New route to (−)-frontalin and (−)-malyngolide via epoxyketone rearrangement
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
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3. Preparation of enantiomerically enriched compound using enzymes. Part 3. Enzymic preparation of enantiomerically enriched tertiary .alpha.-benzyloxy acid esters. Application to the synthesis of (S)-(-)-frontalin
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3. Biocatalytic Approach for the Total Synthesis of (-)-Malyngolide and Its C(5)-Epimer;Helvetica Chimica Acta;2016-04
4. Metal-Free, One-Pot, Sequential Protocol for Transforming α,β-Epoxy Ketones to β-Hydroxy Ketones and α-Methylene Ketones;The Journal of Organic Chemistry;2015-01-14
5. Asymmetric Synthesis of the β-Methyl-Substituted Analogues of (+)-Tanikolide and (–)-Malyngolide;Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of α-Aryl Ketones;2015
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