Hydroxylamine derivatives as nucleophiles in ferrier glycosylation: Synthesis of aminoxy pseudoglycals

dc.contributor.author Raji Reddy, Ch
dc.contributor.author Srinivasa Rao, Y.
dc.contributor.author Pavan Kumar, T.
dc.contributor.author Venkatram Reddy, K.
dc.contributor.author Chandrasekhar, S.
dc.date.accessioned 2022-03-27T08:50:28Z
dc.date.available 2022-03-27T08:50:28Z
dc.date.issued 2008-01-03
dc.description.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. © Georg Thieme Verlag Stuttgart.
dc.identifier.citation Synthesis
dc.identifier.issn 00397881
dc.identifier.uri 10.1055/s-2007-1000828
dc.identifier.uri http://www.thieme-connect.de/DOI/DOI?10.1055/s-2007-1000828
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11914
dc.subject Ferrier glycosylation
dc.subject Hydroxylamines
dc.subject Pseudoglycals
dc.title Hydroxylamine derivatives as nucleophiles in ferrier glycosylation: Synthesis of aminoxy pseudoglycals
dc.type Journal. Article
dspace.entity.type
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