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Pivampicillin

Known as: Ester, Ampicillin Pivaloyl, Pivampicillinum, Pivaloylampicillin 
A semisynthetic, orally active pivalate ester of ampicillin with antibacterial activity. Upon absorption, pivampicillin is hydrolyzed into its active… 
National Institutes of Health

Papers overview

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Review
2017
Review
2017
N-Tosylhydrazones have recently emerged as useful synthons in a variety of transition-metal-catalyzed and transition-metal-free… 
Highly Cited
2014
Highly Cited
2014
  • J. NeelyT. Rovis
  • Journal of the American Chemical Society
  • 2014
  • Corpus ID: 12249429
α,β-Unsaturated carboxylic acids undergo Rh(III)-catalyzed decarboxylative coupling with α,β-unsaturated O-pivaloyl oximes to… 
Highly Cited
2013
Highly Cited
2013
  • J. NeelyT. Rovis
  • Journal of the American Chemical Society
  • 2013
  • Corpus ID: 207091197
α,β-Unsaturated O-pivaloyl oximes are coupled to alkenes by Rh(III) catalysis to afford substituted pyridines. The reaction with… 
Highly Cited
2001
Highly Cited
2001
Homo oligomers of (1-->2)-beta-D-mannopyranosyl residues have been synthesized in order to study the unique immunological… 
Highly Cited
1992
Highly Cited
1992
The pharmacokinetics of ampicillin and amoxicillin following intravenous administration at a dose rate of 15 and 10 mg/kg… 
Highly Cited
1986
Highly Cited
1986
Highly Cited
1981
Highly Cited
1978
Highly Cited
1978
Bacampicillin, a new oral prodrug which in vivo is rapidly transformed to ampicillin, was compared with ampicillin, pivampicillin…