6‐β‐(Trifluoromethane sulfonyl)‐amido‐penicillanic acid sulfone

This publication has 14 references indexed in Scilit:

• Penicillanic acid sulfone: an unexpected isotope effect in the interaction of 6.alpha.- and 6.beta.-monodeuterio and of 6,6-dideuterio derivatives with RTEM .beta.-lactamase from Escherichia coli. Crystal structure of penicillanic acid sulfone
  Biochemistry, 1981
• Inactivation of the RTEM .beta.-lactamase from Escherichia coli. Interaction of penam sulfones with the enzyme
  Biochemistry, 1981
• β-Lactamase inactivation by mechanism-based reagents
  Philosophical Transactions of the Royal Society of London. B, Biological Sciences, 1980
• The inhibition of staphylococcal β-lactamase by clavulanic acid
  Biochemical Journal, 1979
• A semi-synthetic penicillinase inactivator
  Nature, 1979
• 6-beta-bromopenicillanic acid, a potent beta-lactamase inhibitor.
  Proceedings of the National Academy of Sciences, 1978
• Kinetic studies on the inactivation of Escherichia coli RTEM β-lactamase by clavulanic acid
  Biochemistry, 1978
• Chapter 25. Bacterial Resistance to β-Lactams: The β-Lactamases
  Published by Elsevier ,1978
• USES OF THE TRIFYL GROUP IN ORGANIC SYNTHESIS. A REVIEW
  Organic Preparations and Procedures International, 1977
• Structural studies on penicillin derivatives. V. Penicillin sulfoxide-sulfenic acid equilibrium
  Journal of the American Chemical Society, 1970