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Issue 1, 2017
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Enantiospecific total syntheses of meroterpenoids (−)-F1839-I and (−)-corallidictyals B and D

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Abstract

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.

Graphical abstract: Enantiospecific total syntheses of meroterpenoids (−)-F1839-I and (−)-corallidictyals B and D

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Publication details

The article was received on 25 Oct 2016, accepted on 10 Nov 2016 and first published on 10 Nov 2016


Article type: Communication
DOI: 10.1039/C6OB02322C
Citation: Org. Biomol. Chem., 2017,15, 65-68
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    Enantiospecific total syntheses of meroterpenoids (−)-F1839-I and (−)-corallidictyals B and D

    D. H. Dethe, B. D. Dherange, S. Ali and M. M. Parsutkar, Org. Biomol. Chem., 2017, 15, 65
    DOI: 10.1039/C6OB02322C

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