Skip to main content
Log in

Catalytic synthesis of N-alkyloctahydroisoindoles

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Catalytic hydroamination of 1,2-bis-(hydroxymethyl)cyclohexane by aliphatic nitriles over a nickel catalyst yielded a series of N-alkyl-substituted octahydroisoindoles. Conditions for their synthesis were selected. The IR, PMR, and mass spectra and the probable mechanism of formation of these compounds are discussed.

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. William J. Bailey et al., J. Am. Chem. Soc., 75, 4780 (1953).

    Google Scholar 

  2. R. Juday and H. Alkins, J. Am. Chem. Soc., 77, 4559 (1955).

    Google Scholar 

  3. A. Balker, W. Coprez, and W. L. Holstein, Ind. Eng. Chem., Prod. Res. Dev., 22 (1983).

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1619–1622, December, 1990.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kozintsev, S.I., Zhavrid, A.S., Serzhanin, A.I. et al. Catalytic synthesis of N-alkyloctahydroisoindoles. Chem Heterocycl Compd 26, 1346–1348 (1990). https://doi.org/10.1007/BF00473961

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00473961

Keywords

Navigation