Conversion ofN-Acyl-4-phenyl/benzyl-oxazolidine-2-thiones into Thiol Esters in the Presence of EtSH-K2CO3
Author:
Publisher
Wiley
Subject
General Chemistry
Reference19 articles.
1. A Facile Access to Chiral 4-Isopropyl-, 4-Benzyl-, and 4-Phenyloxazolidine-2-thione
2. Asymmetric Aldol Additions with Titanium Enolates of Acyloxazolidinethiones: Dependence of Selectivity on Amine Base and Lewis Acid Stoichiometry
3. Asymmetric Aldol Additions: Use of Titanium Tetrachloride and (−)-Sparteine for the Soft Enolization of N-Acyl Oxazolidinones, Oxazolidinethiones, and Thiazolidinethiones
4. Asymmetric Total Synthesis of Callystatin A: Asymmetric Aldol Additions with Titanium Enolates of Acyloxazolidinethiones
5. An Aldol Approach to the Synthesis of the EF Fragment of Spongistatin 1
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1. MNBA-Mediated β-Lactone Formation: Mechanistic Studies and Application for the Asymmetric Total Synthesis of Tetrahydrolipstatin;The Journal of Organic Chemistry;2012-05-14
2. Liquid-liquid-solid Equilibrium for Two Quaternary Systems Potassium Chloride+Rubidium Chloride+1/2-Propanol+Water at 25 °C;Chinese Journal of Chemistry;2008-12
3. Syntheses and crystal structures of rubidium and cesium 3,5-dinitropyrid-2-onate, 3,5-dinitropyrid-4-onate and 3,5-dinitro-4-pyridone-N-hydroxylate;Journal of Coordination Chemistry;2008-03-20
4. Conversion of N-Acyl-4-phenyl/benzyl-oxazolidine-2-thiones (I) into Thiol Esters (III) in the Presence of EtSH-K2CO3.;ChemInform;2006-02-28
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