Preparation and reactivity of N-substituted S,S,S-triphenyliminosulfonium salts

Chemistry Letters

Volumn , Issue 10, 1998, Pages 1013-1014

  Yoshimura, Toshiaki ^a   Fujii, Takayoshi ^a   Hamata, Kouki ^a   Imado, Masahiro ^a   Morita, Hiroyuki ^a   Ono, Shin ^a   Horn, Ernst ^b  

^a UNIVERSITY OF TOYAMA   (Japan)

^b UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0032263082     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1998.1013     Document Type: Article

References (13)

1. S. Oae, T. Numata, and T. Yoshimura, "The chemistry of the sulphonium group, part 2," ed by C. J. M. Stirling, John Wiley & Sons, New York (1981), pp. 571 and references therin.
2. M. Mori, H. Takeuchi, H. Minato, M. Kobayashi, M. Yoshida, H. Matsuyama, and N. Kamigata, Phosphorus, Sulfur, and Silicon, 47, 157 (1990).
3. a) O. Glemser and R. Mews, Angew. Chem., Int. Ed. Engl., 19, 883 (1980).
4. b) R. Bartsch, H. Henle, T. Meier, and R. Mews, Chem. Ber., 121, 451 (1988).
5. T. Yoshimura, K. Hamada, M. Imado, K. Hamata, K. Tomoda, T. Fujii, H. Morita, C. Shimasaki, S Ono, .E. Tsukurimichi, N. Furukawa, and T. Kimura, J. Org. Chem., 62, 3802 (1997).
6. 5: C, 62.30; H, 4.18; N, 2.91%.
7. 2).
8. H. Oberhammer and W. Zeil, Z. Naturforch., A, 24, 1612 (1969).
9. H. Oberhammer and W. Zeil, Z. Naturforsch., A, 25, 845 (1970).
10. 3 values.
11. -) with aqueous methanolic potassium hydroxide at room temperature for 24 h gave S,S-diphenylsulfone (4) and biphenyl in 92 and 5% isolated yield, respectively.
12. H. Kise, G. F. Whitfield, and D. Swern, J. Org. Chem., 37, 1121 (1972); J. A. Franz and J. C. Martin, J. Am. Chem. Soc., 97, 583 (1975).
13. H. Kise, G. F. Whitfield, and D. Swern, J. Org. Chem., 37, 1121 (1972); J. A. Franz and J. C. Martin, J. Am. Chem. Soc., 97, 583 (1975).