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Volumn 60, Issue 38, 2004, Pages 8547-8552

The absolute configuration of peroxisomicines A1 and A2

Author keywords

Chiral displacement reagent; Circular dichroism; Degradation; Dihydroxyanthracenones; Peroxisomicine

Indexed keywords

ANTINEOPLASTIC AGENT; DNA TOPOISOMERASE (ATP HYDROLYSING); KARWINSKIA EXTRACT; PEROXISOMICINE A1; PEROXISOMICINE A2; PLANT EXTRACT; UNCLASSIFIED DRUG;

EID: 4444253546     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.06.123     Document Type: Article
Times cited : (10)

References (25)
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    • Elsevier: Amsterdam
    • Piñeyro-López, A.; Waksman, N.; Studies in Natural Products Chemistry: The Anthracenones of Karwinskia genus. Chemistry, Structure and Biological Activity, Vol. 23; Elsevier: Amsterdam, 2000 pp 555-606.
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  • 9
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    • note
    • Strictly speaking, biarylic bis-preanthraquinones like 1a and 1b should be addressed as 'dehydro-dimers'; for reasons of simplicity, the term 'dimer' (and also 'monomer') will, however, be used throughout this paper.
  • 11
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    • W. Herz H. Grisebach G.W. Kirby C. Tamm Springer Wien
    • For similar compounds isolated from Cortinarius species, see: M. Gill, and W. Steglich W. Herz H. Grisebach G.W. Kirby C. Tamm Progress in the Chemistry of Organic Natural Products Vol. 51 1987 Springer Wien 125 174
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  • 14
    • 0001058577 scopus 로고
    • G. Helmchen R.W. Hoffmann J. Mulzer E. Schaumann Thieme Stuttgart
    • For the now recommended M/P denotation for axial chirality, see: (a) G. Helmchen G. Helmchen R.W. Hoffmann J. Mulzer E. Schaumann Methods of Organic Chemistry (Houben Weyl) Vol. E21a 1995 Thieme Stuttgart 11 13
    • (1995) Methods of Organic Chemistry (Houben Weyl) , vol.21 , pp. 11-13
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    • Bringmann1    Busemann, S.G.2
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    • Department of Chemistry and Biochemistry, University of Colorado: Boulder, USA; modified by Fleischhauer, J.; Schleker, W.; Kramer, B. Ported to Linux by Gulden, K.-P.
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    • Program Package BDZDO/MCDSPD
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.