Synthesis, Structure, and Reactivity of Unexpectedly Stable Spiroepoxy-β-Lactones Obtained by Epoxidation of 4-Alkylidene-2-Oxetanones
Author:
Affiliation:
1. Department of Chemistry, Texas A&M University, P.O. Box 30012, College Station, Texas 77842-3012
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja053478h
Reference13 articles.
1. Recent Advances in β-Lactone Chemistry
2. Methods for the synthesis of optically active β-lactones (2-oxetanones)
3. β-Lactones: Intermediates for Natural Product Total Synthesis and New Transformations
4. Asymmetric Synthesis of Highly Substituted ?-Lactones by Nucleophile-Catalyzed [2+2] Cycloadditions of Disubstituted Ketenes with Aldehydes
5. Catalytic, Asymmetric Preparation of Ketene Dimers from Acid Chlorides
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