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Collect. Czech. Chem. Commun. 2006, 71, 311-336
https://doi.org/10.1135/cccc20060311

1,6-Anhydro-1-thio-β-D-glucopyranose (Thiolevoglucosan) and the Corresponding Sulfoxides and Sulfone

Miloš Buděšínskýa,*, Jana Polákováb, Michaela Hamerníkovác, Ivana Císařovád, Tomáš Trnkab and Miloslav Černýb

a Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 166 10 Prague 6, Czech Republic
b Department of Organic Chemistry, Faculty of Science, Charles University, 128 40 Prague, Czech Republic
c Department of Biophysics and Physical Chemistry, Charles University, 500 05 Hradec Králové, Czech Republic
d Department of Inorganic Chemistry, Faculty of Science, Charles University, 128 40 Prague, Czech Republic

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  • Aitken R. Alan, Lightfoot Philip, Thomas Andrew W.: Synthesis, structure and reactivity of some chiral benzylthio alcohols, 1,3-oxathiolanes and their S-oxides. Journal of Sulfur Chemistry 2020, 41, 369. <https://doi.org/10.1080/17415993.2020.1754418>
  • Aitken R. Alan, Henderson Sarah, Slawin Alexandra M. Z.: Structure and thermal reactivity of some 2-substituted 1,3-oxathiolane S-oxides. Journal of Sulfur Chemistry 2018, 39, 422. <https://doi.org/10.1080/17415993.2018.1449844>
  • Dračínský M., Pohl R., Slavětínská L., Hřebabecký H., Buděšínský M.: The determination of sulfoxide configuration in five-membered rings using NMR spectroscopy and DFT calculations. Tet Asymm 2011, 22, 1797. <https://doi.org/10.1016/j.tetasy.2011.10.010>
  • Pedersen Christian M., Marinescu Lavinia G., Bols Mikael: Glycosyl donors in “unusual” conformations – influence on reactivity and selectivity. Comptes Rendus. Chimie 2010, 14, 17. <https://doi.org/10.1016/j.crci.2010.03.030>
  • Aversa Maria Chiara, Barattucci Anna, Bonaccorsi Paola: Glycosulfoxides in carbohydrate chemistry. Tetrahedron 2008, 64, 7659. <https://doi.org/10.1016/j.tet.2008.05.051>