Diols obtained via chemo and regioselective ring opening of epoxy alcohols: a straightforward synthesis of 2S,3S-Octandiol
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. The first practical method for asymmetric epoxidation
2. Enantioselective epoxidation of unfunctionalized olefins catalyzed by salen manganese complexes
3. A highly regioselective conversion of epoxides to halohydrins by lithium halides
4. Mild and stereocontrolled synthesis of iodo- and bromohydrins by halogen-tetrakis(isopropoxy)titanium opening of epoxy alcohols
5. Reductive ring openings of allyl-alcohol epoxides
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