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Cited by 320

The DOI matches its Crossref record; 23 of the 23 references it cites were found in a registry or an index.

The chemistry and biological function of natural marine toxins

Yasumoto, Takeshi·2001·The Chemical Record

Abstract

Studies on ciguatera fish poisoning led to clarification of the absolute stereochemistry of ciguatoxin, gambierol, gambieric acids, and maitotoxin. Anisotropic NMR reagents and fluorometric chiral HPLC reagents were effectively used together with synthesis of partial structures. Structures of 16 ciguatoxin congeners were successfully elucidated by FAB/MS/MS using samples of 5 μg or less. Stereochemical assignments were also achieved on dinophysistoxin‐1, pectenotoxins, yessotoxins, polycavernoside‐A, azaspiracid, and prymnesins. The toxins possessed poly‐cyclic‐ether structures and originated from unicellular algae. Biological functions are briefly described. © 2000 John Wiley & Sons, Inc. and The Japan Chemical Journal Forum Chem Rec 1:228–242, 2001

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Metadata

Authors
Yasumoto, T.
Venue
The Chemical Record
Publisher
Wiley
Published
2001-01
Volume
1
Issue
3
Pages
228-242
ISSN
  • 1527-8999 (ISSN-L)
  • 1528-0691
OpenAlex
W2040488025
Cited by
320
References
23
FWCI
7.87
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The chemistry and biological function of natural marine toxins. https://app.cochat.ai/papers/10.1002/tcr.1010
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Yasumoto, T. (2001). The chemistry and biological function of natural marine toxins. The Chemical Record. https://doi.org/10.1002/tcr.1010

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.