Iodide-catalysed cyclization of unsaturated N-chloroamines: A new way to synthesise 3-chloropiperidines - Forschungsportal der Justus-Liebig-Universität Gießen:

Journalartikel

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

Autorenliste: Noack, M; Göttlich, R

Jahr der Veröffentlichung: 2002

Seiten: 3171-3178

Zeitschrift: European Journal of Organic Chemistry

Bandnummer: 2002

Heftnummer: 18

ISSN: 1434-193X

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

Verlag: 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.

Autoren/Herausgeber

- Uni.-Prof. Dr. Richard Göttlich

Zitierstile

Harvard-Zitierstil: 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-Zitierstil: 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