A 13c-n.m.r. study of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexo-pyranoses and their O-acetyl and deoxy derivatives

Carbohydrate Research

Volumn 76, Issue 1, 1979, Pages 39-44

  Trnka, Tomáš ^a   Černý, Miloslav ^a   Shmyrina, Anna Ya ^b   Shashkov, Alexander S ^b   Sviridov, Alexander F ^b   Chizhov, Oleg S ^b  

^a CHARLES UNIVERSITY   (Czech Republic)

^b N D ZELINSKY INSTITUTE OF ORGANIC CHEMISTRY   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 0038020837     PISSN: 00086215     EISSN: None     Source Type: Journal    
DOI: 10.1016/0008-6215(79)80004-X     Document Type: Article

References (16)

1. Configurational effects on13C chemical shifts of 1,6-anhydro-hexopyranoses and related compounds. Utility of13C–1H coupling patterns for signal assignments
2. Carbon-13 nuclear magnetic resonance spectra of some epoxides
3. Conformational analysis of some methyl 2,3- and 3,4-anhydroglycopyranosides
4. Synthesen mit anhydrozuckern III. Über die reaktion von 2-O-tosyl-1,6:3,4-dianhydro-β-D-galaktopyranose mit natriumhydroxyd
5. Synthesen mit anhydrozuckern IV. Darstellung von 1,6-2,3-dianhydro-β-D-mannopyranose und ihre isomerisierung zu 1,6-3,4-dianhydro-β-D-altropyranose
6. 1H NMR spectra and the conformation of 1,6 : 2,3- and 1,6 : 3,4-dianhydro-β-D-hexopyranoses and their derivatives
7. Syntheses with anhydro sugars. XIII. Preparation of the deoxy derivatives of the 1,6-anhydro-β-D-hexopyranoses by catalytic reduction of 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses
8. Syntheses with anhydro sugars. XVII. Preparation and reactions of 1,6:2,3-dianhydro-4-deoxy- and 1,6:3,4-dianhydro-2-deoxy-β-D-hexopyranoses with nucleophilic and reducing reagents