Photodimerization of a Pyrido[2,1-a]isoindol-6(4H)-one
Year: 2008
Type: article
Abstract: When subjected to acetone-sensitized irradiation, the title compound undergoes near-quantitative self-coupling to give an uncommon [4+2] dimer, whose reaction with several oxidants demonstrated the enamide double bond of the photoproduct to be the more reactive.
Source: Heterocycles
DOI: 10.3987/com-07-s(n)2
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: diamond
Funder: Ohio State University
OpenAlex ID: W2951764369
