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n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran-oside.

Mönch B, Emmerling F, Kraus W, Becker R, Nehls I - Acta Crystallogr Sect E Struct Rep Online (2013)

Bottom Line: THE TITLE COMPOUND [SYSTEMATIC NAME: (2R,3R,4S,5R,6R)-2-(acet-oxy-meth-yl)-6-propoxytetra-hydro-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 inter-actions such as hydrogen bonds.

View Article: PubMed Central - HTML - PubMed

Affiliation: BAM Federal Institute for Materials Research and Testing, Department of Analytical Chemistry, Reference Materials, Richard-Willstätter-Strasse 11, D-12489 Berlin, Germany.

ABSTRACT
THE TITLE COMPOUND [SYSTEMATIC NAME: (2R,3R,4S,5R,6R)-2-(acet-oxy-meth-yl)-6-propoxytetra-hydro-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 inter-actions such as hydrogen bonds.

No MeSH data available.


Related in: MedlinePlus

View of the unit cell of the title compound along the a axis.
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Fap2: View of the unit cell of the title compound along the a axis.


n-Propyl 2,3,4,6-tetra-O-acetyl-β-d-glucopyran-oside.

Mönch B, Emmerling F, Kraus W, Becker R, Nehls I - Acta Crystallogr Sect E Struct Rep Online (2013)

View of the unit cell of the title compound along the a axis.
© Copyright Policy - open-access
Related In: Results  -  Collection

License
Show All Figures
getmorefigures.php?uid=PMC3569225&req=5

Fap2: View of the unit cell of the title compound along the a axis.
Bottom Line: THE TITLE COMPOUND [SYSTEMATIC NAME: (2R,3R,4S,5R,6R)-2-(acet-oxy-meth-yl)-6-propoxytetra-hydro-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 inter-actions such as hydrogen bonds.

View Article: PubMed Central - HTML - PubMed

Affiliation: BAM Federal Institute for Materials Research and Testing, Department of Analytical Chemistry, Reference Materials, Richard-Willstätter-Strasse 11, D-12489 Berlin, Germany.

ABSTRACT
THE TITLE COMPOUND [SYSTEMATIC NAME: (2R,3R,4S,5R,6R)-2-(acet-oxy-meth-yl)-6-propoxytetra-hydro-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 inter-actions such as hydrogen bonds.

No MeSH data available.


Related in: MedlinePlus