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...

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Veröffentlicht in:Organic & biomolecular chemistry 2017, Vol.15 (1), p.65-68
Hauptverfasser: Dethe, Dattatraya H, Dherange, Balu D, Ali, Saghir, Parsutkar, Mahesh M
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container_title Organic & biomolecular chemistry
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creator Dethe, Dattatraya H
Dherange, Balu D
Ali, Saghir
Parsutkar, Mahesh M
description 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.
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title Enantiospecific total syntheses of meroterpenoids (-)-F1839-I and (-)-corallidictyals B and D
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