Pyridinium-Ionen in Nachbarschaft zu Oxiranringen: nützliche Zwischenstufen zur stereospezifischen Synthese von β-Hydroxyketonen
Author:
Publisher
Wiley
Subject
General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ange.19961080514/fullpdf
Reference19 articles.
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1. On the Michael Addition of Water to α,β-Unsaturated Ketones Using Amino Acids;European Journal of Organic Chemistry;2013-10-15
2. ChemInform Abstract: Pyridinium Ions Adjacent to Oxirane Rings: Useful Intermediates for the Stereospecific Synthesis of β-Hydoxy Ketones.;ChemInform;2010-08-05
3. Highly Efficient Epoxidation of Olefins Using Aqueous H2O2 and Catalytic Methyltrioxorhenium/Pyridine: Pyridine-Mediated Ligand Acceleration;Journal of the American Chemical Society;1997-07-01
4. Diastereoselective Catalytic Epoxidation of Chiral Allylic Alcohols by the TS-1 and Ti-β Zeolites: Evidence for a Hydrogen-Bonded, Peroxy-Type Loaded Complex as Oxidizing Species;The Journal of Organic Chemistry;1997-05-01
5. Formation of sulfinate esters in the synthesis of triflates;Tetrahedron Letters;1996-11
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