Tetrahydrofuran alpha-azido esters: Precursors of anomeric alpha-amino acid monomers via radical bromination

A general route for the synthesis of tetrahydrofuran α-azido esters as the equivalent of monomeric furanose anomeric α-amino acids is described. Highly selective radical bromination of a range of suitably protected carbohydrate C-glycosyl derivatives affords bromo-esters which undergo efficient disp...

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Détails bibliographiques
Auteurs principaux: Smith, M, Long, D, Martin, A, Campbell, N, Bleriot, Y, Fleet, G
Format: Journal article
Langue:English
Publié: 1999