Stereoselective Synthesis of the C1–C22 Carbon Framework of (−)-Amphidinolide K
Author:
Affiliation:
1. Department of Organic Synthesis & Process Chemistry, Indian Institute of Chemical Technology, Hyderabad 500007, India
2. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India
Funder
Council of Scientific and Industrial Research
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.9b01248
Reference52 articles.
1. aFor reviews on isolation of the amphidinolides, see: Kobayashi, J. In Comprehensive Natural Products Chemistry; Mori, K., Ed. Elsevier: New York, 1999; Vol. 8, p 619.
2. Amphidinolides: Unique Macrolides from Marine Dinoflagellates
3. Amphidinolide K, a new 19-membered macrolide from the cultured symbiotic dinoflagellate Amphidinium sp
4. Amphidinolide H, a novel type of actin-stabilizing agent isolated from dinoflagellate
5. Amphidinolide H, a Potent Cytotoxic Macrolide, Covalently Binds on Actin Subdomain 4 and Stabilizes Actin Filament
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