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A novel route towards formylated 1,3-dithiole-2-thiones via an unprecedented allylic 1,4-diol rearrangement

Record type: Article

In the presence of perchloric acid, an unusual 1,4-aryl shift is observed for two electron-rich 4,5-bis[hydroxy(aryl)methyl]-1,3-dithiole-2-thiones; the X-ray crystal structure of compound 8 confirms the structural identity of the rearrangement product.

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Citation

Khan, T., Skabara, P. J., Coles, S. J. and Hursthouse, M. B. (2001) A novel route towards formylated 1,3-dithiole-2-thiones via an unprecedented allylic 1,4-diol rearrangement Chemical Communications, (4), pp. 369-370. (doi:10.1039/b009550h).

More information

Published date: 2001
Keywords: chemistry

Identifiers

Local EPrints ID: 19531
URI: http://eprints.soton.ac.uk/id/eprint/19531
ISSN: 1359-7345
PURE UUID: 0acaff2e-65a1-4cd7-afcb-caff99b0e3a2
ORCID for S. J. Coles: ORCID iD orcid.org/0000-0001-8414-9272

Catalogue record

Date deposited: 14 Feb 2006
Last modified: 17 Jul 2017 16:31

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Contributors

Author: T. Khan
Author: P. J. Skabara
Author: S. J. Coles ORCID iD

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