Dde as a protecting group for carbohydrate synthesis


Autoria(s): Bornaghi, L.; Dekany, G.; Drinnan, N. B.; Taylor, S.; Toth, I.; West, M. L.
Data(s)

01/01/2006

Resumo

Oligosaccharide synthesis using aminosugars requires the presence of a suitable amino protecting group. A number of protecting groups are currently used, and while many display favorable properties, most agents available still suffer from certain disadvantages. This report details the use of a hydrazine labile aminosugar protecting group, N -[1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl] (Dde), which can be introduced and removed in a facile and cost-effective manner.

Identificador

http://espace.library.uq.edu.au/view/UQ:81618

Idioma(s)

eng

Publicador

Taylor & Francis

Palavras-Chave #Biochemistry & Molecular Biology #Chemistry, Organic #Carbohydrates #Vinylogous Amides #Protecting Group #Solid-phase Synthesis #Oligosaccharide Synthesis #Linked Disaccharides #Building-blocks #Glycosyl Donors #D-glucosamine #Derivatives #2-amino-2-deoxy-d-glucopyranose #Trichloroacetimidate #Units #C1 #250301 Organic Chemical Synthesis #780103 Chemical sciences
Tipo

Journal Article