Reversibility in Lewis-acid Promoted Reactions of N-Arylcinnamamides

Elliott, Mark Christopher ORCID: https://orcid.org/0000-0003-0132-0818 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

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Abstract

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:	Schools > Chemistry
Subjects:	Q Science > QD Chemistry
Uncontrolled Keywords:	Friedel-Crafts - quinoline - Lewis acid - microwave
Publisher:	Georg Thieme Verlag
ISSN:	0936-5214
Last Modified:	21 Oct 2022 10:20
URI:	https://orca.cardiff.ac.uk/id/eprint/39881

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