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Synthesis 2006(12): 2053-2063
DOI: 10.1055/s-2006-942372
DOI: 10.1055/s-2006-942372
PAPER
© Georg Thieme Verlag Stuttgart · New York
A Concise Synthesis of Pyrrolo- and Pyrrolidino[1,2-a]quinolin-1-ones via Diels-Alder Reactions of N-Acyliminium Cations with Olefins
Further Information
Received
12 December 2005
Publication Date:
05 May 2006 (online)
Publication History
Publication Date:
05 May 2006 (online)
Abstract
A concise and efficient synthesis of pyrrolo- and pyrrolidino[1,2-a]quinolin-1-ones has been developed. New members of this family can thus be generated via Diels-Alder reactions of olefins with N-acyliminium cations produced, in the presence of BF3·Et2O, from 5-hydroxy-1-arylpyrrol-2-ones and 5-hydroxy-1-arylpyrrolidin-2-ones in moderate to high yields at ambient temperature.
Key Words
N-acyliminium cation - Diels-Alder reaction - alkenes - 5-hydroxy-1-arylpyrrol-2-one - pyrrolo[1,2-a]quinolin-1-one
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