Organic reactions in ionic liquids: Oxidative dimerisation of thioamides with phenyliodine(III) diacetate

Journal of Chemical Research - Part S

Volumn , Issue 10, 2003, Pages 618-619

  Yan, Mi ^b   Chen, Zhen Chu ^a,b   Zheng, Qin Guo ^c  

^a ZHEJIANG UNIVERSITY   (China)

^b ZHEJIANG UNIVERSITY   (China)

^c ASTON UNIVERSITY   (United Kingdom)

Author keywords

Ionic liquids; Phenyliodine(III) diacetale; Thioamides

Indexed keywords

1 BUTYLPYRIDINIUM TETRAFLUOROBORATE; 1,2,4 THIADIAZOLE DERIVATIVE; BORIC ACID; IODINE DERIVATIVE; ORGANIC COMPOUND; PHENYLIODINE DIACETATE; PYRIDINIUM DERIVATIVE; ROOM TEMPERATURE IONIC LIQUID; SOLVENT; THIOAMIDE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; DIMERIZATION; DRUG SYNTHESIS; INFRARED SPECTROSCOPY; LIQUID; OXIDATION; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; ROOM TEMPERATURE; TECHNIQUE; TEMPERATURE DEPENDENCE;

EID: 0742288638     PISSN: 03082342     EISSN: None     Source Type: Journal    
DOI: 10.3184/030823403322655842     Document Type: Article

References (36)

1. (a) A. Vargolis, Chem. Soc. Rev. 1981, 10, 371;
2. (b) E.B. Merkushev, Russ. Chem. Rev. 1987, 56, 836;
3. (c) P.J. Stang and V.V. Zhdankin, Chem. Rev., 1996, 96, 1123;
4. (d) P.J. Stang and V.V. Zhdankin, Chem. Rev., 2002, 102, 2523.
5. (a) T. Welton, Chem. Rev., 1999, 99, 2071;
6. (b) P. Wasserscheid and W. Keim, Angew. Chem. Int. Ed. Engl., 2000, 39, 3772;
7. (c) M. Freementle, Chem. Eng. News, 2000, 15, 20;
8. (d) M. Freementle, Chem. Eng. News, 2001, 1, 21;
9. (e) D. Zhao, M. Wu, Y. Kou and E. Min, Catalysis Today., 2002, 74, 157.
10. (a) A. Stark, B.L. Maclean and R.D. Singer, J. Chem. Soc. Dalton Trans., 1996, 63;
11. (b) C.W. Lee, Tetrahedron Lett., 1999, 40, 2461;
12. (c) C.E. Song, W.H. Shim, E.J. Roh and J.H. Choi, Chem. Commun., 2000, 1695.
13. (a) M.J. Earle, P.B. McComackk and K.R. Seddon, Chem. Commun., 1998, 2245;
14. (b) W. Chen, L. Xu, C. Chatterton and J. Xiao, Chem. Commun., 1999, 1247;
15. (c) C.M. Gordon, A. McCluskey, Chem. Commun., 1999, 1431.
16. (a) R.J. Dyson, D.J. Ellis, D.G. Parher and T. Wetton, Chem. Commun. 1999, 25;
17. (b) A.L. Montero, F.K. Zinn, R.F.D. Souzun and J. Dupont, Tetrahedron Asymmetry, 1997, 8, 177;
18. (c) C.A. Adams, M.J. Earle and K.R. Seddon, Chem. Commun., 1999, 1043;
19. (d) R.A. Brown, P. Pollet, E. Mckoon, C.A. Ecker, C.L. Liotta and P.G. Jessop, J. Am. Chem. Soc. 2001, 123, 1254.
20. (a) M.J. Earle, P.B. McMcormack and K.R. Seddon, Green. Chem., 1999, 23;
21. (b) T. Fischer, A. Sethi, T. Welton and J. Woolf, Tetrahedron Lett., 1999, 40, 793;
22. (c) C.E. Song, W.H. Shim, E.J. Roh, S. Lee and J.H. Choi, Chem. Commun., 2001, 1122.
23. C.J. Mathews, P.J. Smith and T. Welton, Chem. Commun., 2000, 1249.
24. (a) F. Kurzer, Adv. Heterocycl. Chem. 1982, 32, 285;
25. (b) H. Sumi and Y. Takahi, Japan Kokai, 1974, 74, 29697;
26. (c) B. Muefit, N. Siegfried and P. Harun, J. Afr. Food. Chem., 1979, 27, 815;
27. (d) T. Teraji, K. Sakane and J. Got, Eur. Pat. Appl. 1981, 27599, CA, 1981,95, P115575.
28. G.C. Owens, M.M. Abu-Omar, J. Mol. Cat. A: Chemical, 2002, 187, 211.
29. (a) W.T.M. EL-Wassing, K.A. Jorgensen and S.O. Laweson, Tetrahedron. 1983, 39, 1729;
30. (b) W.R. Sherman, A. Von. Esch, J. Med. Chem., 1965, 8, 25;
31. (c) M. Bahadn, S. Nitz, H. Parlar and F. Korte, Z. Naturforsch. 1979, 34B, 768;
32. (d) E. Haraki, T. Inaike and E. Imoto, Bull. Chem. Soc. Jpn. 1968, 41, 1361;
33. (e) G. Kresz and A. Maschke, Ger, 1964, 1167816, CA. 1964, 61, 3118f;
34. (f) Y. Takikawa, K. Shimada, K. Sato, S. Sato and S. Takizawa, Bull. Chem. Soc. Jpn. 1985, 58, 995.
35. F. Luciano, L. Andreal, B. Carla, B. C. Anna and S. Paolo, J. Heterocyclic. Chem., 2000, 37, 63.
36. M. Minoru and O. Kazuaki, Tetrahedron Lett., 1984, 25, 409.