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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. (9th May 2013)
Record Type:
Journal Article
Title:
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. (9th May 2013)
Main Title:
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
<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The crystal structures of 3, 4, 6a, 7, 10, 10a‐hexahydro‐7, 10‐epoxypyrimido[2, 1‐<italic>a</italic>]isoindol‐6(2<italic>H</italic>)‐one, C<sub>11</sub>H<sub>12</sub>N<sub>2</sub>O<sub>2</sub>, and 2‐(2‐aminoethyl)‐3a, 4, 7, 7a‐tetrahydro‐1<italic>H</italic>‐4, 7‐epoxyisoindole‐1, 3(2<italic>H</italic>)‐dione, C<sub>10</sub>H<sub>12</sub>N<sub>2</sub>O<sub>3</sub>, two tricyclic imides, show one and two molecules in the asymmetric unit, respectively. Intermolecular hydrogen‐bonding interactions are observed in both compounds.</p> </abstract>