Tytuł artykułu
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Abstrakty
The reaction of 2,2,4,4-tetramethyl-3-thioxocyclobutanone (1) with dimethyl diazomalonate in the presence of Rh2(OAc)4 in toluene at 50_C yielded a mixture of three products 10, 11, and 12. Thiocarbonyl ylide 8 is believed to be the common intermediate. The formation of 10 is rationalized by the 1,3-dipolar electrocyclization of 8 to give spirocyclic thiirane 9, which spontaneously eliminated sulfur. On the other hand, the 1,5- dipolar electrocyclization of 8 led to 1,3-oxathiole 11, which is converted into lactone 12 by hydrolysis.
Wydawca
Czasopismo
Rocznik
Tom
Strony
551--555
Opis fizyczny
Bibliogr. 17 poz., rys
Twórcy
autor
- Section of Heteroorganic Compounds, University of Łódź, Narutowicza 68, PL-90-136 Łódź, Poland
autor
- Section of Heteroorganic Compounds, University of Łódź, Narutowicza 68, PL-90-136 Łódź, Poland
autor
- Organisch-chemisches Institut der Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland
Bibliografia
- 1. Mlostoń G., Romański J., Schmidt Ch., Reisenauer H.P. and Maier G., Chem. Ber., 127, 2527 (1994).
- 2. Mlostoń G. and Heimgartner H., Helv. Chim. Acta, 79, 1785 (1996).
- 3. Mlostoń G., Romański J., Świątek A. and Heimgartner H., Helv. Chim. Acta, 82, 946 (1999).
- 4. Mlostoń G., Romański J. and Heimgartner H., Heterocycles, 50,403 (1999).
- 5. Review on thiocarbonyl ylides: Mlostoń G. and Heimgartner H., Polish J. Chem., 74, 1503 (2000).
- 6. Dawid M., Mlostoń G. and Warkentin J., Org. Lett., 3, 2455 (2001).
- 7. Mlostoń G., Romański J., Linden A. and Heimgartner H., Helv. Chim. Acta, 82, 1302 (1999).
- 8. Dawid M., Warkentin J. and Mlostoń G., Chem. Eur. J., submitted.
- 9. Diebert C.E., J. Org. Chem., 35, 1501 (1970).
- 10. Huisgen R., Mlostoń G., Giera H. and Langhals E., Tetrahedron, in press, and refs, cited therein.
- 11. Huisgen R., Mlostoń G. and Langhals E., Helv. Chim. Acta, 84, 1805 (2001).
- 12. Kagi M., Linden A., Mlostoń G. and Heimgartner H., Helv. Chim. Acta, 81, 285 (1998).
- 13. Kelmendi B., Mlostoń G. and Heimgartner H., Heterocycles, 52,475 (2000).
- 14. Mlostoń G., Romański J., Linden A. and Heimgartner H., Polish J. Chem., 70, 595 (1996).
- 15. Mlostoń G., Romański J., Linden A. and Heimgartner H., Helv. Chim. Acta, 79, 1305 (1996).
- 16. Elam E.U. and Davis H.W., J. Org. Chem., 32, 1562 (1967).
- 17. Peace B.W., Carman F. and Wulfman D.S., Synthesis, 658 (1971).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ1-0020-0058