Asymmetric oxidation of silyl enol ethers using chiral dioxiranes derived from α-fluoro cyclohexanones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference16 articles.
1. A three-step, highly enantioselective synthesis of (R)-2-methyl tryptophane ethyl ester: Comparison with chemical resolution
2. Synthesis of (+)-(R)-methyl 2-aminotetraline-2-carboxylate: the hydroxypinanone method versus the bislactim method
3. A chiral 1,4-oxazin-2-one: asymmetric synthesis versus resolution, structure, conformation and VCD absolute configuration
4. Highly enantioselective epoxidation of enol silyl ethers and esters
5. Asymmetric Epoxidation oftrans-Olefins via Chiral Dioxiranes: A Possible Contribution ofaxialApproaches in the case of Tri- and Tetrasubstituted α-Fluoro Cyclohexanones
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