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Synthesis 2004(15): 2550-2554
DOI: 10.1055/s-2004-831179
DOI: 10.1055/s-2004-831179
PAPER
© Georg Thieme Verlag Stuttgart · New York
Baylis-Hillman Reaction Assisted Synthesis of Substituted 5,8-Dihydroisoxazolo[4,5-c]azepin-4-ones: A Novel Isoxazole-Annulated Heterocycle [1]
Further Information
Received
21 May 2004
Publication Date:
19 August 2004 (online)
Publication History
Publication Date:
19 August 2004 (online)
Abstract
The novel synthesis of a new isoxazole-annulated heterocycle namely, 5,8-dihydroisoxazolo[4,5-c]azepin-4-one, described herein is based on the reaction of benzylamine with acetates of Baylis-Hillman adducts generated from 3-aryl-5-formyl-isoxazole-4-carboxylate.
Key words
Baylis-Hillman reaction - acetates - 3-aryl-5-formyl-isoxazole-4-carboxylates - 5,8-dihydroisoxazole[4,5-c]azepine-4-ones
CDRI Communication No 6510.
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References
CDRI Communication No 6510.