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Synthesis 2008(1): 122-126
DOI: 10.1055/s-2007-1000828
DOI: 10.1055/s-2007-1000828
PAPER
© Georg Thieme Verlag Stuttgart · New York
Hydroxylamine Derivatives as Nucleophiles in Ferrier Glycosylation: Synthesis of Aminoxy Pseudoglycals [1]
Further Information
Received
20 July 2007
Publication Date:
07 December 2007 (online)
Publication History
Publication Date:
07 December 2007 (online)
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Abstract
The use of hydroxylamine derivatives as the aminoxy equivalent nucleophiles in Ferrier glycosylation catalyzed by various acid catalysts is described. The reaction of tri-O-protected d-glucal with N-hydroxyphthalimide or N-hydroxysuccinimide was effectively promoted by a catalytic amount of zinc(II) chloride to produce the corresponding aminoxy pseudoglycal in good yields and preferential anomeric selectivity.
Key words
hydroxylamines - Ferrier glycosylation - pseudoglycals
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15This product showed hypolipidemic activity in mice, see ref. 12.