Asymmetric Synthesis of Double Bond Isomers of the Structure Proposed for Pyrinodemin A and Indication of Its Structural Revision

Asymmetric Synthesis of Double Bond Isomers of the Structure Proposed for Pyrinodemin A and Indication of Its Structural Revision

Asymmetric synthesis of double bond isomers ( )-2 (∆15’,16’) and ( )-3 (∆14’,15’) ofthe structure (1) (∆16’,17’) proposed for pyrinodemin A, a cytotoxic bis-pyridine alkaloidwith a unique cis-cyclopent[c]isoxazolidine moiety from a marine sponge, has been...

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Bibliographic Details
Main Authors: Jun’ichi Kobayashi, Tadashi Endo, Masashi Tsuda, Haruaki Ishiyama
Format: Article
Language:English
Published: MDPI AG 2005-01-01
Series:Molecules
Subjects:
Pyrinodemin A
Amphimedon sp.
asymmetric synthesis
structural revision
Online Access:http://www.mdpi.com/1420-3049/10/1/312/

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http://www.mdpi.com/1420-3049/10/1/312/

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