A Stereoconvergent Intramolecular Diels–Alder Cycloaddition Related to the Construction of the Decalin Core of neo-Clerodane Diterpenoids
Author:
Affiliation:
1. Department of Chemistry, The University of Texas at Tyler, Tyler, Texas 75799, United States
2. Department of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio 43210, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo400029u
Reference22 articles.
1. Synthesis of Clerodane Diterpenoids and Related Compounds - Stereoselective Construction of the Decalin Skeleton with Multiple Contiguous Stereogenic Centers
2. Salvinorin A Analogs as Probes in Opioid Pharmacology
3. Salvinorin A: A potent naturally occurring nonnitrogenous opioid selective agonist
4. Identification of the Molecular Mechanisms by Which the Diterpenoid Salvinorin A Binds to κ-Opioid Receptors
5. Salvinorin, a new trans-neoclerodane diterpene from Salvia divinorum(Labiatae)
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