Halogen exchange reaction of optically pure halotelluranes

Heterocycles

Volumn 46, Issue 1, 1997, Pages 373-384

  Takahashi, Shigemasa ^a   Zhang, Jian ^a   Saito, Shinichi ^a   Koizumi, Toru ^a  

^a UNIVERSITY OF TOYAMA   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0001564748     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/com-97-s31     Document Type: Article

References (19)

1. G. H. Posner, 'The Chemistry of Sulphones and Sulfoxides', eds. by S. Patai, Z. Rappoport, and C. J., M. Stirling, John Wiley & Sons, Inc., Chichester, 1988.
2. C. Paulmier, 'Selenium Reagents and Intermediates in Organic Synthesis', Pergamon Press, Inc., New York, 1986.
3. Recently, Kamigata et al. reported the preparation of optically active telluronium salts and telluronium ylides. See, T. Shimizu, T. Urakubo, and N. Kamigata, Chem. Lett., 1996, 297.
4. T. Shimizu, T. Urakubo, and N. Kamigata, J. Org. Chem., 1996, 61, 8032.
5. N. Kamigata, A. Matsuhisa, H. Taka, and T. Shimizu, J. Chem. Soc., Perkin Trans, I, 1995, 821.
6. Y. Arai, M. Matsui, T. Kontani, and T. Koizumi, J. Chem. Soc., Perkin Trans. I, 1994, 15.
7. Y. Arai, M. Matsui, A. Fujii, T. Kontani, T. Ohno, T. Koizumi, and M. Shiro, J. Chem. Soc., Perkin Trans. 1, 1994, 25.
8. Y. Arai, and T. Koizumi, Sulfur Reports, 1993, 15, 41.
9. Y. Arai, and T. Koizumi, Rev. Heteroatom Chem., 1992, 6, 202.
10. T. Takahashi, N. Kurose, S. Kawanami, Y. Arai, and T. Koizumi, J. Org. Chem., 1994, 59, 3262.
11. T. Takahashi, N. Kurose, S. Kawanami, A. Nojiri, Y. Arai, T. Koizumi, and M. Shiro, Chem. Lett., 1994, 59, 3262.
12. N. Kurose, T. Takahashi, and T. Koizumi, J. Org. Chem., 1996, 61, 2932.
13. T. Takahashi, J. Zhang, N. Kurose, S. Takahashi, T. Koizumi, and M. Shiro, Tetrahedron: Asymmetry, 1996, 10, 2797.
14. N. Poth, Rev. Tech. Litxemb., 1976, 68, 195
15. (Chem. Abstr., 1977, 87, 135965k).
16. See experimental section for the crystallographic data for 2a.
17. There were six fragments of 2a in a unit cell of the crystal structure. Therefore, six different bond lengths were observed.
18. N. S. Isaacs, 'Physical Organic Chemistry1, Longman Scientific & Technical, Essex, 1987, pp. 239-242.
19. L. Engeman and J. Persson, J. Organomet. Chem., 1990, 388, 71.