Thomas Kurz
Institute of Pharmacy
University of Hamburg
Hamburg
Germany
Name/email consistency: high
- 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)
- 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)
- 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)
- 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)
- 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)
- Efficient conversion of O-substituted 3-hydroxy-4-imino-oxazolidin-2-ones into O-substituted alpha-hydroxyamidoximes. Kurz, T., Widyan, K. Org. Lett. (2004)