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Quantum Chemical Research of Quercetin, Myricetin, their Bromo- and Sulpho Derivatives

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Biodiversity

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Abstract

Structural diversity of flavonoids due to the rate of heterocyclic ring reduction, aromatic rings hydroxylation (A and B) and their wide presence in nature creates presuppositions for scientific application of these compounds for correction of more than 40 types of biochemical processes in living organisms1.

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References

  1. P.J. Macander Plant Flavonoids in Biology and Medicine. New York, 1986, p. 489–792.

    Google Scholar 

  2. F.E.жycyлoba, M.C. Epжahoba, K. Q. Paxhmob, C.M. Bepmehhes, O npomueoonyxoneeoü axmuehocmu npupodxbex otccuфnaeohoe u ux npupodxbex. Bcecohohbih Chmnosnym no фehonbhbim coethhemrm, Tallnih, 1987, pp.42–43

    Google Scholar 

  3. S.R. Husalne, J. Cillard, P. Cillard, Phytochem, 1987, vol. 26, N 9, P. 2489–2491

    Article  Google Scholar 

  4. Pacthtenbxble nexapetsexxble cpeacrsa. pot pert. H.N. Makccidythhon, Kies: 3Aoposbe, 1985, p. 99–101

    Google Scholar 

  5. J. Pincemall, Deby., Lion, Proc. 7th Hunng. Bioflavanoid Symp. Budapest, 1986, p. 423–436.

    Google Scholar 

  6. F.E.жycynosa, A.A. Hammon, M.C. Epxcaiosa, XNC 1995, No.4, p. 709–711

    Google Scholar 

  7. J.J.P. Stewart, J. Comp. Chem., 1989, 10, 221.

    Article  CAS  Google Scholar 

  8. B.H. BeteHees, J.B. Fypesm, B.H. Koxtpaybes, B.A. Metsetes, E.N. фpaxlceshx Dnepzuu paspbiea xumuvecxux cestseū. llomeytyuaabt uonusatyuu u cpodcmeo K snexmpoHy. Cnpasohhhx. AH CCCP, M., 1962, 216 c.

    Google Scholar 

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Author information

Authors and Affiliations

  1. Department of Chemistry, al-Farabi Kazakh National University, 95a Karasay-Batyr St., Almaty, Kazakhstan

    Galiya Zhusupova & V. Gapdrakipov

Authors
  1. Galiya Zhusupova
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  2. V. Gapdrakipov
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Editor information

Editors and Affiliations

  1. Gazi University, Ankara, Turkey

    Bilge Åžener

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© 2002 Springer Science+Business Media New York

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Zhusupova, G., Gapdrakipov, V. (2002). Quantum Chemical Research of Quercetin, Myricetin, their Bromo- and Sulpho Derivatives. In: Åžener, B. (eds) Biodiversity. Springer, Boston, MA. https://doi.org/10.1007/978-1-4419-9242-0_53

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  • DOI: https://doi.org/10.1007/978-1-4419-9242-0_53

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4613-4855-9

  • Online ISBN: 978-1-4419-9242-0

  • eBook Packages: Springer Book Archive

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