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Synlett 2004(5): 0898-0900
DOI: 10.1055/s-2004-820024
DOI: 10.1055/s-2004-820024
LETTER
© Georg Thieme Verlag Stuttgart · New York
Reversibility in Lewis-acid Promoted Reactions of N-Arylcinnamamides
Further Information
Received
8 January 2004
Publication Date:
10 March 2004 (online)
Publication History
Publication Date:
10 March 2004 (online)
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.
Key words
Friedel-Crafts - quinoline - Lewis acid - microwave
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