Skip to main content
SpringerLink
Log in

The tritylation of indole

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Contrary to information in the literature, the reaction of indole with chlorotriphenylmethane forms not N-tritylindole but β-tritylindole.

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

Access this article

Log in via an institution

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

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

Literature cited

  1. E. Funakubo and T. Hirotani, Ber., 69, 2123 (1936).

    Google Scholar 

  2. A. P. Terent'ev, A. N. Kost, and V. A. Smit, ZhOKh, 26, 557 (1956).

    Google Scholar 

  3. A. P. Terent'ev, A. N. Kost, and V. A. Smit, ZhOKh, 25, 1959 (1955).

    Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Vil'nyus State Pedagogic Institute, Vil'nyus State University, USSR

    P. F. Butskus & N. V. Raguotene

Authors
  1. P. F. Butskus
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. N. V. Raguotene
    View author publications

    You can also search for this author in PubMed Google Scholar

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, Vol. 6, No. 8, pp. 1056–1057, August, 1970.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Butskus, P.F., Raguotene, N.V. The tritylation of indole. Chem Heterocycl Compd 6, 983–984 (1970). https://doi.org/10.1007/BF00480629

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00480629

Keywords

Search

Navigation