An Approach towards the Synthesis of the Spiroimine Fragment of 13-Desmethylspirolide C and Gymnodimine A-Reference-Cited by-同舟云学术

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An Approach towards the Synthesis of the Spiroimine Fragment of 13-Desmethylspirolide C and Gymnodimine A

Published:2019-01-02 Issue:6 Volume:25 Page:1553-1560
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Guthertz Alexandre¹,Lusseau Jonathan¹,Desvergnes Valérie¹,Massip Stéphane²,Landais Yannick¹^ORCID

Affiliation:

1. Institute of Molecular Sciences (ISM), UMR-CNRS 5255; University of Bordeaux; 351 Cours de la libération 33405 Talence cedex France

2. European Institute of Chemistry and Biology (IECB); University of Bordeaux; 2 Rue Robert Escarpit 33600 Pessac France

Funder

Agence Nationale de la Recherche

Région Aquitaine

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201804972/fullpdf

Reference90 articles.

1. Spirolides B and D, two novel macrocycles isolated from the digestive glands of shellfish

2. The marine dinoflagellate Alexandrium ostenfeldii (Dinophyceae) as the causative organism of spirolide shellfish toxins

3. Association of the gonyaulacoid dinoflagellate Alexandrium ostenfeldii with spirolide toxins in size-fractionated plankton

4. Characterization of biologically inactive spirolides E and F: Identification of the spirolide pharmacophore

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3. Chiral Lewis Acid-template Diels-Alder Reaction and the Application of Natural Product Synthesis;Journal of Synthetic Organic Chemistry, Japan;2020-03-01

4. Synthetic Studies Towards Spirocyclic Imine Marine Toxins Using N-Acyl Iminium Ions as Dienophiles in Diels–Alder Reactions;Synlett;2020-02-13

5. Reactions of Allylmagnesium Reagents with Carbonyl Compounds and Compounds with C═N Double Bonds: Their Diastereoselectivities Generally Cannot Be Analyzed Using the Felkin–Anh and Chelation-Control Models;Chemical Reviews;2020-01-06

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