Article ID Journal Published Year Pages File Type
5269882 Tetrahedron Letters 2014 8 Pages PDF
Abstract
Herein we report the synthetic strategy towards the pyran core of macrolactin 3 via Sharpless epoxidation, titanium(IV) mediated regioselective ring-opening reaction of epoxyallyl alcohol/epoxy alcohol and oxa-Michael addition as the key steps.
Keywords
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
Regioselective nucleophilic ring-opening reaction of chiral epoxyallyl alcohols: a ready access to the pyran core of macrolactin 3
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