A biomimetic synthesis of the pyrrolizidine ring by sequential intramolecular cyclizations
Marson, C. M., Pink, J. H., Smith, C., Hursthouse, M. B. and Malik, K. M. A. (2000) A biomimetic synthesis of the pyrrolizidine ring by sequential intramolecular cyclizations. Tetrahedron Letters, 41, (1), 127-129. (doi:10.1016/S0040-4039(99)02031-6)
Download
Full text not available from this repository.
Official URL: http://dx.doi.org/10.1016/S0040-4039(99)02031-6
Description/Abstract
The pyrrolizidine ring system is generated from an acyclic amide in an acid-catalyzed cyclization in one laboratory operation.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | alkaloids |
| Related URLs: | http://dx.doi.org/10.1016/S004...99)02031-6 |
| Subjects: | Q Science Q Science > QD Chemistry |
| Divisions: | University Structure - Pre August 2011 > School of Chemistry |
| ePrint ID: | 19069 |
| URI: | http://eprints.soton.ac.uk/id/eprint/19069 |
| Deposited On: | 15 Dec 2005 |
| Last Modified: | 01 Jun 2011 12:01 |
Associated Staff Only: edit my ePrint

