Enantiospecific total syntheses of meroterpenoids (-)-F1839-I and (-)-corallidictyals B and D

Enantiospecific total syntheses of meroterpenoids (-)-F1839-I and (-)-corallidictyals B and D

Enantiospecific total syntheses of spiromeroterpenoid natural products (-)-F1839-I and (-)-corallidictyals B and D were achieved using the environmentally benign and highly atom economical Lewis acid catalysed Friedel-Crafts reaction and a highly regio- and stereoselective spirocyclic C-O bond forma...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Organic & biomolecular chemistry 2017, Vol.15 (1), p.65-68
Hauptverfasser: Dethe, Dattatraya H, Dherange, Balu D, Ali, Saghir, Parsutkar, Mahesh M
Format: Artikel
Sprache:eng
Schlagworte:
Biological Products - chemical synthesis
Biological Products - chemistry
Catalysis
Green Chemistry Technology
Lewis Acids - chemistry
Models, Molecular
Sesquiterpenes - chemical synthesis
Sesquiterpenes - chemistry
Stereoisomerism
Terpenes - chemical synthesis
Terpenes - chemistry
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Enantiospecific total syntheses of spiromeroterpenoid natural products (-)-F1839-I and (-)-corallidictyals B and D were achieved using the environmentally benign and highly atom economical Lewis acid catalysed Friedel-Crafts reaction and a highly regio- and stereoselective spirocyclic C-O bond formation reaction.
ISSN:1477-0520
1477-0539
DOI:10.1039/c6ob02322c