Photochemical Oxidation of 1,3-Dithianes with tert-Butyl Hydroperoxide (TBHP)

Habibi, M.; Tangestaninejad, S.; Montazerozohori, M.

Artykuł - szczegóły

Tytuł artykułu

Photochemical Oxidation of 1,3-Dithianes with tert-Butyl Hydroperoxide (TBHP)

Autorzy

Habibi M. , Tangestaninejad S. , Montazerozohori M.

Identyfikatory

Warianty tytułu

Języki publikacji

Abstrakty

A variety of 1,3-dithianes deprotected to their corresponding carbonyl compounds in good to excellent yields in mild and efficient photo-oxidative method using tert-butyl hydroperoxide.

Słowa kluczowe

photochemical oxidation dithiane carbonyl compound tert-butyl hydroperoxide

Wydawca

Polskie Towarzystwo Chemiczne

Czasopismo

Polish Journal of Chemistry

Rocznik

2004

Tom

Vol. 78 / nr 2

Strony

201--204

Opis fizyczny

Bibliogr. 24 poz., rys.

Twórcy

autor

Habibi M.

Department of Chemistry, The University of Isfahan, Isfahan 81745-117, Iran

autor

Tangestaninejad S.

Department of Chemistry, The University of Isfahan, Isfahan 81745-117, Iran

autor

Montazerozohori M.

Department of Chemistry, The University of Isfahan, Isfahan 81745-117, Iran

Department of Chemistry, The University of Isfahan, Isfahan 81745-117, Iran

Bibliografia

1. (a) Satchell D.P.N. and Satchell R.S., Chem. Soc. Rev., 19,55 (1990); (b) Greene T.W. and Wuts P.G.M., Protecting Groups in Organic Synthesis, 3rd ed.; Wiley: NY, 329 (1999).
2. (a) Seebach D„ Synthesis, 17 (1969); (b) Groebei B-T. and Seebach D., Synthesis, 357 (1977).
3. Lee S.W. and Dougherty G„ J. Org. Chem., 5, 81 (1940).
4. Chivers J.C.A. and Smile S., J. Chem. Soc., 697 (1928).
5. Russell G.A. and Ochrymowycz L.A., J. Org. Chem., 34, 3618 (1969).
6. Corey E.J. and Erickson B.W., J. Org. Chem., 36(23), 3553 (1971).
7. Schmittel M. and Levis M., Synlett, 315 (1996).
8. Platen M. and Steckhan E, Chem. ber., 117, 1679 (1984).
9. (a) Kamata M., Kato Y. and Hasegawa E., Tetrahedron Lett., 32,4349 (1991); (b) Kamata M., Sato M. and Hasegawa E., Tetrahedron Lett., 33,5085 (1992); (c) Kamata M., Murakami Y„ Tamagawa M., Kato M. and Hasegawa E., Tetrahedron, 50, 12821 (1994).
10. Liu J. and Wong C-H., Tetrahedron Lett., 43,4037 (2002).
11. Wu Y., Shen X., Huang J.-H., Tang C-J., Liu H.-H. and Hu Q., Tetrahedron Lett., 43, 6443 (2002).
12. Barhate N.B., Shide P.D., Mahajan V.A. and Wakharkar R.D., Tetrahedron Lett., 43, 6031 (2002).
13. Barhate N.B., Gajare A.S., Wakharkar R.D. and Bedekar A.V., Tetrahedron, 55, 11127 (1999).
14. Barhate N.B., Gajare A.S., Wakharkar R.D. and Bedekar A.V., Tetrahedron Lett., 39, 6349 (1998).
15. Barhate N.B., Gajare A.S., Sudalai A. and Wakharkar R.D., Tetrahedron Lett., 38, 653 (1997).
16. Barhate N.B., Gajare A.S., Sudalai A. and Wakharkar R.D., Tetrahedron Lett., 37, 2067 (1996).
17. Habibi M.H. and Mallouk T.E., J. Fluorine Chemistry, 51, 291 (1991).
18. Habibi M.H. and Farhadi S., Tetrahedron Lett., 40, 2821 (1999).
19. Habibi M.H. and Farhadi S., J. Chem. Research, 776 (1998).
20. Porter Q.N., Utley J.H.P., Machion P.D., Pardini V.L., Schumacher P.R. and Viertler H., J. Chem. Soc. Perkin Trans. 1, 973 (1984).
21. Dictionary of organic compounds, 6th., Chapman and Hall: London, 1982.
22. (a) Firouzabadi H., Iranpoor N. and Karimi B., Synthesis, 58 (1999); (b) Seebach D. and Corey E.J., J. Org. Chem., 40,231 (1975); (c) Hatch R.P., Shringarpure J.S. and Weinreb M., J. Org. Chem., 43,4172 (1978); (d) Marshall J.A. and Belletire J.L., Tetrahedron Lett., 12 (13) 871 (1971).
23. Meskens F.A.J., Synthesis, 501 (1981).
24. Milas N.A. and Surgenor D.M., J. Chem. Soc., 68, 208 (1946).

Typ dokumentu

Bibliografia

Identyfikator YADDA

bwmeta1.element.baztech-article-BUJ1-0023-0160