| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5160572 | Journal of Molecular Structure | 2017 | 6 Pages |
Abstract
A heterocyclic compound commonly known as “indanocyclon” undergoes an unexpected Diels-Alder addition with maleimide. The resulting product has been isolated and characterized in order to get an information about its structure and possible mechanism of the reaction. Extensive comparison of single crystal properties of 3-(2,8-dioxo-1,3-diphenyl-2,8-dihydrocyclopenta[a]inden-8a(1H)-yl)pyrrolidine-2,5-dione and favorable product of the reaction has been also performed.
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Authors
MichaÅ A. Dobrowolski, Piotr Roszkowski, Marta Struga, Daniel Szulczyk,