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Collect. Czech. Chem. Commun. 2004, 69, 1843-1876
https://doi.org/10.1135/cccc20041843

2-Haloethyl 1-Thioglycosides as New Tools in Glycoside Syntheses. Part 1: Preparation, Characteristics, General Reactions

Andreas Krüger, Jutta Pyplo-Schnieders, Hartmut Redlich* and Pär Winkelmann

Organisch-Chemisches Institut der WWU Münster, Corrensstrasse 40, 48149 Münster, Germany

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  • Ibrahim Nada, Alami Mouad, Messaoudi Samir: Recent Advances in Transition‐Metal‐Catalyzed Functionalization of 1‐Thiosugars. Asian J Org Chem 2018, 7, 2026. <https://doi.org/10.1002/ajoc.201800449>
  • Belz Tyson, Williams Spencer J.: A building block approach to the synthesis of a family of S-linked α-1,6-oligomannosides. Carbohydrate Research 2016, 429, 38. <https://doi.org/10.1016/j.carres.2016.04.015>
  • Brachet Etienne, Brion Jean‐Daniel, Alami Mouad, Messaoudi Samir: Stereoselective Palladium‐Catalyzed Alkenylation and Alkynylation of Thioglycosides. Adv Synth Catal 2013, 355, 2627. <https://doi.org/10.1002/adsc.201300419>
  • Beaver Matthew G., Billings Susan B., Woerpel K. A.: Nucleophilic Substitution Reactions of 2‐Phenylthio‐Substituted Carbohydrate Acetals and Related Systems: Episulfonium Ions vs. Oxocarbenium Ions as Reactive Intermediates. Eur J Org Chem 2008, 2008, 771. <https://doi.org/10.1002/ejoc.200700911>
  • Piekutowska Marta, Pakulski Zbigniew: Synthesis of S-glycosyl thiophosphates, thiophosphonates and thiophosphinates by the Michaelis–Arbuzov rearrangement of anomeric thiocyanates. Carbohydrate Research 2008, 343, 785. <https://doi.org/10.1016/j.carres.2007.12.009>
  • Krueger Andreas, Pyplo‐Schnieders Jutta, Redlich Hartmut, Winkelmann Paer: 2‐Haloethyl 1‐Thioglycosides as New Tools in Glycoside Syntheses. Part 1. Preparation, Characteristics, General Reactions. ChemInform 2005, 36. <https://doi.org/10.1002/chin.200512207>