Lewis acid mediated cyclisations of silylated methylenecyclopropyl hydrazones
Lewis acid mediated cyclisations of silylated methylenecyclopropyl hydrazones
Silylated methylenecyclopropyl hydrazones on treatment with BF3.Et2O cyclise to give heterocyclic products involving a novel sequence of hydride and silyl shifts via a series of increasingly stable cationic intermediates.
cycloaddition, aldehydes, acylhydrazones, additions, ketones
2552-2553
Patient, L.
ce95f606-faf0-477e-9129-ed2b85bb9c6c
Berry, M. B.
8a21d139-9bf7-45a4-a32e-be4a4b3282b5
Coles, S. J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Hursthouse, M. B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Kilburn, J. D.
c02957da-baca-4138-961a-a85170d11dd8
2003
Patient, L.
ce95f606-faf0-477e-9129-ed2b85bb9c6c
Berry, M. B.
8a21d139-9bf7-45a4-a32e-be4a4b3282b5
Coles, S. J.
3116f58b-c30c-48cf-bdd5-397d1c1fecf8
Hursthouse, M. B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Kilburn, J. D.
c02957da-baca-4138-961a-a85170d11dd8
Patient, L., Berry, M. B., Coles, S. J., Hursthouse, M. B. and Kilburn, J. D.
(2003)
Lewis acid mediated cyclisations of silylated methylenecyclopropyl hydrazones.
Chemical Communications, (20), .
(doi:10.1039/b306636c).
Abstract
Silylated methylenecyclopropyl hydrazones on treatment with BF3.Et2O cyclise to give heterocyclic products involving a novel sequence of hydride and silyl shifts via a series of increasingly stable cationic intermediates.
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Published date: 2003
Keywords:
cycloaddition, aldehydes, acylhydrazones, additions, ketones
Identifiers
Local EPrints ID: 20059
URI: http://eprints.soton.ac.uk/id/eprint/20059
ISSN: 1359-7345
PURE UUID: ce6e0da8-2f15-48e5-bb9b-6f0661c8f40e
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Date deposited: 22 Feb 2006
Last modified: 16 Mar 2024 03:05
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Author:
L. Patient
Author:
M. B. Berry
Author:
J. D. Kilburn
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