Unusual formation of 2,1-benzisothiazole derivatives

Tetrahedron Letters

Volumn 39, Issue 20, 1998, Pages 3311-3314

  Aqad, Emad ^a   Ellern, Arkady ^a   Khodorkovsky, Vladimir ^a  

^a BEN GURION UNIVERSITY OF THE NEGEV   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

2,1 BENZISOTHIAZOLE DERIVATIVE; ANILINE DERIVATIVE; NITROSO DERIVATIVE; THIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL STRUCTURE; CIS TRANS ISOMERISM; CYCLIZATION; MOLECULAR INTERACTION; SYNTHESIS;

EID: 0032516308     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)00478-X     Document Type: Article

References (20)

1. 1. a) Haucke, G.; Paetzold, R., Eds. Photophysicalische Chemie Indigoider Farbstoffe, Nova Acta Leopoldina, 1978
2. b) Zollinger, H. Color Chemistry, VCH, Weinheim, New York, Basel, Cambridge, 1991, 91
3. 2. a) Ross, D. L. Appl. Optics, 1971, 10, 571;
4. b) Irie, M.; Kato, M. J. Am. Chem.Soc. 1985, 107, 1024;
5. c) Pawlik, A.; Grahn, W.; Reisner, A.; Jons, P. G ; Ernst, L. Angew. Chem. Int. Ed. Engl. 1994, 33, 1966;
6. d) Gompper, R.; Hartmann, K.; Kellner, R.; Polborn, K. Angew. Chem. Int. Ed. Engl 1995, 34, 464;
7. e) Rosengaus, J.; Willner, I. J. Phys. Org. Chem. 1995, 8, 54
8. 3. Fabian, J.; Hartmann, H. Light Absorption of Organic Colorants, Spring-Verlag, Berline, 1980, 115
9. 4. a) Augustin, M.; Dolling, W., Vogt, A. Z. Chem. 1983, 333;
10. b) Dolling, W.; Augustin, M.; Ihrke, R. Synthesis, 1987, 655;
11. c) Tormos, G. V.; Khodorkovsky, V. Yu.; Neilands, O. Ya. Khim. Geterotsikl. Soed. 1989, 276; C.A. 112:77011t;
12. d) Tormos, G. V.; Khodorkovsky, V. Yu, Neilands, O. Ya.; Belyakov, S. V. Tetrahedron, 1992, 48, 6863;
13. e) Sudmaie, I. V.; Khodorkovsky, V. Yu.; Edzinya, A. S.; Neilands, O. Ya. Khim. Geterotsikl. Soed. 1993, 761; C.A. 120:216423j
14. 5 Bezdrik, A.; Friedlander, P. Ber. Dtsch. Chem. Ges. 1908, 41, 375;
15. b) Pummerer, R. ibid. 1911, 44, 338
16. 1)
17. o). The structure was solved by direct methods and refined by least-squares in anisotropic approximation to R = 8.00, Rw = 7.50. All calculations were carried out using the SHELX -76 and SHELX-86 programs. Atomic coordinates, bond lengths and angles and thermal parameters have been deposited at the Cambridge Crystallographic Data Center.
18. 8 Davis, M. Adv. Heterocyclic Chem. 1985, 38, 105
19. 9 Chupakhin, O. N.; Postovskii, I. Ya. Russian Chemical Reviews, 1976, 45, 454;
20. b) Chupakhin, O. N.; Charushin, V. N. Tetrahedron, 1988, 44, 1