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
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
1 January 2000
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), .
(doi:10.1016/S0040-4039(99)02031-6).
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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