Synthesis of the C4–C16 Polyketide Fragment of Portimines A and B
Author:
Affiliation:
1. School of Chemical Sciences, The University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand
2. The Maurice Wilkins Centre for Molecular Biodiscovery, The University of Auckland, 3 Symonds Street, Auckland 1010, New Zealand
Funder
Royal Society of New Zealand
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c01463
Reference47 articles.
1. Spiroimine shellfish poisoning (SSP) and the spirolide family of shellfish toxins: Isolation, structure, biological activity and synthesis
2. Cyclic imine toxins from dinoflagellates: a growing family of potent antagonists of the nicotinic acetylcholine receptors
3. Portimine: a bioactive metabolite from the benthic dinoflagellate Vulcanodinium rugosum
4. The Spirocyclic Imine from a Marine Benthic Dinoflagellate, Portimine, Is a Potent Anti-Human Immunodeficiency Virus Type 1 Therapeutic Lead Compound
5. Gymnodimine, a new marine toxin of unprecedented structure isolated from New Zealand oysters and the dinoflagellate, Gymnodinium sp.
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