The title compound, C12H24O3, was prepared by the RuO4- catalyzed oxidative cyclization of 2,9-dimethyldeca-2,8-diene. The crystal structure determination has shown unambigously that ring closure produced the trans stereoisomer. Intramolecular O—H O hydrogen bonding generates an S(8) ring motif. Intermolecular O—H O hydrogen bonding leads to the formation of infinite C2 2(4) chains running along the a axis.

rac-2,7-Bis(2-hydroxy-2-propyl)-trans-oxepane / Centore, Roberto; Piccialli, Vincenzo; Tuzi, Angela. - In: ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE. - ISSN 1600-5368. - ELETTRONICO. - E63:(2007), pp. 02907-02908. [10.1107/S1600536807022428]

rac-2,7-Bis(2-hydroxy-2-propyl)-trans-oxepane

CENTORE, ROBERTO;PICCIALLI, VINCENZO;TUZI, ANGELA
2007

Abstract

The title compound, C12H24O3, was prepared by the RuO4- catalyzed oxidative cyclization of 2,9-dimethyldeca-2,8-diene. The crystal structure determination has shown unambigously that ring closure produced the trans stereoisomer. Intramolecular O—H O hydrogen bonding generates an S(8) ring motif. Intermolecular O—H O hydrogen bonding leads to the formation of infinite C2 2(4) chains running along the a axis.
2007
rac-2,7-Bis(2-hydroxy-2-propyl)-trans-oxepane / Centore, Roberto; Piccialli, Vincenzo; Tuzi, Angela. - In: ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE. - ISSN 1600-5368. - ELETTRONICO. - E63:(2007), pp. 02907-02908. [10.1107/S1600536807022428]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/313280
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