A new synthesis of phosphoramidates: inhibitors of the key bacterial enzyme aspartate semi-aldehyde dehydrogenase

Research output: Contribution to journalArticleResearchpeer review

Authors

  • Luke A. Adams
  • Russell J. Cox
  • Jennifer S. Gibson
  • M. Belén Mayo-Martín
  • Magnus Walter
  • William Whittingham

External Research Organisations

  • University of Bristol
  • Syngenta
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Details

Original languageEnglish
Pages (from-to)2004-2005
Number of pages2
JournalChemical communications
Volume2
Issue number18
Publication statusPublished - 1 Jan 2002
Externally publishedYes

Abstract

A new, mild and high yielding synthesis of phosphoramidates is described: potassium salts of carboxylic acids are treated with ethylchloroformate and the resulting activated anhydride-carbonates are then treated with LiNHP(O)(OEt)2 in situ—the methodology is especially suited to acid sensitive systems featuring BOC,tBu or acetal protecting groups.

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Cite this

A new synthesis of phosphoramidates: inhibitors of the key bacterial enzyme aspartate semi-aldehyde dehydrogenase. / Adams, Luke A.; Cox, Russell J.; Gibson, Jennifer S. et al.
In: Chemical communications, Vol. 2, No. 18, 01.01.2002, p. 2004-2005.

Research output: Contribution to journalArticleResearchpeer review

Adams LA, Cox RJ, Gibson JS, Mayo-Martín MB, Walter M, Whittingham W. A new synthesis of phosphoramidates: inhibitors of the key bacterial enzyme aspartate semi-aldehyde dehydrogenase. Chemical communications. 2002 Jan 1;2(18):2004-2005. doi: 10.1039/b206199f
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