Crystal structure of N-(benzyloxycarbonyl)aminoethyl-2,3,4,6-tetra-O-benzoyl-α-D-mannopyranoside: stabilization of the crystal lattice by a tandem network of N-H···O, C-H···O, and C-H···Π interactions

Srinivas, O. ; Muktha, B. ; Radhika, S. ; Guru Row, T. N. ; Jayaramana, N. (2004) Crystal structure of N-(benzyloxycarbonyl)aminoethyl-2,3,4,6-tetra-O-benzoyl-α-D-mannopyranoside: stabilization of the crystal lattice by a tandem network of N-H···O, C-H···O, and C-H···Π interactions Carbohydrate Research, 339 (6). pp. 1087-1092. ISSN 0008-6215

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/j.carres.2004.02.009

Abstract

Single crystal X-ray analysis of an aminoethyl mannopyranoside, namely, N-(benzyloxycarbonyl)aminoethyl-2,3,4,6-tetra-O-benzoyl-α -D-mannopyranoside (1), shows that the compound crystallizes in the monoclinic space group P21, with two molecules in the unit cell. The mannopyranoside unit adopts a distorted 4C1 conformation. An analysis of the intermolecular interactions reveals a tandem network of N-H···O, C-H···O, and C-H···Π interactions responsible for stabilizing the crystal lattice. The single crystal X-ray structure of N-(benzyloxycarbonyl)aminoethyl-2,3,4,6-tetra-O-benzoyl-α -D-mannopyranoside is determined. An analysis of the packing motif reveals that a tandem network of N-H···O, C-H···O, and C-H···Π interactions emerges to stabilize the molecular packing in the solid state.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Carbohydrate; Crystal Structure; Hydrogen Bonding; Mannopyranoside; Weak Interactions
ID Code:66001
Deposited On:20 Oct 2011 07:10
Last Modified:11 Jul 2012 04:12

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