2007年12月
Synthesis of the EF-ring of ciguatoxin 3C based on the [2,3]-Wittig rearrangement and ring-closing olefin metathesis
ORGANIC LETTERS
- ,
- ,
- ,
- ,
- 巻
- 9
- 号
- 26
- 開始ページ
- 5373
- 終了ページ
- 5376
- 記述言語
- 英語
- 掲載種別
- 研究論文（学術雑誌）
- DOI
- 10.1021/ol702231j
- 出版者・発行元
- AMER CHEMICAL SOC
The EF-ring segment of ciguatoxin 3C, a causative toxin of ciguatera fish poisoning, was synthesized in three major steps: 1,4-addition for the C20O-C27 bond connection, chirality transferring anti selective [2,3]-Wittig rearrangement for the construction of the anti-2-hydroxyalkyl ether part, and ring-closing olefin metathesis for the F-ring formation.
- リンク情報
-
- DOI
- https://doi.org/10.1021/ol702231j
- CiNii Articles
- http://ci.nii.ac.jp/naid/80018021029
- PubMed
- https://www.ncbi.nlm.nih.gov/pubmed/18052179
- Web of Science
- https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000251614900011&DestApp=WOS_CPL
- ID情報
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- DOI : 10.1021/ol702231j
- ISSN : 1523-7060
- CiNii Articles ID : 80018021029
- PubMed ID : 18052179
- Web of Science ID : WOS:000251614900011