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Lewis acid mediated endo-cyclisation of trimethylsilylmethylenecyclopropyl imines - a stereoselective route to indolizidines

Lewis acid mediated endo-cyclisation of trimethylsilylmethylenecyclopropyl imines - a stereoselective route to indolizidines
Lewis acid mediated endo-cyclisation of trimethylsilylmethylenecyclopropyl imines - a stereoselective route to indolizidines
Lewis acid mediated endo-cyclisation of trimethylsilylmethylenecyclopropyl imines provides a stereoselective route to indolizidines via a novel cascade sequence.
mgi2-mediated ring expansions, methylenecyclopropyl ketones, opening reactions, aldehydes, alkylidenecyclopropanes, cycloaddition, derivatives, selectivity, palladium, amides
1359-7345
1637-1639
Rajamaki, Suvi
0b36ed69-c201-4bbe-b037-b80925082e8d
Kilburn, Jeremy D.
e64ded70-825a-40ec-816b-c4605e007e7a
Rajamaki, Suvi
0b36ed69-c201-4bbe-b037-b80925082e8d
Kilburn, Jeremy D.
e64ded70-825a-40ec-816b-c4605e007e7a

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).

Record type: 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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More information

Published date: 2005
Additional Information: ChemComm
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
ISSN: 1359-7345
PURE UUID: db506d14-78a5-4874-8a76-e60662a35785

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Date deposited: 02 Mar 2006
Last modified: 15 Jul 2019 19:25

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Contributors

Author: Suvi Rajamaki
Author: Jeremy D. Kilburn

University divisions

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