A Synthetically Useful Regioselective Epoxide Ring-Opening Procedure
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397919208019093
Reference5 articles.
1. Novel enantioselective synthesis of platelet activating factor and its enantiomer via ring opening of glycidyl tosylate with 1-hexadecanol
2. Approaches to the Total Synthesis of Adrenal Steroids.1 V. 4b-Methyl-7- ethylenedioxy-1,2,3,4,4aα,4b,5,6,7,8,10,10a β-dodecahydrophenanthrene-4 β-ol-1-one and Related Tricyclic Derivatives
3. The Reduction of Terminal Epoxides
4. A Convenient One-Step Synthesis of Glycidyl Ethers
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1. ChemInform Abstract: A Synthetically Useful Regioselective Epoxide Ring-Opening Procedure.;ChemInform;2010-08-20
2. Oxidation of alkenes with hydrogen peroxide, catalyzed by boron trifluoride. Synthesis of vicinal methoxyalkanols;Russian Journal of General Chemistry;2008-04
3. Rapid Ring‐Opening Reactions of Epoxides using Microwave Irradiation;Synthetic Communications;2008-01
4. Mesoporous aluminosilicate promoted alcoholysis of epoxides;Tetrahedron Letters;2007-07
5. Boron Trifluoride Etherate;Encyclopedia of Reagents for Organic Synthesis;2007-03-15
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