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Structural transformations in zopiclone

Shankland, N. and David, W.I.F. and Shankland, K. and Kennedy, A.R. and Frampton, C.S. and Florence, A.J. (2001) Structural transformations in zopiclone. Chemical Communications (London), 2001 (21). pp. 2204-2205. ISSN 0009-241X

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Abstract

A monoclinic centrosymmetric form of zopiclone dihydrate undergoes a sequential, two-step transformation in the solid-state upon heating which results in separation of the enantiomers into a racemic conglomerate or racemic twins.

Item type: Article
ID code: 1180
Keywords: monoclinic, centrosymmetric form, zopiclone dihydrate, heating, racemic conglomerate, racemic twins, Chemistry
Subjects: Science > Chemistry
Department: Faculty of Science > Pure and Applied Chemistry
Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences > Pharmaceutical Sciences
Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences
Related URLs:
    Depositing user: Catriona Mccallum
    Date Deposited: 26 May 2006
    Last modified: 04 Oct 2012 15:22
    URI: http://strathprints.strath.ac.uk/id/eprint/1180

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