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Tytuł artykułu

Unusual Ozonolysis of Cholesteryl and Androst-5-en-3beta-yl Acetates in the Presence of Primary Amines. Formation of A-nor-3(5--6alfa)abeo-6beta(H)-5-oxo-steroids, Confirmed by X-ray Analysis

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The reaction of cholesteryl acetate with ozone in the presence of amines has been studied. Besides the expected cleavage products, B-seco-ketoaldehyde and its aldol condensation product, 5-hydroxy-6-formyl-B-nor-5_-cholestane derivative, the abnormal product, 3_-acetoxy-A-nor-3(5_6_)abeo-6_(H)-cholestan-5-one is formed as a result of a new, anomalous cleavage of the primary ozonide. The reaction conditions and isolation procedure were optimized for achieving good yield of the abeo-compound. The X-ray crystal structure analysis confirmed the formation of the unusual steroidal skeleton. It appears to be the first crystallographic analysis of the transformed steroid with A-nor-3(5_6_)abeo skeleton. No product resulting from the amine nucleophilic participation in the cleavage of ozonides was observed.
Słowa kluczowe
Rocznik
Strony
921--930
Opis fizyczny
Bibliogr. 28 poz., rys.
Twórcy
autor
  • Faculty of Chemistry, A. Mickiewicz University, Grunwaldzka 6, 60-780 Poznań, Poland
autor
  • Faculty of Chemistry, A. Mickiewicz University, Grunwaldzka 6, 60-780 Poznań, Poland
autor
  • Faculty of Chemistry, A. Mickiewicz University, Grunwaldzka 6, 60-780 Poznań, Poland
  • Faculty of Chemistry, A. Mickiewicz University, Grunwaldzka 6, 60-780 Poznań, Poland
Bibliografia
  • 1. Bailey P.S., in Ozonation in Organic Chemistry, Academic Press, NY, vol. 2, Ch. 7 (1982).
  • 2. Bailey P.S., in Ozonation in Organic Chemistry, Academic Press, NY, vol. 1, a) Ch. 7, b) Ch. 9 (1978),
  • 3. Fremery M.I. and Fields E.K., J. Org. Chem., 29, 2240 (1964).
  • 4. Hon Y.S., Lin S.W., Lu L. and Chen Y.J., Tetrahedron, 51, 5019 (1995). 
  • 5. Schulz M., Becker D. and Rieche A., Angew. Chem, Int. Ed., 548 (1965).
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  • 7. Gumulka J. and Smith L.L., J. Am. Chem. Soc., 105, 1972(1983); Smith L.L., Ezell E.L. and Jaworski K„ Steroids, 61, 401 (1996).
  • 8. Smith L.L., Lipids, 31, 453 (1996) and references cited therein.
  • 9. a) ParyzekZ., MartynowJ. and Swoboda W., J. Chem. Soc., Perkin Trans. 1,1222 (1990); b) Paiyzek Z. and Rychlewska U., J. Chem. Soc., Perkin Trans. 2,2313 (1997) and references cited therein.
  • 10. Ushigoe Y., Satake S., Masuyama A.,Nojima M. and McCullough K.J., J. Chem. Soc., Perkin Trans. 1, 1939(1997).
  • 11. Jaworski K. and Smith L.L., J. Org. Chem., 53, 555 (1988).
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  • 17. a) Martin J., Parker W., Shroot B. and Steward T., J. Chem. Soc. C, 101 (1967); b) Kasai A., Collect. Czech. Chem. Commun., 43,1778 (1978).
  • 18. Snatzke G. and Kinsky K., Tetrahedron, 28, 289 (1972).
  • 19. Marchon J-C. and Ramasseul R., Synthesis, 389 (1989).
  • 20. Hanson J.R. and Terry N., J. Chem. Res. (S), 50 (1998).
  • 21. Nagata W., Narisada M., Wakabayashi T., Hayase Y. and Masayuki M., Chem. Pharm. Bull., 19, 1567 (1971).
  • 22. Alien RH. and Kennard O., Chemical Design Automation News, 8, 1&31-37 (1993).
  • 23. Turner R.B., J Am. Chem. Soc., 72, 579 (1950).
  • 24. Weill-Raynal J., Synthesis, 49 (1969) and references cited therein; Julia S.A., Eschenmoser A., Heuser H. and Tarkey N„ Helv. Chim. Acta, 36, 1885 (1953).
  • 25. Kehrli A.R.H., Taylor D.A.H. and Niven M., J. Chem. Soc., Perkin Trans. I, 2057 (1990).
  • 26. Sheidrick G.M., Acta Cryst., A46, 467 (1990).
  • 27. Sheidrick G.M., SHELXL-97, University of Gottingen, (1997).
  • 28. Stereochemical Workstation Operation Manual, Release 3.4, Siemens Analytical X-Ray Instruments, Inc., Medison, Wisconsin, USA, (1989).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0023-0004
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