Berko, Aaron, Horton, Peter N., Hursthouse, Michael B., Packer, Robert J., Went, Michael J. (2005) Synthesis of an alkene functionalised thiamacrocycle, 2,11-divinyl-1,4,7,10,13,16-hexathiacyclooctadeca-2,11-diene. Inorganic Chemistry Communications, 8 (5). pp. 488-490. ISSN 1387-7003. (doi:10.1016/j.inoche.2005.03.003) (KAR id:3765)
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Official URL: http://dx.doi.org/10.1016/j.inoche.2005.03.003 |
Abstract
Base-catalysed rearrangement of 1,4,7-trithiacycloundec-9-yne affords 2,11-Divinyl-1,4,7,10,13,16-hexathiacyclooctadeca-2,11-diene characterised by NMR spectroscopy and X-ray crystallography. The 18-membered macrocycle has six of the 12 C-S bonds in gauche configurations.
Item Type: | Article |
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DOI/Identification number: | 10.1016/j.inoche.2005.03.003 |
Subjects: | Q Science > QD Chemistry |
Divisions: | Divisions > Division of Natural Sciences > Physics and Astronomy |
Depositing User: | Michael Went |
Date Deposited: | 30 Aug 2008 21:15 UTC |
Last Modified: | 05 Nov 2024 09:35 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/3765 (The current URI for this page, for reference purposes) |
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