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Synthesis of optically pure 4-hydroxymethyl-3-phenoxy-2-azetidinone from D-glucal

Record type: Article

A convenient approach to enantiomerically pure 4-hydroxymethyl- 3-phenoxy-2-azetidinone has been carried out using the easily available aldehyde 5 as chiral starting material.

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Citation

Areces, P., Carrasco, E., Monterde, M., Light, M.E. and Plumet, J. (2007) Synthesis of optically pure 4-hydroxymethyl-3-phenoxy-2-azetidinone from D-glucal Heterocycles, 73, (1), pp. 857-862.

More information

Published date: 2007
Keywords: staudinger reaction, beta-lactam, ozonolysis, beta-lactams, chiral auxiliary, asymmetric-synthesis, carbohydrate

Identifiers

Local EPrints ID: 54237
URI: http://eprints.soton.ac.uk/id/eprint/54237
ISSN: 1881-0942
PURE UUID: 7d9430e4-d810-4b09-9948-76e30382e711
ORCID for M.E. Light: ORCID iD orcid.org/0000-0002-0585-0843

Catalogue record

Date deposited: 31 Jul 2008
Last modified: 17 Jul 2017 14:36

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Contributors

Author: P. Areces
Author: E. Carrasco
Author: M. Monterde
Author: M.E. Light ORCID iD
Author: J. Plumet

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