Copper(I)-catalyzed intramolecular addition of N-chloroamines to double bonds under aprotic conditions. Towards a stereoselective catalytic radical reaction - Forschungsportal der Justus-Liebig-Universität Gießen:

Journalartikel

Copper(I)-catalyzed intramolecular addition of N-chloroamines to double bonds under aprotic conditions. Towards a stereoselective catalytic radical reaction

Autorenliste: Göttlich, R

Jahr der Veröffentlichung: 2000

Seiten: 1561-1564

Zeitschrift: Synthesis: Journal of Synthetic Organic Chemistry

Bandnummer: 11

ISSN: 0039-7881

DOI Link: https://doi.org/10.1055/s-2000-7605

Verlag: Thieme Publishing / Georg Thieme Verlag

Abstract:
Copper(I) complexes catalyze the intramolecular addition of N-chloramines to carbon-carbon double bonds under neutral conditions, a reaction that proceeds via a metal complexed aminyl radical. A high diastereoselectivity is obtained in the cyclization step due to the sterically demanding copper complex.

Autoren/Herausgeber

- Uni.-Prof. Dr. Richard Göttlich

Zitierstile

Harvard-Zitierstil: Göttlich, R. (2000) Copper(I)-catalyzed intramolecular addition of N-chloroamines to double bonds under aprotic conditions. Towards a stereoselective catalytic radical reaction, Synthesis: Journal of Synthetic Organic Chemistry, 11, pp. 1561-1564. https://doi.org/10.1055/s-2000-7605

APA-Zitierstil: Göttlich, R. (2000). Copper(I)-catalyzed intramolecular addition of N-chloroamines to double bonds under aprotic conditions. Towards a stereoselective catalytic radical reaction. Synthesis: Journal of Synthetic Organic Chemistry. 11, 1561-1564. https://doi.org/10.1055/s-2000-7605