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Synlett 2003(15): 2341-2344
DOI: 10.1055/s-2003-43336
DOI: 10.1055/s-2003-43336
LETTER
© Georg Thieme Verlag Stuttgart · New York
A Novel Diels-Alder Approach To Heavily Substituted Azasugars
Further Information
Received
29 August 2003
Publication Date:
21 November 2003 (online)
Publication History
Publication Date:
21 November 2003 (online)
Abstract
Diels-Alder cycloaddition of an appropriately substituted 1,4-oxazin-2-one with vinylene carbonate followed by the chemical manipulation of the bridged bicyclic lactone cycloadduct affords a heavily functionalised azasugar ring.
Key words
Diels-Alder - cycloaddition - 2H-1,4-oxazin-2-one - azasugar
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