Optically active 2,3-epoxy sulfides as precursors to 3-hydroxy-1,2-dithioethers and 3-hydroxy-1-alkenylthioethers
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Asymmetric Epoxidation of Allylic Alcohols: The Sharpless Epoxidation
2. Homochiral 2,3-epoxy sulfides—powerful new synthetic building blocks providing stereoselective access to 2,3-epoxy sulfoxides, 2,3-dihydroxy sulfoxides and (E)-γ-hydroxy-α,β-unsaturated sulfoxides and sulfones. X-Ray molecular structure of rac-(2R*,3R*)-1-[(S*)-phenylsulfinyl] hexane-2,3-diol
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1. Recent trends in ring opening of epoxides with sulfur nucleophiles;Molecular Diversity;2017-11-14
2. ChemInform Abstract: Optically Active 2,3-Epoxy Sulfides as Precursors to 3-Hydroxy-1,2-dithioethers and 3-Hydroxy-1-alkenylthioethers.;ChemInform;2010-06-12
3. Simple and highly efficient catalyst- and waste-free ring opening of epoxides with Na2S in water;Monatshefte für Chemie - Chemical Monthly;2010-02-26
4. Synthesis ofβ-Hydroxy Sulfides via Thiolysis of Epoxides UsingS-Alkylisothiouronium Salts as Thiol Equivalents in Basic Aqueous Medium;Chinese Journal of Chemistry;2009-04
5. Waste-free thiolysis of epoxide in water with high yield;Journal of the Iranian Chemical Society;2009-03
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