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Protection of Miscellaneous Groups

  • J. F. W. McOmie

Abstract

The protection of certain functional groups, namely amide, cyanide, sulphonic acid, sulphonamide, N-hydroxy, and thioether has not been discussed in previous chapters. Except for the amide group, very few studies have been made on the protection of these groups. The available information is summarized below.

Keywords

Peptide Synthesis Cyanide Group Protective Group Sodium Ethoxide Amino Acid Ester 
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.

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References

  1. 1.
    B. LIBERER, Chem. and Ind., 987 (1961).Google Scholar
  2. 2.
    J. RUDINGER, Angew. Chem., 71, 742 (1959).Google Scholar
  3. 3.
    J. J. KORST, J. D. JOHNSON, K. BUTLER, E. J. BIANCO, L. H. GONOVER, and R. B. WOODWARD, J. Amer. Chem. Soc., 90, 439 (1968).CrossRefGoogle Scholar
  4. 4.
    H. MUXFELDT and W. ROGALSKI, J. Amer. Chem. Soc., 87, 933 (1965).CrossRefGoogle Scholar
  5. 5.
    F. M. CALLAHAN, G. W. ANDERSON, R. PAUL, and J. E. ZIMMERMAN, J. Amer. Chem. Soc., 85, 201 (1963).CrossRefGoogle Scholar
  6. 6.
    S. R. DICKMAN and W. L. WESTCOTT, J. Biol. Chem., 210, 481 (1954).Google Scholar
  7. 7.
    Y. SHIMONISHI, S. SAKAKIBARA, and S. AKABORI, Bull. Chem. Soc. Japan, 35, 1966 (1962).CrossRefGoogle Scholar
  8. 8.
    M. PRYSTAS and F. SORM, Coll. Czech. Chem. Commun., 27, 1578 (1962).Google Scholar
  9. 9.
    M. PRYSTAS and F. SORM, Coll. Czech. Chem. Commun., 30, 537 (1965).Google Scholar
  10. 10.
    S. SAKAKIBARA, Y. SHIMONISHI, Y. KISHIDA, M. OKADA, and H. SUGIHARA, Bull. Chem. Soc. Japan, 40, 2164 (1967).CrossRefGoogle Scholar
  11. 11.
    W. KöNIG and R. GEIGER, Chem. Ber., 103, 2041 (1970).CrossRefGoogle Scholar
  12. 12.
    B. LOEV, M. A. HAAS, and F. DOWALO, Chem. and Ind., 973 (1968).Google Scholar
  13. 13.
    F. WEYGAND, W. STEGLICH, J. BJARNASON, R. AKHTAR, and N. CHYTIL, Chem. Ber., 101, 3623 (1968).CrossRefGoogle Scholar
  14. 14.
    F. WEYGAND, W. STEGLICH, and J. BJARANSON, Chem. Ber., 101, 3642 (1968).CrossRefGoogle Scholar
  15. 15.
    P. PIETTA, F. CHILLEMI, and A. U, Chem. Ber., 101, 3649 (1968).CrossRefGoogle Scholar
  16. 16.
    P. PIETTA and G. S. MARSHALL, Chem. Comm., 650 (1970).Google Scholar
  17. 17.
    R. B. GREENWALD and C. L. ZIRKLE, J. Org. Chem., 33, 2118 (1968).CrossRefGoogle Scholar
  18. 18.
    L. I. KRIMEN and D.J. COTA, Org. Reactions, 17, 213 (1969).Google Scholar
  19. 19.
    A. M. MONRO, J. W. H. WATTHEY, and M. C. WHITING, Personal Communication.Google Scholar
  20. 20.
    M. K. SEIKEL, Org. Synth. Coll. Vol., 3, 262 (1955).Google Scholar
  21. 21.
    W. L. F. ARMAREGO and E, E. TURNER, J. Chem. Soc., 1665 (1956).Google Scholar
  22. 22.
    P. E. FANTA, Chem. Rev., 38, 139 (1946).CrossRefGoogle Scholar
  23. 22a.
    P. E. FANTA, 64, 613 (1964).Google Scholar
  24. 23.
    G. ZVILICHOVSKY, Tetrahedron, 23, 353 (1967).CrossRefGoogle Scholar
  25. 24.
    W. KLÖTZER, Monatsh., 95, 265 (1964).CrossRefGoogle Scholar
  26. 25.
    W. KLÖTZER, Monatsh., 96, 169 (1965).CrossRefGoogle Scholar
  27. 26.
    W. KLÖTZER and M. HERBERZ, Monatsh., 99, 847 (1968).CrossRefGoogle Scholar
  28. 27.
    K. HOFMANN, W. HAAS, M. J. SMITHERS, R. D. WELLS, Y. WOLMAN, N. YANAIHARA, and G. ZANETTI, J. Amer. Chem. Soc., 87, 620 (1965).CrossRefGoogle Scholar
  29. 28.
    B. ISELIN, Helv. Chim. Acta, 44, 61 (1961).CrossRefGoogle Scholar
  30. 29.
    B. GUTTE and R. B. MERRIFIELD, J. Amer. Chem. Soc., 91, 501 (1969).CrossRefGoogle Scholar

Copyright information

© Plenum Publishing Company Ltd 1973

Authors and Affiliations

  • J. F. W. McOmie
    • 1
  1. 1.School of ChemistryUniversity of BristolBristolUK

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