Issue 8, 2014

Enyne [4 + 4] photocycloaddition with polycyclic aromatics

Abstract

Polycyclic aromatics undergo [4 + 4] photocycloaddition to give substituted cyclooctadiene products. We have examined the [4 + 4] photoreactivity of these aromatics with enynes using a recently developed substitution pattern that undergoes a 1,3-hydrogen migration, forming a single cycloadduct. Several substrates yield stable, isomerized [4 + 4] adducts.

Graphical abstract: Enyne [4 + 4] photocycloaddition with polycyclic aromatics

Associated articles

Supplementary files

Article information

Article type
Research Article
Submitted
07 jul 2014
Accepted
29 jul 2014
First published
31 jul 2014

Org. Chem. Front., 2014,1, 961-964

Author version available

Enyne [4 + 4] photocycloaddition with polycyclic aromatics

B. B. Khatri, S. Kulyk and S. McN. Sieburth, Org. Chem. Front., 2014, 1, 961 DOI: 10.1039/C4QO00190G

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