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A biomimetic synthesis of the pyrrolizidine ring by sequential intramolecular cyclizations

A biomimetic synthesis of the pyrrolizidine ring by sequential intramolecular cyclizations
A biomimetic synthesis of the pyrrolizidine ring by sequential intramolecular cyclizations
The pyrrolizidine ring system is generated from an acyclic amide in an acid-catalyzed cyclization in one laboratory operation.
alkaloids
0040-4039
127-129
Marson, C. M.
0ab2b75d-5548-4af8-8d8a-0596d9553a90
Pink, J. H.
89f21204-4214-41b7-9f75-b76728c09ac3
Smith, C.
2019b8d8-ee85-40ff-9bb1-76916a21de6b
Hursthouse, M. B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Malik, K. M. A.
7aaa7d12-fc90-4954-8902-d12e4fbdccdd
Marson, C. M.
0ab2b75d-5548-4af8-8d8a-0596d9553a90
Pink, J. H.
89f21204-4214-41b7-9f75-b76728c09ac3
Smith, C.
2019b8d8-ee85-40ff-9bb1-76916a21de6b
Hursthouse, M. B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Malik, K. M. A.
7aaa7d12-fc90-4954-8902-d12e4fbdccdd

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).

Record type: Article

Abstract

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

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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: 15 Mar 2024 06:10

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Contributors

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

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