Iodide-catalysed cyclization of unsaturated N-chloroamines: A new way to synthesise 3-chloropiperidines - Research portal of Justus Liebig University Giessen:

Journal article

Iodide-catalysed cyclization of unsaturated N-chloroamines: A new way to synthesise 3-chloropiperidines

Authors list: Noack, M; Göttlich, R

Publication year: 2002

Pages: 3171-3178

Journal: European Journal of Organic Chemistry

Volume number: 2002

Issue number: 18

ISSN: 1434-193X

DOI Link: https://doi.org/10.1002/1099-0690(200209)2002:18<3171::AID-EJOC3171>3.0.CO;2-L

Publisher: Wiley

Abstract:
Tetrabutylammonium iodide is a very efficient catalyst for the cyclization of unsaturated N-chloroamines. The catalysis seems to proceed through N-iodoamine intermediates, which act as a source of iodonium ions.

Authors/Editors

- Uni.-Prof. Dr. Richard Göttlich

Citation Styles

Harvard Citation style: Noack, M. and Göttlich, R. (2002) Iodide-catalysed cyclization of unsaturated N-chloroamines: A new way to synthesise 3-chloropiperidines, European Journal of Organic Chemistry, 2002(18), pp. 3171-3178. https://doi.org/10.1002/1099-0690(200209)2002:18<3171::AID-EJOC3171>3.0.CO;2-L

APA Citation style: Noack, M., & Göttlich, R. (2002). Iodide-catalysed cyclization of unsaturated N-chloroamines: A new way to synthesise 3-chloropiperidines. European Journal of Organic Chemistry. 2002(18), 3171-3178. https://doi.org/10.1002/1099-0690(200209)2002:18<3171::AID-EJOC3171>3.0.CO;2-L