Some Reactions of Minor Components of Nucleic Acids

  • N. K. Kochetkov
  • E. I. Budovskii


In the preceding chapters the characteristic chemical reactions of the major and most of the minor components of nucleic acids have been described However, some of the minor components possess unusual chemical properties because their molecules contain functional groups which are not present in other nucleosides. These reactions, which go beyond the classification adopted in this book, will be examined briefly in this chapter.


Manganese Dioxide Thionyl Chloride Purine Nucleoside Pyrimidine Nucleoside Preceding Chapter 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.


  1. 1.
    M. J. Robins, R. H. Hall, and R. Thedford, Biochemistry, 6:1837 (1967).CrossRefGoogle Scholar
  2. 2.
    K. Biemann, S. Tsunakawa, J. Sonnenbichler, H. Feldmann, D. Dutting, and H. G. Zachau, Angew. Chem., 78:600 (1966).CrossRefGoogle Scholar
  3. 3.
    D. M. G. Martin and C. B. Reese, J. Chem. Soc., (C), 1731 (1968).Google Scholar
  4. 4.
    F. Fittler and R. H. Hall, Biochem. Biophys. Res. Comm., 25:441 (1966).CrossRefGoogle Scholar
  5. 5.
    R. W. Chambers, Progr. Nucl. Acid Res., 5:349 (1966).CrossRefGoogle Scholar
  6. 6.
    W. E. Conn, J. Biol. Chem., 235:1488 (1960).Google Scholar
  7. 7.
    A. M. Michelson and W. E. Cohn, Biochemistry, 1:490 (1962).CrossRefGoogle Scholar
  8. 8.
    R. W. Chambers, V. Kurkov, and R. Shapiro, Biochemistry, 2:1192 (1963).CrossRefGoogle Scholar
  9. 9.
    R. W. Chambers and V. Kurkov, Biochemistry, 3:326 (1964).CrossRefGoogle Scholar
  10. 10.
    M. Tomasz, Y. Sanno, and R. W. Chambers, Biochemistry, 4:1710 (1965).CrossRefGoogle Scholar
  11. 11.
    R. E. Cline, R. M. Fink, and K. Fink, J. Am. Chem. Soc., 81:2521 (1959).CrossRefGoogle Scholar
  12. 12.
    B. R. Baker, T. J. Schwan, and D. V. Santi, J. Med. Chem., 9:66 (1966).CrossRefGoogle Scholar
  13. 13.
    R. Brossmer and E. Röhm, Z. Physiol. Chem., 348:1431 (1967).CrossRefGoogle Scholar
  14. 14.
    K. H. Scheit, Chem. Ber., 99:3884 (1966).CrossRefGoogle Scholar
  15. 15.
    R. Brossmer, Angew. Chem., 79:691 (1967).CrossRefGoogle Scholar
  16. 16.
    M. Green, H. Barner, and S. S. Cohen, J. Biol. Chem., 228:621 (1957).Google Scholar
  17. 17.
    K. Iwai and M. Honjo, Chem. Pharm. Bull., 13:7 (1965).CrossRefGoogle Scholar
  18. 18.
    A. Dugaiczyk and J. J. Eyler, J. Biol. Chem., 244:2750 (1969).Google Scholar

Copyright information

© Plenum Publishing Company Ltd. 1972

Authors and Affiliations

  • N. K. Kochetkov
  • E. I. Budovskii

There are no affiliations available

Personalised recommendations