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Thomas Kurz

Institute of Pharmacy

University of Hamburg

Hamburg

Germany

[email]@*.uni-hamburg.de

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Institute of Pharmacy, University of Hamburg, Hamburg, Germany. 2004 - 2007

References

  1. gamma-Substituted bis(pivaloyloxymethyl)ester analogues of fosmidomycin and FR900098. Kurz, T., Behrendt, C., Pein, M., Kaula, U., Bergmann, B., Walter, R.D. Arch. Pharm. (Weinheim) (2007) [Pubmed]
  2. Conformationally restrained aromatic analogues of fosmidomycin and FR900098. Kurz, T., Schlüter, K., Pein, M., Behrendt, C., Bergmann, B., Walter, R.D. Arch. Pharm. (Weinheim) (2007) [Pubmed]
  3. Synthesis and antimalarial activity of chain substituted pivaloyloxymethyl ester analogues of Fosmidomycin and FR900098. Kurz, T., Schlüter, K., Kaula, U., Bergmann, B., Walter, R.D., Geffken, D. Bioorg. Med. Chem. (2006) [Pubmed]
  4. Conventional and microwave-assisted conversion of substituted 3-amino-oxazolidin-2,4-diones into N',N'-disubstituted alpha-hydroxyhydrazides. Kurz, T., Widyan, K. J. Org. Chem. (2005) [Pubmed]
  5. O-Protected 3-hydroxy-oxazolidin-2,4-diones: novel precursors in the synthesis of alpha-hydroxyhydroxamic acids. Kurz, T., Widyan, K. Org. Biomol. Chem. (2004) [Pubmed]
  6. Efficient conversion of O-substituted 3-hydroxy-4-imino-oxazolidin-2-ones into O-substituted alpha-hydroxyamidoximes. Kurz, T., Widyan, K. Org. Lett. (2004) [Pubmed]
 
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