Skip to main content
Log in

Indole derivatives

XLVII. The product of the transformation of 4-(indol-3-yl)but-1-yl tosylate on a column of silica

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

It has been established that when 4-(indol-3-yl)butan-1-ol is passed through a column containing hydrated silica, 3H-indole-3-spiro-1′-cyclopentane is formed and this then rearranges into tetrahydrocarbazole.

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

Literature cited

  1. V. N. Buyanov and N. N. Suvorov, Trudy MKhTI im. D. I. Mendeleeva, 52, 114, 1967.

    Google Scholar 

  2. J. Pitra, Chem. Listy, 56, 495, 1962.

    Google Scholar 

  3. A. Jackson and P. Smith, Chem. Comm., 6, 264, 1967.

    Google Scholar 

  4. W. Closson, S. Roman, G. Kwiatkowski, and D. Corwin, Tetrahedron Lett., 21, 2271, 1966.

    Google Scholar 

  5. A. Jackson and P. Smith, Tetrahedron, 21, 989, 1965.

    Google Scholar 

  6. H. Fritz and P. Pfaender, Ber., 98, 989, 1965.

    Google Scholar 

  7. N. N. Suvorov and V. E. Golubev, KhFZh, 8, 13, 1967.

    Google Scholar 

  8. Organic Syntheses [Russian translation], IL, Moscow, 4, 450, 1953.

Download references

Author information

Authors and Affiliations

Authors

Additional information

For Communication XLVI see [1].

Translated from Khimiya Geterotsikli-cheskikh Soedinenii, Vol. 6, No. 6, pp. 759–760, June, 1970.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Golubev, V.E., Suvorov, N.N. Indole derivatives. Chem Heterocycl Compd 6, 701–702 (1970). https://doi.org/10.1007/BF00470521

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00470521

Keywords

Navigation