Origin of π-Facial Stereoselectivity in Thiophene 1-Oxide Cycloadditions
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States
Funder
Division of Chemistry
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.7b03016
Reference37 articles.
1. Cu-free click cycloaddition reactions in chemical biology
2. Bioorthogonal Cycloadditions: Computational Analysis with the Distortion/Interaction Model and Predictions of Reactivities
3. π-Facial diastereoselectivity in Diels-Alder reactions of 2,5-dimethylthiophene oxide
4. Chemical and Biological Oxidation of Thiophene: Preparation and Complete Characterization of Thiophene S-Oxide Dimers and Evidence for Thiophene S-Oxide as an Intermediate in Thiophene Metabolism in Vivo and in Vitro
5. Lewis Acid Catalysis in the Oxidative Cycloaddition of Thiophenes1
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