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Synthesis of the beta-1,3-glucan, laminarahexaose: NMR and conformational studies
Kai-For Mo1, Huiqing Li, Joel T Mague
1Department of Chemistry, Tulane University, New Orleans, LA 70118, USA.
Abstract:
The synthesis of laminarahexaose is described. NMR studies of several of the intermediates leading to the beta-1,3-glucan show anomalously small coupling constants for some of the C-1 hydrogens. An X-ray structure for the protected hexasaccharide shows that the small coupling constants are due to some of the glucopyranose rings adopting a twist-boat conformation. The X-ray studies also explain other unexpected NMR observations.
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