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Collect. Czech. Chem. Commun. 1985, 50, 1176-1183
https://doi.org/10.1135/cccc19851176

29Si (and 13C) NMR spectra of all pertrimethylsilylated O-acetyl and O-benzoyl 1,6-anhydro-β-D-glucopyranose derivatives. A test of empirical assignment rules

Jan Schramla, Štefan Kučárb, Jan Zelenýa and Václav Chvalovskýa

a Institute of Chemical Process Fundamentals, Czechoslovak Academy of Sciences, 165 02 Prague 6-Suchdol
b Institute of Chemistry, Slovak Academy of Sciences, 842 38 Bratislava

Crossref Cited-by Linking

  • Harket Mouna, De Jeso Bernard, Lartigue Jean-Claude, Petraud Michel, Ratier Max: Application of the 29Si NMR 2D INEPT spin-flip J-resolved technique to the structural analysis of trimethylsilylated glycosides. Carbohydrate Research 1994, 263, 155. <https://doi.org/10.1016/0008-6215(94)00163-4>
  • Schraml Jan: 29Si N M R spectroscopy of trimethylsilyl tags. Progr Nucl Magn Reson Spectrosc 1990, 22, 289. <https://doi.org/10.1016/0079-6565(90)80010-F>
  • Schraml J., Petráková E., Hirsch J.: 29Si and 13C NMR spectra of all possible pertrimethylsilylated β‐D‐xylopyranosyl‐substituted methyl 4‐O‐β‐D‐xylopyranosyl‐β‐D‐xylopyranosides assigned by 2D heteronuclear 1H‐29Si and 1H‐13C chemical shift correlations. Magnetic Reson in Chemistry 1987, 25, 75. <https://doi.org/10.1002/mrc.1260250118>