Conformational Analysis of Neocarrabiose and its Sulfated and/or Pyruvylated Derivatives using the MM3 Force-Field-Reference-Cited by-同舟云学术

Conformational Analysis of Neocarrabiose and its Sulfated and/or Pyruvylated Derivatives using the MM3 Force-Field

Published:2000-01-01 Issue:9 Volume:19 Page:1115-1130
ISSN:0732-8303
Container-title:Journal of Carbohydrate Chemistry
language:en
Short-container-title:Journal of Carbohydrate Chemistry

Author:

Stortz Carlos A.¹²,Cerezo Alberto S.¹²

Affiliation:

1. a Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales , Universidad de Buenos Aires , Pabellón 2, 1428 Buenos Aires, Argentina

2. b Departamento de Química Orgánica, Facultad de Ciencias Exactas y Naturales , Universidad de Buenos Aires , Pabellón 2, 1428 Buenos Aires, Argentina

Publisher

Informa UK Limited

Subject

Organic Chemistry,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/07328300008544138

Reference33 articles.

1. Stortz , C. A. Cases , M. R. and Cerezo , A. S. 1997. Techniques in Glycobiology, Edited by: Townsend , R. R. and Hotchkiss , A. T. Jr . 567New York: Marcel Dekker.

2. A force-field study of the conformational characteristics of the iduronate ring

3. Insights into stereochemical features of sulphated carbohydrates: X-ray crystallographic and modelling investigations

4. Computer modelling of sulfated carbohydrates: Applications to carrageenans

5. Molecular structure of 3-O-(3,6-anhydro-α-d-galactopyranosyl)-β-d-galactopyranose (neocarrabiose) in the solid state and in solution: an investigation by X-ray crystallography, n.m.r. spectroscopy, and molecular mechanics calculations

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