A Comparison Of 3,4,6A,7,10,10A-Hexahydro-7,10-Epoxypyrimido 2,1-A Isoindol-6(2H)-One And 2-(2-Aminoethyl)-3A,4,7,7A-Tetrahydro-1H-4,7-Epoxyisoindole-1,3(2H)-Dion E: Structural And Reactivity Differences Of Two Homologous Tricyclic Imides

Date

2013-06

Authors

Mitchell, Lauren A.
Stanley, Julie M.
De Hoyos, Liliana Espinosa
Holliday, Bradley J.

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Abstract

The crystal structures of 3,4,6a,7,10,10a-hexahydro-7,10-epoxypyrimido[2,1-a]isoindol-6(2H)-one, C11H12N2O2, and 2-(2-aminoethyl)-3a,4,7,7a-tetrahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione, C10H12N2O3, two tricyclic imides, show one and two molecules in the asymmetric unit, respectively. Intermolecular hydrogen-bonding interactions are observed in both compounds.

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Citation

Mitchell, Lauren A., Stanley, Julie M., De Hoyos, Liliana Espinosa, Holliday, Bradley J., >A comparison of 3,4,6a,7,10,10a-hexahydro-7,10-epoxypyrimido[2,1-a]isoindol-6(2H)-one and 2-(2-aminoethyl)-3a,4,7,7a-tetrahydro-1H-4,7-epoxyisoindole-1,3(2H)-dione: structural and reactivity differences of two homologous tricyclic imides,> Acta Crystallogr C. 2013 Jun;69(Pt 6):638-41. doi: 10.1107/S0108270113010706. Epub 2013 May 2. doi: 10.1107/S0108270113010706