Efficient Total Synthesis of Marine Alkaloid (-)-NakadomarinA
Z's top: For the total synthesis of the marine alkaloid (-)-nakadomarinA, (-)-camphorsulfonic acid assisted, Z-selective, olefin RCM of a monoamine (less polar) rather than a diamine (more polar) was found to be highly practical for constructing the Fring. The ABCD-tetracyclic core was assemble...
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Veröffentlicht in: | Chemistry : a European journal 2011-11, Vol.17 (45), p.12569-12572 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Z's top: For the total synthesis of the marine alkaloid (-)-nakadomarinA, (-)-camphorsulfonic acid assisted, Z-selective, olefin RCM of a monoamine (less polar) rather than a diamine (more polar) was found to be highly practical for constructing the Fring. The ABCD-tetracyclic core was assembled through a novel efficacious PtCl sub(2)-promoted cascade reaction sequence (see scheme). |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.201102101 |