Increasing the Efficiency of the Transannular Diels–Alder Strategy via Palladium(II)-Catalyzed Macrocyclizations
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095-1569, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol303394t
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4. Exploration of a proposed biomimetic synthetic route to plumarellide. Development of a facile transannular Diels–Alder reaction from a macrocyclic enedione leading to a new 5,6,7-tricyclic ring system
5. Total Synthesis of (+)-Superstolide A
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