699-approximation algorithm for Max-Bisection - download pdf or read online

By Ye Y.

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R. Carle: (-)-a-Bisabolol 10. , Zaoral, M . Chem. Commun. , Dtsch. Apoth. Ztg. , Perfum. Ess. , Planta Med. , J. Org. Chem. , Z. Naturforsch. , Dtsch. Apoth. Ztg. , Hammerschmidt, F. , Planta Med. , Planta Med. 56 (1990) 456-460 (Adulteration, Isotope Ratio Mass Spectrometry) R. Carle: (-)-a-Bisabolol This Page Intentionally Left Blank Bryoflavone H. D. Zinsrneister, S. Anhut, R. Mues 1. Name of Compound Common name Bryoflavone [l] Synonyms Systematic name 6-[5-(5,7-Dihydroxy-4-oxo-4H-l-benzopyran-3-yl)-2,3-dihydroxyphenyl]2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-l-benzopyran-4-one Substance Subgroup Flavonoid Biflavonoid CAS registry number and other numbers [111200-22-71 2.

For structure elucidation only NMR spectroscopic techniques were used, since they allow a subsequent recovery. 10. , Mues, R. and Zinsmeister, H. D. : Bryoflavone and Heterobryoflavone, l b o New Isoflavone- Flavone Dimers from Bryum capillare. Z. Naturforsch. 42c, 1987, pp 863-7 (name, '-'C-NMR) [2] Geiger, H. : Biflavonoids. B. ), Chapman and Hall, London, 1988 (name, occurrence) [3] Chari, V. -C. -M. : I3C-NMR Spectroscopy of Biflavonoids. Phytochemistry 16, 1977, pp. R. M. : Carbon-13 NMR Spectroscopy of Flavonoids.

M. : I3C-NMR Spectroscopy of Biflavonoids. Phytochemistry 16, 1977, pp. R. M. : Carbon-13 NMR Spectroscopy of Flavonoids. In 'The Flavonoids', Harborne, J. B. and Mabry, T. J. ), Chapman and Hall London, 1982 (13C-NMR) [ 5 ] Mabry, T. , Markham, K. R. and Thomas, M. : The Systematic Identification of Flavonoids. Springer Verlag, 1970 (UVspectroscopy) H. D. Zinsmeister, S. Anhut, R. Mues: Bryoflavone Camphene 0. Vostrowsky 1. 2] heptane Substance Subgroup Terpene Monoterpene hydrocarbon CAS registry number and other numbers [79-92-51; (+): [5794-03-61; (-): [5794-04-71 Merck Index 10, 1708; Merck Index - 1736 n, RTECS EX1055000 BRN 1903765 (+): BRN 2323386 (-): BRN 2204256 2.

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699-approximation algorithm for Max-Bisection by Ye Y.


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