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A biomimetic synthesis of the pyrrolizidine ring by sequential intramolecular cyclizations

Record type: Article

The pyrrolizidine ring system is generated from an acyclic amide in an acid-catalyzed cyclization in one laboratory operation.

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Citation

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), pp. 127-129. (doi:10.1016/S0040-4039(99)02031-6).

More information

Published date: 1 January 2000
Keywords: alkaloids

Identifiers

Local EPrints ID: 19069
URI: http://eprints.soton.ac.uk/id/eprint/19069
ISSN: 0040-4039
PURE UUID: fd934e95-851c-4e47-b6bc-e6dedd64da6c

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Date deposited: 15 Dec 2005
Last modified: 17 Jul 2017 16:33

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Contributors

Author: C. M. Marson
Author: J. H. Pink
Author: C. Smith
Author: M. B. Hursthouse
Author: K. M. A. Malik

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