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Volumn 55, Issue 12, 2002, Pages 1076-1080

Total synthesis of a-tetracyclic anti-tumor, UCE6

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; UCE 6; UNCLASSIFIED DRUG;

EID: 0036956433     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.7164/antibiotics.55.1076     Document Type: Letter
Times cited : (9)

References (9)
  • 1
    • 0030789769 scopus 로고    scopus 로고
    • UCE6, a new antitumor antibiotic with topoisomerase I-mediated DNA cleavage activity produced by actinomycetes: Producing organism, fermentation, isolation and biological activity
    • FUJII, N.; F. TANAKA, Y. YAMASHITA, T. ASHIZAWA, S. CHIBA & H. NAKANO: UCE6, a new antitumor antibiotic with topoisomerase I-mediated DNA cleavage activity produced by actinomycetes: producing organism, fermentation, isolation and biological activity. J. Antibiotics 50: 490-495, 1997
    • (1997) J. Antibiotics , vol.50 , pp. 490-495
    • Fujii, N.1    Tanaka, F.2    Yamashita, Y.3    Ashizawa, T.4    Chiba, S.5    Nakano, H.6
  • 2
    • 0027272448 scopus 로고
    • UCE6, a new antitumor antibiotic with topoisomerase I mediated DNA cleavage activity, from actinomycetes
    • FUJII, N.; Y. YAMASHITA, S. CHIBA, Y. UOSAKI, Y. SAITOH, Y. TUJI & H. NAKANO: UCE6, a new antitumor antibiotic with topoisomerase I mediated DNA cleavage activity, from actinomycetes. J. Antibiotics 46: 1173-1174, 1993
    • (1993) J. Antibiotics , vol.46 , pp. 1173-1174
    • Fujii, N.1    Yamashita, Y.2    Chiba, S.3    Uosaki, Y.4    Saitoh, Y.5    Tuji, Y.6    Nakano, H.7
  • 3
    • 0012570677 scopus 로고    scopus 로고
    • Total syntheses of useful bioactive compounds
    • TATSUTA, K.: Total syntheses of useful bioactive compounds. Adv. Synth. Catal. 343: 143-159, 2001
    • (2001) Adv. Synth. Catal. , vol.343 , pp. 143-159
    • Tatsuta, K.1
  • 5
    • 0000338285 scopus 로고
    • Diels-Alder reactions of 2-carbomethoxy-2-cyclohexen-1-one
    • Liu, H.-J.; T. K. NGOOI & E. N. C. BROWNE: Diels-Alder reactions of 2-carbomethoxy-2-cyclohexen-1-one. Can. J. Chem. 66: 3143-3152, 1988
    • (1988) Can. J. Chem. , vol.66 , pp. 3143-3152
    • Liu, H.-J.1    Ngooi, T.K.2    Browne, E.N.C.3
  • 6
    • 0034625897 scopus 로고    scopus 로고
    • A new method for the one-step synthesis of α,β-unsaturated carbonyl systems from saturated alcohols and carbonyl compounds
    • NICOLAOU, K. C.; Y.-L. ZHONG & P. S. BARAN: A new method for the one-step synthesis of α,β-unsaturated carbonyl systems from saturated alcohols and carbonyl compounds. J. Am. Chem. Soc. 122: 7596-7597, 2000
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 7596-7597
    • Nicolaou, K.C.1    Zhong, Y.-L.2    Baran, P.S.3
  • 7
    • 0000194961 scopus 로고
    • Enantio- and diastereoselective aldol reactions of achiral ethyl and methyl ketones with aldehydes: The use of enol diisopinocampheylborinates
    • PATERSON, I.; J. M. GOODMAN, M. A. LISTER, R. C. SCHUMANN, C. K. MCCLURE & R. D. NORCROSS: Enantio- and diastereoselective aldol reactions of achiral ethyl and methyl ketones with aldehydes: the use of enol diisopinocampheylborinates. Tetrahedron 46: 4663-4684, 1990
    • (1990) Tetrahedron , vol.46 , pp. 4663-4684
    • Paterson, I.1    Goodman, J.M.2    Lister, M.A.3    Schumann, R.C.4    Mcclure, C.K.5    Norcross, R.D.6
  • 8
    • 0032512595 scopus 로고    scopus 로고
    • Catalyzed enantioselective aldol additions of latent enolate equivalents
    • NELSON, S. G.: Catalyzed enantioselective aldol additions of latent enolate equivalents. Tetrahedron: Asymmetry 9: 357-389, 1998
    • (1998) Tetrahedron: Asymmetry , vol.9 , pp. 357-389
    • Nelson, S.G.1
  • 9
    • 85036706581 scopus 로고    scopus 로고
    • An authentic sample of natural UCE6 was kindly provided by Dr. Y. KANDA, Kyowa Hakko Kogyo Co., Ltd
    • An authentic sample of natural UCE6 was kindly provided by Dr. Y. KANDA, Kyowa Hakko Kogyo Co., Ltd.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.