Jump to main content
Jump to site search


Synthesis of N-unsubstituted cycloalkylimines containing a 4 to 8-membered ring

Author affiliations

Abstract

Primary cycloalkylimines with a 4 to 8-membered ring were synthesized by dehydrocyanation of the corresponding α-aminonitriles on solid potassium hydroxide via a vacuum gas–solid reaction. Imine–enamine tautomerism has been demonstrated at room temperature for the most kinetically stable derivatives.

Graphical abstract: Synthesis of N-unsubstituted cycloalkylimines containing a 4 to 8-membered ring

Back to tab navigation

Supplementary files

Publication details

The article was received on 03 Mar 2019, accepted on 12 Apr 2019 and first published on 12 Apr 2019


Article type: Communication
DOI: 10.1039/C9CC01755K
Citation: Chem. Commun., 2019, Advance Article

  •   Request permissions

    Synthesis of N-unsubstituted cycloalkylimines containing a 4 to 8-membered ring

    J. Guillemin, W. Nasraoui and H. Gazzeh, Chem. Commun., 2019, Advance Article , DOI: 10.1039/C9CC01755K

Search articles by author

Spotlight

Advertisements