Syntheses of (−)-Funebrine and (−)-Funebral, Using Sequential Transesterification and Intramolecular Cycloaddition of a Chiral Nitrone
Author:
Affiliation:
1. Faculty of Pharmaceutical Sciences, Kanazawa University, Takara-machi, Kanazawa 920-0934, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo030257q
Reference23 articles.
1. Funebrine, a structurally novel pyrrole alkaloid, and other .gamma.-hydroxyisoleucine-related metabolites of Quararibea funebris (Llave) Vischer (Bombacaceae)
2. Funebral, a New Pyrrole Lactone Alkaloid from Quararibea funebris
3. Quararibea Metabolites. 4.1 Total Synthesis and Conformational Studies of (±)-Funebrine and (±)-Funebral
4. Stereoselective synthesis of the dihydroxyisoleucine constituent of the amanita mushroom toxins
5. Ester-enolate Claisen rearrangement of .alpha.-amino acid derivatives
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