A highly efficient protocol for regioselective ring-opening of epoxides with alcohols, water, acetic acid, and acetic anhydride catalyzed by SbF3
Author:
Affiliation:
1. Faculty of Science, Department of Chemistry, Urmia University, Urmia, Iran
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10426507.2015.1135439
Reference48 articles.
1. Aziridines and Epoxides in Organic Synthesis
2. Unraveling the Mechanism of Epoxide Formation from Sulfur Ylides and Aldehydes
3. Phenol-Containing Macrocyclic Diamides as New Catalysts in the Highly Regioselective Conversion of Epoxides to β-Hydroxy Thiocyanates
4. 2,3-Dichloro-5,6-Dicyano-p-Benzoquinone, an efficient, mild, neutral and highly regioselective catalyst for alcoholysis of epoxides
5. Highly Efficient, Regio- and Stereoselective Alcoholysis of Epoxides Catalyzed with Iron(III) Chloride
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