Palladium-Catalyzed Double-Decarboxylative Addition to Pyrones: Synthesis of Conjugated Dienoic Esters
Author:
Affiliation:
1. Department of Chemistry, The University of Kansas, 2010 Malott Hall, 1251 Wescoe Hall Drive, Lawrence, Kansas 66045, United States
Funder
Division of Chemistry
Kansas Bioscience Authority
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b02308
Reference48 articles.
1. Total Synthesis of (±)-Cavicularin: Control of Pyrone Diels–Alder Regiochemistry Using Isomeric Vinyl Sulfones
2. Recent advances in diels-alder cycloadditions of 2-pyrones
3. The Mechanism of a Diels-Alder Reaction. I. A Retrodiene Decarboxylation1
4. Total synthesis of (+-)-.alpha.- and (+-)-.beta.-copaenes and ylangenes
5. Enantioselective and Regioselective Pyrone Diels-Alder Reactions of Vinyl Sulfones: Total Synthesis of (+)-Cavicularin
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