Rajamaki, Suvi and Kilburn, Jeremy D. (2005) Lewis acid mediated endo-cyclisation of trimethylsilylmethylenecyclopropyl imines - a stereoselective route to indolizidines. Chemical Communications, 2005 (12), 1637-1639. (doi:10.1039/b418476a).
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Article
Abstract
Lewis acid mediated endo-cyclisation of trimethylsilylmethylenecyclopropyl imines provides a stereoselective route to indolizidines via a novel cascade sequence.
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Published date: 2005
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ChemComm
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Keywords:
mgi2-mediated ring expansions, methylenecyclopropyl ketones, opening reactions, aldehydes, alkylidenecyclopropanes, cycloaddition, derivatives, selectivity, palladium, amides
Identifiers
Local EPrints ID: 20893
URI: http://eprints.soton.ac.uk/id/eprint/20893
DOI: doi:10.1039/b418476a
ISSN: 1359-7345
PURE UUID: db506d14-78a5-4874-8a76-e60662a35785
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Date deposited: 02 Mar 2006
Last modified: 15 Mar 2024 06:26
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Contributors
Author:
Suvi Rajamaki
Author:
Jeremy D. Kilburn
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