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Volumn 50, Issue 9, 1997, Pages 765-769

Selective deoxygenation and O-methylation of benanomicin A: Synthesis of 9-Deoxy-, 9-O-Methyl- and 14-O-Methylbenanomicin A

Author keywords

[No Author keywords available]

Indexed keywords

BENANOMICIN A; DRUG DERIVATIVE;

EID: 0030842322     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.7164/antibiotics.50.765     Document Type: Article
Times cited : (3)

References (11)
  • 2
    • 15144349192 scopus 로고
    • Identification of strain MH193-16F4, a benanomicin-producing Actinomycete, to Actinomadura spadix
    • KINOSHITA, N.; M. OKADA & M. HAMADA: Identification of strain MH193-16F4, a benanomicin-producing Actinomycete, to Actinomadura spadix. Actinomycetologica 8: 71-78, 1994
    • (1994) Actinomycetologica , vol.8 , pp. 71-78
    • Kinoshita, N.1    Okada, M.2    Hamada, M.3
  • 4
    • 0026592073 scopus 로고
    • Amino acid analogs of benanomicin A through desalaninebenanomicin A
    • IKEDA, D.; T. NISHIZUKA, S.-P. HUANG, S. KONDO & T. TAKEUCHI: Amino acid analogs of benanomicin A through desalaninebenanomicin A. J. Antibiotics 45: 1645-1652, 1992
    • (1992) J. Antibiotics , vol.45 , pp. 1645-1652
    • Ikeda, D.1    Nishizuka, T.2    Huang, S.-P.3    Kondo, S.4    Takeuchi, T.5
  • 6
    • 0001642236 scopus 로고
    • Palladium catalyzed triethylammonium formate reduction of aryl triflates. A selective method for the deoxygenation of phenols
    • CACCHI, S.; P. G. CIATTINI, E. MORERA & G. ORTAR: Palladium catalyzed triethylammonium formate reduction of aryl triflates. A selective method for the deoxygenation of phenols. Tetrahedron Lett. 27: 5541-5544, 1986
    • (1986) Tetrahedron Lett. , vol.27 , pp. 5541-5544
    • Cacchi, S.1    Ciattini, P.G.2    Morera, E.3    Ortar, G.4
  • 7
    • 0001033508 scopus 로고
    • Metal-assisted reactions. 13. Rapid, selective reductive cleavage of phenolic hydroxyl groups by catalytic transfer methods
    • and references cited therein
    • HUSSEY, B. J.; R. A. JOHNSTONE & I. D. ENTWISTLE: Metal-assisted reactions. 13. Rapid, selective reductive cleavage of phenolic hydroxyl groups by catalytic transfer methods. Tetrahedron 38: 3775-3781, 1982 and references cited therein
    • (1982) Tetrahedron , vol.38 , pp. 3775-3781
    • Hussey, B.J.1    Johnstone, R.A.2    Entwistle, I.D.3
  • 8
    • 0344218333 scopus 로고
    • Facile deoxygenation of phenols and enols using sodium borohydride-nickel chloride
    • WANG, F.; K. CHIBA & M. TADA: Facile deoxygenation of phenols and enols using sodium borohydride-nickel chloride. J. Chem. Soc. Perkin Trans. I 1992: 1897-1900
    • (1992) J. Chem. Soc. Perkin Trans. I , pp. 1897-1900
    • Wang, F.1    Chiba, K.2    Tada, M.3
  • 10
    • 0027476307 scopus 로고
    • Studies on the mode of antifungal action of pradimicin antibiotics. I. Lectin-mimic binding of BMY-28864 to yeast mannan in the presence of calcium
    • UEKI, T.; K. NUMATA, Y. SAWADA, T. NAKAJIMA, Y. FUKAGAWA & T. OKI: Studies on the mode of antifungal action of pradimicin antibiotics. I. Lectin-mimic binding of BMY-28864 to yeast mannan in the presence of calcium. J. Antibiotics 46: 149-161, 1993
    • (1993) J. Antibiotics , vol.46 , pp. 149-161
    • Ueki, T.1    Numata, K.2    Sawada, Y.3    Nakajima, T.4    Fukagawa, Y.5    Oki, T.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.