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- Stereospecific irreversible inhibition of mammalian (S)-ornithine decarboxylase by (R)-(–)-hex-5-yne-1,4-diamine. Patrick Casara, Charles Danzin, Brian W. Metcalf, Michel J. Jung
, J. Chem. Soc., Chem. Commun.
, 1982
, 1190
- Synthetic access to α-substituted prop-2-ynylamines and α-acetylenic amino acids via the t-butyl N-trimethylsilylprop-2-ynylcarbamate dianion. Brian W. Metcalf, Patrick Casara
, J. Chem. Soc., Chem. Commun.
, 1979
, 119
- Enantioselective synthesis of (S)-γ-acetylenic γ-aminobutyric acid (GABA). Andrew B. Holmes, Alethea B. Tabor, Raymond Baker
, J. Chem. Soc., Perkin Trans. 1
, 1991
, 3301
- Chapter 11. Enzyme chemistry. D. Gani
, Annu. Rep. Prog. Chem., Sect. B: Org. Chem.
, 1985
, 82
, 287
- Stereospecific synthesis of (2R,5R)-hept-6-yne-2,5-diamine: a potent and selective enzyme-activated irreversible inhibitor of ornithine decarboxylase (ODC). Patrick Casara, Charles Darwin, Brian Metcalf, Michel Jung
, J. Chem. Soc., Perkin Trans. 1
, 1985
, 2201
- The stereochemical course of decarboxylation, transamination and elimination reactions catalysed by Escherichia coli glutamic acid decarboxylase. Kevin Tilley, Mahmoud Akhtar, David Gani
, J. Chem. Soc., Perkin Trans. 1
, 1994
, 3079
- Enzyme inhibitors in medicine. C. S. J. Walpole, R. Wrigglesworth
, Nat. Prod. Rep.
, 1989
, 6
, 311