Polysaccharides 1985
DOI: 10.1007/978-1-349-06369-7_1
|View full text |Cite
|
Sign up to set email alerts
|

Nuclear magnetic resonance studies of polysaccharide structure and interactions

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
8
0

Year Published

1988
1988
2022
2022

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 8 publications
(8 citation statements)
references
References 144 publications
0
8
0
Order By: Relevance
“…Such a shift has also been observed in other polysaccharides when substitution with sulphated groups occurred. 19 The signals relative to glucosamine (69É9 ppm), C 4 and glucuronic (73É0 ppm) and (74É1 ppm) show C 2 C 3 little variation of chemical shifts or of intensity, which indicates that a partial substitution may involve these positions.…”
Section: Sulphated Hyal Derivativesmentioning
confidence: 98%
“…Such a shift has also been observed in other polysaccharides when substitution with sulphated groups occurred. 19 The signals relative to glucosamine (69É9 ppm), C 4 and glucuronic (73É0 ppm) and (74É1 ppm) show C 2 C 3 little variation of chemical shifts or of intensity, which indicates that a partial substitution may involve these positions.…”
Section: Sulphated Hyal Derivativesmentioning
confidence: 98%
“…1) of this fraction corresponded to that of a carbohydrate structure that had no nonsugar substituents and only one kind of anomeric proton. The chemical shift (4.9 ppm) of the signal that arose from the anomeric proton indicated a beta-anomeric configuration (8 LPS. We extracted LPS by the method of Darveau and Hancock (11), which was found to give high yields of both the smooth and rough types of LPS.…”
mentioning
confidence: 99%
“…Those are complex spectra due to the nature of the studied material. The main signals can be assigned to the saccharide matrix carbons (Fernandez, Reguera, & Ortiz, 2001) but the broad one at 173.53 ppm is mainly due to the carbonyl groups of uronic acids (Casu, 1985). When this signal is decomposed (see Fig.…”
Section: Acidic Character Of the Corn Hull And Its Capacity For Ca Rementioning
confidence: 98%