4-Nitrophenyl tetra-O-acetyl-β-D-glucopyranoside

Marco Brito-Arias; Diana Cruz-Salazar; Elies Molins

doi:10.1107/S1600536806052317

4-Nitrophenyl tetra-O-acetyl-β-D-glucopyranoside

Marco Brito-Arias, Diana Cruz-Salazar, Elies Molins

Unidad Profesional Interdisciplinaria de Biotecnología (UPIBI)

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Abstract

In the title compound, C₂₀H₂₃NO₁₂, the pyranoside ring adopts a ⁴C₁ chair conformation, with all substituents oriented in equatorial positions. The endocyclic C-O-C angle is in agreement with the geometry of the equatorial glycosidic bond, typical for the β-D-⁴C₁ pyranoside conformation.

Original language	English
Pages (from-to)	o359-o360
Journal	Acta Crystallographica Section E: Structure Reports Online
Volume	63
Issue number	1
DOIs	https://doi.org/10.1107/S1600536806052317
State	Published - Jan 2007

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title = "4-Nitrophenyl tetra-O-acetyl-β-D-glucopyranoside",

abstract = "In the title compound, C20H23NO12, the pyranoside ring adopts a 4C1 chair conformation, with all substituents oriented in equatorial positions. The endocyclic C-O-C angle is in agreement with the geometry of the equatorial glycosidic bond, typical for the β-D-4C1 pyranoside conformation.",

author = "Marco Brito-Arias and Diana Cruz-Salazar and Elies Molins",

year = "2007",

month = jan,

doi = "10.1107/S1600536806052317",

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volume = "63",

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journal = "Acta Crystallographica Section E: Structure Reports Online",

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publisher = "International Union of Crystallography",

number = "1",

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T1 - 4-Nitrophenyl tetra-O-acetyl-β-D-glucopyranoside

AU - Brito-Arias, Marco

AU - Cruz-Salazar, Diana

AU - Molins, Elies

PY - 2007/1

Y1 - 2007/1

N2 - In the title compound, C20H23NO12, the pyranoside ring adopts a 4C1 chair conformation, with all substituents oriented in equatorial positions. The endocyclic C-O-C angle is in agreement with the geometry of the equatorial glycosidic bond, typical for the β-D-4C1 pyranoside conformation.

AB - In the title compound, C20H23NO12, the pyranoside ring adopts a 4C1 chair conformation, with all substituents oriented in equatorial positions. The endocyclic C-O-C angle is in agreement with the geometry of the equatorial glycosidic bond, typical for the β-D-4C1 pyranoside conformation.

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U2 - 10.1107/S1600536806052317

DO - 10.1107/S1600536806052317

M3 - Artículo

SN - 1600-5368

VL - 63

SP - o359-o360

JO - Acta Crystallographica Section E: Structure Reports Online

JF - Acta Crystallographica Section E: Structure Reports Online

IS - 1

ER -

4-Nitrophenyl tetra-O-acetyl-β-D-glucopyranoside

Abstract

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