Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Reversibility in Lewis-acid Promoted Reactions of N-Arylcinnamamides

Elliott, Mark Christopher and Wordingham, Stuart V. 2004. Reversibility in Lewis-acid Promoted Reactions of N-Arylcinnamamides. Synlett 2004 (5) , pp. 898-900. 10.1055/s-2004-820024

Full text not available from this repository.


The Lewis-acid promoted cyclisation reactions of N-arylcinnamamides have been investigated. With aluminium ­chloride a range of products were obtained, while much more se­lective cyclisation reactions were observed with bismuth chloride.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Chemistry
Subjects: Q Science > QD Chemistry
Uncontrolled Keywords: Friedel-Crafts - quinoline - Lewis acid - microwave
Publisher: Georg Thieme Verlag
ISSN: 0936-5214
Last Modified: 04 Jun 2017 04:29

Citation Data

Cited 16 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item