Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.


Issue 1, 2017
Previous Article Next Article

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

Author affiliations

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

Back to tab navigation

Supplementary files

Article information


Submitted
25 Oct 2016
Accepted
10 Nov 2016
First published
10 Nov 2016

Org. Biomol. Chem., 2017,15, 65-68
Article type
Communication

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

Social activity

Search articles by author

Spotlight

Advertisements