2,6-diphenyl-4H-chalcogenopyran-4-ones and 2,6-diphenyl-4H- chalcogenopyran-4-thiones: A new catalyst for the Baylis-Hillman reaction

Tetrahedron Letters

Volumn 40, Issue 19, 1999, Pages 3741-3744

  Iwama, Tetsuo ^a   Kinoshita, Hironori ^a   Kataoka, Tadashi ^a  

^a GIFU PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

Baylis Hillman reactions; Thiopyrans; Thiopyrylium ions; Titanium and compounds

Indexed keywords

4 PYRONE DERIVATIVE; CHALCOGEN;

ARTICLE; CATALYSIS; JAPAN; MOLECULAR INTERACTION; SYNTHESIS;

EID: 0033532009     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(99)00585-7     Document Type: Article

References (25)

1. [1] Basavaiah D, Rao PD, Hyma RS. Tetrahedron 1996;52:8001-8062.
2. [2] Drewes SE, Roos GHP. Tetrahedron 1988;44:4653-4670.
3. [3] Ciganek E. Org. React. 1997;51:201-350.
4. [4] Imagawa T, Uemura K, Nagai Z, Kawanisi M. Synth. Commun. 1984;14:1267-1273.
5. [5] Hill JS, Isaacs NS. J. Chem. Research (S) 1988:330-331, (M) 1988:2641-2676.
6. [5] Hill JS, Isaacs NS. J. Chem. Research (S) 1988:330-331, (M) 1988:2641-2676.
7. [6] Roos GHP, Rampersadh P. Synth. Commun. 1993;23:1261-1266.
8. [7] Kundu MK, Mukherjee SB, Balu N, Padmakumar R, Bhat SV. Synlett 1994:444.
9. [8] Auge J, Lubin N, Lubineau A. Tetrahedron Lett. 1994;35:7947-7948.
10. [9] Kündig EP, Xu LH, Romanens P, Bernardinelli G. Tetrahedron Lett. 1993;34:7049-7052.
11. [10] Rafel S, Leahy JW. J. Org. Chem. 1997;62:1521-1522.
12. [11] Aggarwal VK, Tarver GJ, McCague R. J. Chem. Soc., Chem. Commum. 1996:2713-2714.
13. [12] Hayase T, Shibata T, Soai K, Wakatsuki Y. Chem. Commun. 1998:1271-1272.
14. [13] Kawamura M, Kobayashi S. Tetrahedron Lett. 1999;40:1539-1542.
15. [14] Barrett AGM, Cook AS, Kamimura A. Chem. Commun. 1998:2533-2534.
16. [15] Kataoka T, Iwama T, Tsujiyama S. Chem. Commun. 1998:197-198.
17. [16] Kataoka T, Iwama T, Tsujiyama S, Iwamura T, Watanabe S. Tetrahedron 1998;54:11813-11824.
18. [17] Kataoka T, Iwama T, Kinoshita H, Tsujiyama S, Tsurukami Y, Iwamura T, Watanabe S. Synlett 1999:197-198.
19. [18] Kataoka T, Iwama T, Tsujiyama S, Kanematsu K, Iwamura T, Watanabe S. Chem. Lett. 1999:257-258.
20. [19] Traverso G. Chem. Ber. 1958;91:1224-1229.
21. [20] Tolmachev AI. Zh. Obshch. Khim. 1963;33:1864-1870 [CA 1964;60:689].
22. [21] Detty MR, Murray BJ. J. Org. Chem. 1982;47:5235-5239.
23. [22] Detty MR, Murray BJ, Seidler MD. J. Org. Chem. 1982;47:1968-1969.
24. [23] Detty MR, Hassett JW. Tetrahedron 1985;41:4853-4859.
25. [24] Doddi G, Ercolani G. Adv. Heterocycl. Chem. 1994;60:65-195.