Enantioselective Total Synthesis of (−)-Citrinadin A and Revision of Its Stereochemical Structure
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, The University of Texas, Austin, Texas 78712, United States
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja405547f
Reference49 articles.
1. Citrinadin A, a Novel Pentacyclic Alkaloid from Marine-Derived Fungus Penicillium citrinum
2. Absolute Stereochemistry of Citrinadins A and B from Marine-Derived Fungus
3. PF1270A, B and C, Novel Histamine H3 Receptor Ligands Produced by Penicillium waksmanii PF1270
4. Concise, Stereoselective Approach to the Spirooxindole Ring System of Citrinadin A
5. Tricyclic Alkaloid Core Structures Assembled by a Cyclotrimerization−Coupled Intramolecular Nucleophilic Substitution Reaction
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