Skip to main content
Log in

Study of the catechins and proanthocyanidins ofQuercus robur

  • Published:
Chemistry of Natural Compounds Aims and scope

Abstract

More than 20 compounds have been isolated from the bark ofQuercus robur. Monomers: (−)-epicatechin, (−)-epicatechin gallate, (+)-catechin, (+)-catechin gallate, (+)-gallocatechin, (−)-epigallocatechin, and (−)-epigallocatechin gallate; dimeric proanthocyanidins: (+)-catechin-(4α-8)-(+)-catechin, 3-O-galloyl-(+)-catechin-(4α-8)-3-O-galloyl-(+)-catechin, 3-O-galloyl-(+)-gallocatechin-(4β-8)-(+)-gallocatechin, (−)-epicatechin-(4β-8)-3-O-galloyl-(−)-epigallocatechin gallate, 3-O-galloyl-(−)-epicatechin-(4β-8)-3-O-galloyl-(−)-epigallocatechin, 3-O-galloyl-(−)-epigallocatechin-(4β-8)-(+)-catechin; and oligomeric proanthocyanidins: D14-D19.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. D. N. Enukidze and I. I. Maniava, Soobshch. Akad. Nauk GSSR,66, 101 (1972).

    Google Scholar 

  2. Byung-Zun Ahn, Arch. Pharm.,306, 617 (1973).

    Google Scholar 

  3. Byung-Zun Ahn, Arch. Pharm.,306, 338 (1973).

    Google Scholar 

  4. Byung-Zun Ahn, Arch. Pharm.,307, 186 (1974).

    Google Scholar 

  5. D., Sun, H. Wong, and I. Y. Foo, Phytochemistry,26, 1825 (1987).

    Google Scholar 

  6. K. Ishimaru, G.-I. Nonaka, and I. Nishioka, Phytochemistry,26, 1170 (1987).

    Google Scholar 

  7. A. Malik, Z. A. Kuliev, U. A. Akhmedov, A. D. Vdovin, and N. D. Abdullaev, Khim. Prir. Soedin., 221 (1997).

  8. A. Malik, Z. A. Kuliev, U. A. Akhmedov, A. D. Vdovin, and N. D. Abdullaev, Khim. Prir. Soedin. 232 (1997).

  9. A. D. Vdovin, Z. A. Kuliev, and N. D. Abdullaev, Khim. Prir. Soedin., 16 (1997).

  10. A. D. Vdovin, Z. A. Kuliev, and N. D. Abdullaev, Khim. Prir. Soedin., 135 (1997).

  11. Sh. Yu. Islambekov, A. K. Karimdzhanov, A. I. Ismailov, F. G. Kamaev, and A. S. Sadykov, Khim. Prir. Soedin., 46 (1976).

  12. L. Y. Foo, Phytochemistry,20, 1397 (1981).

    Google Scholar 

  13. N. Tanaka, G. Nonaka, and I. Nishioka, Phytochemistry22, 2575 (1983).

    Google Scholar 

  14. G. Nonaka, F. Hsu, and I. Nishioka, J. Chem. Soc., Chem. Commun., No. 15, 781 (1981).

    Google Scholar 

  15. G. Nonaka, I. Nishioka, T. Nagasawa, and H. Oura, Chem. Pharm. Bull.,29, 2862 (1981).

    Google Scholar 

  16. L. J. Porter, R. H. Newmen, L. Y. Foo, and R. W. Hemingway, J. Chem. Soc., Perkin Trans.I, 1217 (1982).

    Google Scholar 

  17. S. Morimoto, H. Tanaka, G. Nonaka, and I. Nishioka, Phytochemistry,27, 907 (1988).

    Google Scholar 

  18. S. Hakomori, J. Biochem. (Tokyo),55, 205 (1964).

    Google Scholar 

Download references

Authors

Additional information

Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Tashkent, fax (3712) 40 64 75. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 819–833, November–December, 1997.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kuliev, Z.A., Vdovin, A.D., Abdullaev, N.D. et al. Study of the catechins and proanthocyanidins ofQuercus robur . Chem Nat Compd 33, 642–652 (1997). https://doi.org/10.1007/BF02249631

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02249631

Keywords

Navigation