Skip to main content
Log in

New biheterocyclic spiro system — Spiro-[1,4-benzodioxin-2 (3H),2′(3′H)-benzothiazole]

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A convenient preparative method has been developed for obtaining 3′-methylspiro[1,4-benzodioxin-2 (3H),2′(3′H)-benzothiazole], the first representative of biheterocyclic spiro compounds of a new type.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Y. Ohtani and M. Sumimoto,Acta Chem. Scand., Ser. B 36, 613 (1982);Chem. Abstr.,98, 55823 (1983).

    Google Scholar 

  2. M. R. Stillings, C. B. Chapleo, R. C. M. Butler, J. A. Davis, C. D. England, M. Myers, P. L. Myers, N. Twedle, A. P. Welbourn, J. C. Doxey, and C. F. C. Smith,J. Med. Chem.,28, 1054 (1985).

    Article  PubMed  Google Scholar 

  3. P. T. Meinke, S. P. O'Connor, M. H. Fischer, and H. Mrozik,Tetrahedron Lett.,28, 1054 (1985).

    Google Scholar 

  4. I. Kawashima, M. Kotani, H. Ozawa, M. Suzuki, and T. Tai,Int. J. Cancer,58, 263 (1994);Chem. Abstr.,121, 202870 (1994).

    PubMed  Google Scholar 

  5. K. Ding, A. Rosen, A. K. Ray, and G. Magnusson,Glycoconjugate J.,9, 303 (1992);Chem. Abstr.,119, 93266 (1993).

    Article  Google Scholar 

  6. W. Fridrichsen, W. D. Schroer, and R. Schmidt,Ann. Chem., No. 5, 793 (1976);Chem. Abstr.,85, 94292 (1975).

    Google Scholar 

  7. U. Brandt, U. Haase, H. Schaegger, W. von Jagow,DECHEMA Monogr.,129, 27 (1993);Chem. Abstr.,119, 67877 (1993).

    Google Scholar 

  8. L. Daum, G. Keilhauer, H. Sauter, G. Reinhardt, T. Anke, W. Weber, and W. Steglich,German Patent 3905911;Chem. Abstr.,114, 81853 (1991).

    Google Scholar 

  9. L. Daum, G. Keilhauer, T. Anke, W. Weber, W. Steglich, B. Steffan, A, Scherer, E. Ammermann, and G. Lorenz,German Patent 3815484;Chem. Abstr.,113, 189792 (1990).

    Google Scholar 

  10. W. Weber, T. Anke, B. Steffan, and W. Steglich,J. Antibiot.,43, 207 (1990).;Chem. Abstr.,112, 171880 (1990).

    PubMed  Google Scholar 

  11. H. Von Dobeneck, U. Sommer, E. Lippacher, and F. Schnierle,Liebigs Ann. Chem., No. 11, 1934 (1973);Chem. Abstr.,80, 95649 (1973).

    Google Scholar 

  12. M. C. Moureu,Bull. Soc. Chim. France,21, 107 (1899).

    Google Scholar 

Download references

Authors

Additional information

Institute of Organic Chemistry, National Academy of Sciences of the Ukraine, Kiev 253660; e-mail: iochkiev@sovam.com Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1568–1570, November, 1999.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Dzvinchuk, I.B., Lozinsky, M.O. New biheterocyclic spiro system — Spiro-[1,4-benzodioxin-2 (3H),2′(3′H)-benzothiazole]. Chem Heterocycl Compd 35, 1370–1372 (1999). https://doi.org/10.1007/BF02252011

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02252011

Keywords

Navigation