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Lewis acid-mediated addition of silylated methylenecyclopropane to aldehydes - synthesis of tetrahydrofuran derivatives

Lewis acid-mediated addition of silylated methylenecyclopropane to aldehydes - synthesis of tetrahydrofuran derivatives
Lewis acid-mediated addition of silylated methylenecyclopropane to aldehydes - synthesis of tetrahydrofuran derivatives
Lewis acid-mediated intermolecular addition of silylated methylenecyclopropane to aldehydes provides a novel route to tetrahydrofuran derivatives.
methylenecyclopropane, lewis acid, tetrahydrofuran cascade radical cyclizations, catalyzed 3+2 cycloadditions, palladium, ketones
0040-4039
1015-1017
Patient, L.
ce95f606-faf0-477e-9129-ed2b85bb9c6c
Berry, M. B.
8a21d139-9bf7-45a4-a32e-be4a4b3282b5
Kilburn, J. D.
c02957da-baca-4138-961a-a85170d11dd8
Patient, L.
ce95f606-faf0-477e-9129-ed2b85bb9c6c
Berry, M. B.
8a21d139-9bf7-45a4-a32e-be4a4b3282b5
Kilburn, J. D.
c02957da-baca-4138-961a-a85170d11dd8

Patient, L., Berry, M. B. and Kilburn, J. D. (2003) Lewis acid-mediated addition of silylated methylenecyclopropane to aldehydes - synthesis of tetrahydrofuran derivatives. Tetrahedron Letters, 44 (5), 1015-1017. (doi:10.1016/S0040-4039(02)02888-5).

Record type: Article

Abstract

Lewis acid-mediated intermolecular addition of silylated methylenecyclopropane to aldehydes provides a novel route to tetrahydrofuran derivatives.

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More information

Published date: 27 January 2003
Keywords: methylenecyclopropane, lewis acid, tetrahydrofuran cascade radical cyclizations, catalyzed 3+2 cycloadditions, palladium, ketones
Organisations: Chemistry

Identifiers

Local EPrints ID: 20060
URI: http://eprints.soton.ac.uk/id/eprint/20060
ISSN: 0040-4039
PURE UUID: fab2a9b4-c3b2-4ecb-a0be-e89cac648b84

Catalogue record

Date deposited: 20 Feb 2006
Last modified: 15 Mar 2024 06:21

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Contributors

Author: L. Patient
Author: M. B. Berry
Author: J. D. Kilburn

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