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Volumn 56, Issue 31, 2000, Pages 5621-5629

Generation of penems, carbapenems and aza analogs of cephems by the addition of heterocycles and other building blocks to azetinones

Author keywords

Azetinones; Carbapenems; Penems

Indexed keywords

CARBAPENEM DERIVATIVE; PENEM DERIVATIVE;

EID: 0034725745     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00411-7     Document Type: Article
Times cited : (11)

References (35)
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    • For recent reviews on β-lactam antibiotics, see: (a)
    • For recent reviews on β-lactam antibiotics, see: (a) Maiti, S. N.; Phillips, O. A.; Micetich, R. G.; Livermore, D. M. Curr. Med. Chem. 1998, 5, 441. (b) Berks, A. H. Tetrahedron 1996, 52, 331. (c) Southgate, R.; Branch, C.; Coulton, S.; Hunt, E. Recent Prog. Chem. Synth. Antibiot. Relat. Microb. Prod. 1993, 621.
    • (1998) Curr. Med. Chem. , vol.5 , pp. 441
    • Maiti, S.N.1    Phillips, O.A.2    Micetich, R.G.3    Livermore, D.M.4
  • 2
    • 0030028910 scopus 로고    scopus 로고
    • (b)
    • For recent reviews on β-lactam antibiotics, see: (a) Maiti, S. N.; Phillips, O. A.; Micetich, R. G.; Livermore, D. M. Curr. Med. Chem. 1998, 5, 441. (b) Berks, A. H. Tetrahedron 1996, 52, 331. (c) Southgate, R.; Branch, C.; Coulton, S.; Hunt, E. Recent Prog. Chem. Synth. Antibiot. Relat. Microb. Prod. 1993, 621.
    • (1996) Tetrahedron , vol.52 , pp. 331
    • Berks, A.H.1
  • 4
    • 84991428166 scopus 로고    scopus 로고
    • This azetidinone known as 'azetidon-Kaneka' is extensively used as a versatile building block for the syntheses of carbapenems and other β-lactam antibiotics. For synthetic routes to these compounds, see Ref. 1b
    • This azetidinone known as 'azetidon-Kaneka' is extensively used as a versatile building block for the syntheses of carbapenems and other β-lactam antibiotics. For synthetic routes to these compounds, see Ref. 1b.
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    • For reactions of enolate of diacyl ylides, see: (a)
    • For reactions of enolate of diacyl ylides, see: (a) Wasserman, H. H.; Lee, G. M. Tetrahedron Lett. 1994, 35, 9783. (b) Cooke, M. P., Jr. J. Org. Chem. 1982, 47, 4963. (c) Cooke, M. P., Jr.; Burman, D. L. J. Org. Chem. 1982, 47, 4955. (d) Taylor, J. D.; Wolf, J. F. J. Chem. Soc., Chem. Commun. 1972, 876.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 9783
    • Wasserman, H.H.1    Lee, G.M.2
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    • (b)
    • For reactions of enolate of diacyl ylides, see: (a) Wasserman, H. H.; Lee, G. M. Tetrahedron Lett. 1994, 35, 9783. (b) Cooke, M. P., Jr. J. Org. Chem. 1982, 47, 4963. (c) Cooke, M. P., Jr.; Burman, D. L. J. Org. Chem. 1982, 47, 4955. (d) Taylor, J. D.; Wolf, J. F. J. Chem. Soc., Chem. Commun. 1972, 876.
    • (1982) J. Org. Chem. , vol.47 , pp. 4963
    • Cooke, M.P.1
  • 18
    • 0000749788 scopus 로고
    • (c)
    • For reactions of enolate of diacyl ylides, see: (a) Wasserman, H. H.; Lee, G. M. Tetrahedron Lett. 1994, 35, 9783. (b) Cooke, M. P., Jr. J. Org. Chem. 1982, 47, 4963. (c) Cooke, M. P., Jr.; Burman, D. L. J. Org. Chem. 1982, 47, 4955. (d) Taylor, J. D.; Wolf, J. F. J. Chem. Soc., Chem. Commun. 1972, 876.
    • (1982) J. Org. Chem. , vol.47 , pp. 4955
    • Cooke, M.P.1    Burman, D.L.2
  • 19
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    • (d)
    • For reactions of enolate of diacyl ylides, see: (a) Wasserman, H. H.; Lee, G. M. Tetrahedron Lett. 1994, 35, 9783. (b) Cooke, M. P., Jr. J. Org. Chem. 1982, 47, 4963. (c) Cooke, M. P., Jr.; Burman, D. L. J. Org. Chem. 1982, 47, 4955. (d) Taylor, J. D.; Wolf, J. F. J. Chem. Soc., Chem. Commun. 1972, 876.
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    • Taylor, J.D.1    Wolf, J.F.2
  • 25
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    • Product 30 is related to the tricyclic hydroxy cephem derivative 33 reported to have antibiotic activity
    • Product 30 is related to the tricyclic hydroxy cephem derivative 33 reported to have antibiotic activity. Sheehan, J. C.; Dalzell, H. C.; Greenwood, J. M.; Ponzi, D. R. J. Org. Chem. 1974, 39, 277.
    • (1974) J. Org. Chem. , vol.39 , pp. 277
    • Sheehan, J.C.1    Dalzell, H.C.2    Greenwood, J.M.3    Ponzi, D.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.