y.L.1    Wasicak, J.T.2
  • 7
    • 0023856378 scopus 로고
    • An expeditious synthesis of a 1β-methylcarbapenem key intermediate
    • DEZIEL, R. & M. ENDO: An expeditious synthesis of a 1β-methylcarbapenem key intermediate. Tetrahedron Lett. 29: 61-64, 1988
    • (1988) Tetrahedron Lett. , vol.29 , pp. 61-64
    • Deziel, R.1    Endo, M.2
  • 8
    • 0002662579 scopus 로고
    • Synthetic carbapencm antibiotics I, 1β-methyl carbapenem
    • SHIH, D. H.; F. BAKER, L. CAMA & B. G. CHRISTENSEN: Synthetic carbapencm antibiotics I, 1β-methyl carbapenem. 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
  • 9
    • 33845282500 scopus 로고
    • Selective cleavage of the allyl and allyloxycarbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesis
    • DANGELS, O.; F. GUIBE & G. BALANBOIN, S. LAVIELLE & A. MARQUET: Selective cleavage of the allyl and allyloxycarbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application to the selective protection-deprotection of amino acid derivatives and in peptide synthesis. J. Org. Chem. 52: 4984-4993, 1987
    • (1987) J. Org. Chem. , vol.52 , pp. 4984-4993
    • Dangels, O.1    Guibe, F.2    Balanboin, G.3    Lavielle, S.4    Marquet, A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.