Cu-Catalyzed [1,3]-Alkoxy Rearrangement/Diels–Alder Cascade Reactions via in Situ Generation of Functionalized ortho-Quinol Imines
Author:
Affiliation:
1. Research and Analytical Center for Giant Molecules, Graduate School of Science, Tohoku University, Sendai 980-8578 Japan
2. Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan
Funder
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.1c00995
Reference27 articles.
1. Cyclohexadienone Ketals and Quinols: Four Building Blocks Potentially Useful for Enantioselective Synthesis
2. Oxidative Dearomatization of Phenols: Why, How and What For?
3. The ortho-quinol acetates (die ortho-Chinolacetate): 20 years of dedicated research in Vienna and what happened then?
4. Quinol Imides and o-Quinone Imide Diacetates. I. Conversion of 4-Benzenesulfonamidotriphenylmethane to 4-Benzohydryl-o-quinonediacetate-1-benzenesulfonimide
5. Biomimetic Total Synthesis of Bisorbicillinol, Bisorbibutenolide, Trichodimerol, and Designed Analogues of the Bisorbicillinoids
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