A general route to protected quaternary ?-amino acids from ?-amino alcohols via a stereocontrolled radical approach

Wood, Mark E., Penny, Mark J., Steere, Jenny S., Horton, Peter N., Light, Mark E. and Hursthouse, Michael B. (2006) A general route to protected quaternary ?-amino acids from ?-amino alcohols via a stereocontrolled radical approach. Chemical Communications, (28), 2983-2985. (doi:10.1039/b604123j).

Record type: Article

Abstract

A radical-based approach facilitates the highly stereocontrolled functionalisation of ?-amino alcohols, opening up a new, generally applicable methodology for the preparation of quaternary ?-amino acids.

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Published date: 2006

Keywords: enantioselective synthesis, functionalization, translocation, alkylation

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Identifiers

Local EPrints ID: 44568

URI: http://eprints.soton.ac.uk/id/eprint/44568

DOI: doi:10.1039/b604123j

ISSN: 1359-7345

PURE UUID: 5444b490-4bb8-49d9-827d-6c20d397f911

ORCID for Peter N. Horton:

orcid.org/0000-0001-8886-2016

ORCID for Mark E. Light:

orcid.org/0000-0002-0585-0843

Catalogue record

Date deposited: 28 Feb 2007

Last modified: 16 Mar 2024 03:12

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Contributors

Author: Mark E. Wood

Author: Mark J. Penny

Author: Jenny S. Steere

Author: Peter N. Horton

Author: Mark E. Light

Author: Michael B. Hursthouse

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