Molecular dynamics simulations of a guaiacyl ?-O-4 lignin model compound: Examination of intramolecular hydrogen bonding and conformational flexibility-Reference-Cited by-同舟云学术

Molecular dynamics simulations of a guaiacyl ?-O-4 lignin model compound: Examination of intramolecular hydrogen bonding and conformational flexibility

Published:2004 Issue:3 Volume:73 Page:301-315
ISSN:0006-3525
Container-title:Biopolymers
language:en
Short-container-title:Biopolymers

Author:

Besombes St�phane,Mazeau Karim

Publisher

Wiley

Subject

Organic Chemistry,Biomaterials,Biochemistry,General Medicine,Biophysics

Reference47 articles.

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3. Stereochemical Assignment of the threo and erythro Forms of 2-(2,6-Dimethoxyphenoxy)-1-(3,4-dimethoxyphenyl)-1,3-propanediol from X-Ray Analyses of the Synthetic Intermediates (Z)-2-(2,6-Dimethoxyphenoxy)-3-(3,4-dimethoxyphenyl)-2-propenoic Acid and threo-2-(2,6-Dimethoxyphenoxy)-3-(3,4-dimethoxyphenyl)-3-hydroxypropanoic Acid.

4. Studies on Lignin Model Compounds of the beta-O-4 Type: Crystal Structures of threo-1-(4-Hydroxy-3,5-dimethoxyphenyl)-2-(2-methoxyphenoxy)-1,3-propanediol and 3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-(2-methoxyphenoxy)-1-propanone--Methanol (1/1).

5. On the stereochemistry of lignin model compounds of the arylglycerol-?-aryl ether type: Crystal structure oferythro-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-(4-hydroxymethyl-2,6-dimethoxyphenoxy)-1,3-propanediol, C20H26O9

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