A New Procedure for the Synthesis of D-Glucosamine alpha-C-Glycosides.

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Abstract

Reaction of (2,3,5-tri-O-benzyl-D-arabinofuranosyl)benzylamine with vinylmagnesium bromide and subsequent mercuriocyclisation of the obtained open-chain product, provides a stereoselective entry to α-C-glycosides of D-glucosamine.

Original languageEnglish
Pages (from-to)297-298
Number of pages2
JournalChemical Communications
Publication statusPublished - 1989

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