Efficient Enantioselective Syntheses of (+)-Dalesconol A and B
Author:
Affiliation:
1. State Key Laboratory of Bio-Organic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling Ling Road, Shanghai 200032, China
Funder
China Postdoctoral Science Foundation
National Natural Science Foundation of China
Chinese Academy of Sciences
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
http://pubs.acs.org/doi/pdf/10.1021/jacs.7b00783
Reference31 articles.
1. Unprecedented Immunosuppressive Polyketides fromDaldinia eschscholzii, a Mantis‐Associated Fungus
2. Immunosuppressive Polyketides from Mantis-AssociatedDaldinia eschscholzii
3. Total Synthesis of Cyclosporine: Access to N-Methylated Peptides via Isonitrile Coupling Reactions
4. Naphthol radical couplings determine structural features and enantiomeric excess of dalesconols in Daldinia eschscholzii
5. Three Metabolites from the Mangrove Endophytic Fungus Sporothrix sp. (#4335) from the South China Sea
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