Accessibility navigation


Syntheses of ethyl 3-deoxy-3,3-difluoro-D-arabino-heptulosonate and analogues

Li, Y., Drew, M.G.B., Welchman, E.V., Shirvastava, R.K., Jiang, S.D., Valentine, R. and Singh, G. (2004) Syntheses of ethyl 3-deoxy-3,3-difluoro-D-arabino-heptulosonate and analogues. Tetrahedron, 60 (31). pp. 6523-6531. ISSN 0040-4020

Full text not archived in this repository.

It is advisable to refer to the publisher's version if you intend to cite from this work. See Guidance on citing.

To link to this item DOI: 10.1016/j.tet.2004.06.048

Abstract/Summary

The difluormated analogues of 3-deoxy-D-arabino-heptulosonic acid (DAH) 12, 24 and its enantiomer have been synthesised from D- and L-crythrose via a Reformatsky reaction which gave a mixture of diastereoiosmers in favour of the anti isomer. (C) 2004 Elsevier Ltd. All rights reserved.

Item Type:Article
Refereed:Yes
Divisions:Faculty of Life Sciences > School of Chemistry, Food and Pharmacy > Department of Chemistry
ID Code:11429
Uncontrolled Keywords:Reformatsky reaction, shikimate pathway, carbohydrate, fluorinated ulosonatm, enzyme inhibitors , SHIKIMATE PATHWAY, APICOMPLEXAN PARASITES, ACID, SYNTHASE, NUCLEOSIDES, DERIVATIVES

University Staff: Request a correction | Centaur Editors: Update this record

Page navigation