n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran­oside

The title compound [systematic name: (2R,3R,4S,5R,6R)-2-(acet­oxy­meth­yl)-6-propoxytetra­hydro-2H-pyran-3,4,5-triyl triacetate], C(17)H(26)O(10), was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide and n-propanol. The central ring adopts a chair conformation....

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Detalles Bibliográficos
Autores principales: Mönch, Bettina, Emmerling, Franziska, Kraus, Werner, Becker, Roland, Nehls, Irene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569225/
https://www.ncbi.nlm.nih.gov/pubmed/23424448
http://dx.doi.org/10.1107/S1600536812051495
Descripción
Sumario:The title compound [systematic name: (2R,3R,4S,5R,6R)-2-(acet­oxy­meth­yl)-6-propoxytetra­hydro-2H-pyran-3,4,5-triyl triacetate], C(17)H(26)O(10), was formed by a Koenigs–Knorr reaction of 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide and n-propanol. The central ring adopts a chair conformation. The crystal does not contain any significant inter­actions such as hydrogen bonds.

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