Synthesis ofβ-Hydroxy Sulfides via Thiolysis of Epoxides UsingS-Alkylisothiouronium Salts as Thiol Equivalents in Basic Aqueous Medium
Author:
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/cjoc.200990132/fullpdf
Reference69 articles.
1. Synthesis of cyclic sulfides by intramolecular ring opening of epoxides by thiolates generated by nickel complex catalyzed electroreduction of thioacetates
2. Improved procedure for Juliá–Colonna asymmetric epoxidation of α,β-unsaturated ketones: total synthesis of diltiazem and Taxol TM side-chain
3. Fluoro alcohol as reaction medium: one-pot synthesis of β-hydroxy sulfoxides from epoxides
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1. Synthesis and Antioxidant and Antimicrobial Properties of β-Hydroxy Sulfides, Sulfoxides, and Sulfones Derived from Cardanol and Glycerol Derivatives;Journal of the Brazilian Chemical Society;2020
2. β-Hydroxy sulfides and their syntheses;Beilstein Journal of Organic Chemistry;2018-07-05
3. Recent trends in ring opening of epoxides with sulfur nucleophiles;Molecular Diversity;2017-11-14
4. Recent advances in the transformations of cycloalkane-fused oxiranes and aziridines;Tetrahedron;2017-09
5. Odourless Strategy for Deep Eutectic Solvent-Mediated Ring Opening of Epoxides with In Situ Generated S-Alkylisothiouronium Salts;Synlett;2014-04-07
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