Total Synthesis of Bioactive Natural Products by Palladium-Catalyzed Domino Cyclization of Allenes and Related Compounds

The author has developed novel methodologies for highly efficient construction of functionalized heterocycles by palladium-catalyzed domino/cascade cyclization of allenes and related compounds containing appropriate nucleophilic group(s). Based on these methodologies, enantioselective total synthese...

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Bibliografiske detaljer
Hovedforfatter: Inuki, Shinsuke
Format: Livre numérique
Sprog:Anglais
Udgivet: Tokyo : Springer Japan [20..].
Cham : Springer Nature
Udgivelse:1st ed. 2012.
Serier:Springer Theses, Recognizing Outstanding Ph.D. Research
Online adgang:Accès sur la plateforme de l'éditeur
Accès sur la plateforme Istex
Accès Université d'Orléans
Accès INSA CVL
Kommentar: Archives Springer e-books (Licence nationale)
Archives Springer e-books (Licence nationale)
Autres localisations: Voir dans le Sudoc
Edition sous un autre format:• Total Synthesis of Bioactive Natural Products by Palladium-Catalyzed Domino Cyclization of Allenes and Related Compounds, Texte imprimé, 9784431540427
• Total Synthesis of Bioactive Natural Products by Palladium-Catalyzed Domino Cyclization of Allenes and Related Compounds, Texte imprimé, 9784431540441
• Total Synthesis of Bioactive Natural Products by Palladium-Catalyzed Domino Cyclization of Allenes and Related Compounds, Texte imprimé, 9784431561101
• Total Synthesis of Bioactive Natural Products by Palladium-Catalyzed Domino Cyclization of Allenes and Related Compounds, Texte imprimé, 9784431540427
• Total Synthesis of Bioactive Natural Products by Palladium-Catalyzed Domino Cyclization of Allenes and Related Compounds, Texte imprimé, 9784431540441
• Total Synthesis of Bioactive Natural Products by Palladium-Catalyzed Domino Cyclization of Allenes and Related Compounds, Texte imprimé, 9784431561101
Indholdsfortegnelse:
  • Chapter 1. Total Synthesis of Pachastrissamine (Jaspine B) Chapter 2. Total Synthesis of Lysergic Acid, Lysergol, and Isolysergol Chapter 3. Conclusions.