Although many stereochemical features of vitamin D and its ieomeric precursor6 may be coneidered rather well established (1,2) by now, there remain a few intriguing questions. One of the problems that asked for further study, is concerned with the conformational analysis of tachyeterol (Fig. I). The
2D-N.M.R. studies of the related bacterial polysaccharides K54 and XM6
β Scribed by Ian J. Colquhoun; Victor J. Morris; Ian W. Sutherland
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 808 KB
- Volume
- 187
- Category
- Article
- ISSN
- 0008-6215
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β¦ Synopsis
2D-N.m.r. (COSY) spectra of tetrasaccharides derived from the bacterial polysaccharides K54, produced by Klebsiella aerogenes serotype K54, and XM6 (from Enterobacter NCIB 11870) have enabled full assignment of the 'H-n.m.r. spectra. The 2D spectra, together with n.0.e. experiments, indicate that the Oacetyl group of K54 is located at O-2 of the L-fucose residue. The 13C-n.m.r. spectra of the polysaccharides have been assigned with the help of 2D-13C/'H shift-correlation methods.
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Sequential tritylation, benzoylation, and detritylation of methyl 3-deoxy-3fluoro-AD-galactop~~oside gave crystalline methyl 2,4-di-O-benzoyl-3-deoxy-3-~uoro-ED-gala~opyr~oside (9), which was used as the initial nucleophile in the synthesis of the target otigosaccha~de (16). Treatment of 9 with 2,3,
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
Reaction of j?-D-allopyranose with acetic anhydride (7.5 mol)-sodium acetate at room temperature and chromatography of the products gave the known' crystalline /Spyranose penta-acetate (5, 36%), together with the hitherto unknown /Spyranose 1,3,4,6 (1, 21%) and 1,2,3,6-tetra-acetate (2, 12%).