Synthesis of Azomethylene Derivatives of 4-Chloro-5H-1,2,3-dithiazole

Journal of Heterocyclic Chemistry

Volumn 41, Issue 1, 2004, Pages 37-43

  Yarovenko, Vladimir N ^a   Es'kov, Andrey A ^a   Zatonsky, George V ^a   Zavarzin, Igor V ^a   Krayushkin, Mikhail M ^a   Averkiev, Boris B ^b   Antipin, Mikhail Yu ^b  

^a N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

^b A N NESMEYANOV INSTITUTE OF ORGANOELEMENT COMPOUNDS   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

4 CHLORO 5H 1,2,3 DITHIAZOLE DERIVATIVE; AZOMETHYLENE DERIVATIVE; CARBENOID; HETEROCYCLIC COMPOUND; HYDRAZONE DERIVATIVE; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; PROTON NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 1542376078     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570410106     Document Type: Article

References (29)

1. K. Kim, Sulfur Reports, 21, 147 (1998).
2. V. Thiery, C. W. Rees, T. Besson, G. Cottenceau and A-M. Pons, Eur. J. Med. Chem., 33, 149 (1998).
3. H.-S. Lee and K. Kim, Tetrahedron Lett., 39, 5781 (1998).
4. H.-S. Lee and K. Kim, Tetrahedron Lett., 39, 6895 (1998).
5. Y. S. Park and K. Kim, Tetrahedron Lett., 40, 6439 (1999).
6. L. S. Konstantinova and O. A. Rakitin, Tetrahedron, 54, 9639 (1998).
7. T. Besson, M.-J. Dozias, V. Guillard, P. Jacquault, M.-D. Legoy and C. W. Rees, Tetrahedron, 54, 6475 (1998).
8. M.-K. Jeon and K. Kim, Tetrahedron, 55, 9651, (1999).
9. J. Guillard and T. Besson, Tetrahedron, 55, 5139, (1999).
10. V. Beneteau, T. Besson and C. W. Rees, Synth. Commun., 27, 2275 (1997).
11. D. Clark, K. Emayan and C. W. Rees, J. Chem. Soc., Perkin Trans. 1, 77 (1998).
12. P. A. Koutentis and C. W. Rees, J. Chem. Soc., Perkin Trans. 1, 111 (1999).
13. T. Besson, C. W. Rees, D.G. Roe and V. Thiéry, J. Chem. Soc., Perkin Trans. 1, 555 (2000).
14. T. Besson, J. Guillard and C. W. Rees, J. Chem. Soc., Perkin Trans. 1, 563 (2000).
15. T. M. Barclay, A. W. Cordes, R. T. Oakley, K. E. Preuss and R. W. Reed, Chem. Commun., 1039 (1998).
16. H.-S. Lee, Y.-G. Chang and K. Kim, J. Heterocyclic Chem., 35, 659, (1998).
17. R. A. Cox, Bruncel, in, The Chemistry of the Hydrazo, Azo, and Azoxy Groups, ed. S. Patai, Interscience, New York, 1975, part 2, chapter 8, pp. 848-850.
18. Y. P. Kitaev, B. I. Buzykin and T. V. Troepolskaya, Russ. Chem. Rev., 39, 441 (1970).
19. A. F. Strobel, M. L. Whitehouse and D. Offenlegungsschrift 2129864 (1971); Chem. Abstr., 76, 99674b (1972).
20. J. Rody and M. Slongo, Europäische Patentanmeldung 0031302, (1980); Chem. Abstr., 95, 187267u (1981).
21. H. R. Meyer, R. Zweidler and D. Offenlegungsschrift 2539461, (1976); Chem. Abstr., 85, 110108d (1976).
22. R. Mohr and M. Zimmermann, Auslegeschrift 1168437, (1964); Chem. Abstr., 61, 1873f (1964).
23. R. Mohr and M. Zimmermann, Auslegeschrift 1168437, (1964); Chem. Abstr., 61, 1873f (1964).
24. Republique Francaise and Brevet D'invention 1577760, (1969); Chem. Abstr., 72, 100716t (1970).
25. U. Claussen, J. Schroeder and D. Offenlegungsschrift 2210261, (1973); Chem. Abstr., 72, 137160c (1973).
26. K. C. Oh, H. Lee and K. Kim, Tetrahedron Lett., 33, 4963 (1992).
27. H. Schroeder, E. Fisher and M. Michalik, J. Prakt. Chem., 330, 900 (1988).
28. T. Besson, M.-J. Dozias, J. Guillard and C. W. Rees, J. Chem. Soc. Perkin Trans. 1, 3925 (1998).
29. G. M. Sheldrick, SHELXTL-97, Version 5.10, Bruker AXS Inc., Madison, WI-53719, USA.