Enantioselective Synthesis of γ-Aryl-γ-butyrolactones by Sequential Asymmetric Epoxidation, Ring Expansion, and Baeyer−Villiger Oxidation
Author:
Affiliation:
1. Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523 yian@lamar.colostate.edu
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo061341j
Reference18 articles.
1. Lipase-catalyzed preparation of optically active .gamma.-butyrolactones in organic solvents
2. Novel Method for the Synthesis of Chiral 4-Aryl-γ-butyrolactones via Cascade Asymmetric Epoxidation—Ring Expansion—Baeyer-Villiger Reaction of Cyclopropylidene Derivatives
3. Asymmetric total synthesis of (+)-equilenin utilizing two types of cascade ring expansion reactions of small ring systems
4. New synthetic reactions. Secoalkylation
5. A concise and enantioselective approach to cyclobutanones by tandem asymmetric epoxidation and enantiospecific ring expansion of cyclopropylidene alcohols. An enantiocontrolled synthesis of (+)- and (-)-.alpha.-cuparenones
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