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Gabbutt, Christopher D., Hepworth, John D., Heron, B. Mark and Pugh, Samantha L. (2002) A facile route to pyrroles, isoindoles and hetero fused analogues. Journal of the Chemical Society, Perkin Transactions 1 (24). pp. 2799-2808. ISSN 1472-7781
Metadata only available from this repository.Official URL: http://dx.doi.org/10.1039/B209255G
DOI: 10.1039/B209255G
Abstract
Enamino acids derived from 1,2-dimethylaminomethylene- or 1,2-hydroxymethylene-carbonyl compounds and amino acids undergo a decarboxylative cyclisation to pyrroles, isoindoles and other fused pyrroles. A two atom ring expansion occurs preferentially with enamino acids from cyclohexane-1,3-diones and α-alkyl-α-amino acids leading to oxocino[2,3-c]pyrroles.
| 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: | 25 Sep 2012 10:39 |
| Last Modified: | 18 Oct 2012 09:50 |
| URI: | http://eprints.hud.ac.uk/id/eprint/15044 |
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