| Literature DB >> 8156559 |
C Rochas1, P Potin, B Kloareg.
Abstract
The 13C NMR signals of various even and odd agarose oligosaccharides with either D-galactose or 3,6-anhydro-alpha-L-galactose at the reducing end have been assigned. The chemical shifts in water of the agaro- and the neoagaro-oligosaccharides are compared and the influence of dimethyl sulfoxide on the chemical structure of the agaro-oligosaccharides is reported. The 3,6-anhydro-L-galactose residue at the reducing end of agaro-oligosaccharides is in the hydrated form.Entities:
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Year: 1994 PMID: 8156559 DOI: 10.1016/0008-6215(94)80056-1
Source DB: PubMed Journal: Carbohydr Res ISSN: 0008-6215 Impact factor: 2.104