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Gabbutt, Christopher D., Hepworth, John D. and Heron, B. Mark (1992) Enamino ketones as precursors of functionalised 2H-thiopyrans and thiopyrano[2,3-c]- and [3,2-b]-benzothiopyrans. Journal of the Chemical Society, Perkin Transactions 1 (20). pp. 2603-2608. ISSN 0300-922X
Metadata only available from this repository.Official URL: http://dx.doi.org/10.1039/P19920002603
DOI: 10.1039/P19920002603
Abstract
Oxo enamino ketones obtained by treating active methylene compounds with N,N-dimethylformamide dimethyl acetal yield novel 2H-thiopyrans in a regioselective one pot thionation–[4 + 2]-cycloaddition sequence. Application of similar methodology to thiochroman-3-ones affords novel thiopyrano[2,3-c][1]benzothiopyrans and the [3,2-b] isomers.
| Item Type: | Article |
|---|---|
| Subjects: | Q Science > Q Science (General) Q Science > QD Chemistry |
| Schools: | School of Applied Sciences |
| Related URLs: | |
| Depositing User: | Sharon Beastall |
| Date Deposited: | 20 Sep 2012 12:18 |
| Last Modified: | 18 Oct 2012 10:56 |
| URI: | http://eprints.hud.ac.uk/id/eprint/14978 |
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