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Updated: Feb 24, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Metastable Intermediates (Isoindenes, Isofluorenes, and Isobenzofurans) from Alkyne Precursors via Free Carbenes
Jackson C Orr1, Thomas R Hoye1
1Department of Chemistry, University of Minnesota, 207 Pleasant Street, SE, Minneapolis, Minnesota 55455, United States.
Abstract:
We report here reactions between a free carbene center and a suitably appended π-bond (C═X) that give rise to reactive intermediates that, in turn, undergo various types of additional transformations (cycloadditions, rearrangements, and ring openings). Participation of the following C═X functional groups is demonstrated: alkene, arene, heteroarene, aldehyde, ester, ketone, amide, and carbamate. The overall transformations are thermally driven and often produce no byproducts. Each is initiated by the generation of a carbene that is fueled by the potential energy provided by two complementary alkyne coreactants.
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