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).
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Original Publication 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 |
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| Related URLs: | |
| Keywords: | alkaloids |
| Subjects: | Q Science Q Science > QD Chemistry |
| Divisions: | University Structure - Pre August 2011 > School of Chemistry |
| Item ID: | 19069 |
| Date Deposited: | 15 Dec 2005 |
| Last Modified: | 01 Jun 2011 11:01 |
| Contributors: | Marson, C. M. (Author) Pink, J. H. (Author) Smith, C. (Author) Hursthouse, M. B. (Author) Malik, K. M. A. (Author) |
| Date: | 1 January 2000 |
| Status: | Published |
| URI: | http://eprints.soton.ac.uk/id/eprint/19069 |
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