Cited by 29Chemical Reaction MechanismsSynthesis of β-Lactam CompoundsAdvanced Synthetic Organic Chemistry

Studies on the hydrolysis of clavulanic acid

Finn, Malcolm J., Harris, Michael A., Hunt, Eric, Zomaya, Iskander I.·1984·Journal of the Chemical Society, Perkin Transactions 1

Abstract

1-Amino-4-hydroxybutan-2-one (14) has been identified as one of the major products from the hydrolysis of clavulanic acid in acidic, alkaline, or neutral solution. In alkaline or neutral solution, the amino ketone (14) is converted into other products, including two pyrazines, 2,5-bis(2-hydroxyethyl)pyrazine and 3-ethyl-2,5-bis(2-hydroxyethyl)pyrazine. A rationale for the formation of these products is discussed.

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Crossref · 10.1039/p19840001345

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  • The kinetic approach is consequent with a feasible chemical mechanism of reaction for CA in aqueous solutions characterized by several equilibrium steps.

    “This kinetic approach is consequent with a feasible chemical mechanism of reaction for CA in aqueous solutions, characterized by several equilibrium steps (Figure 4) [28,29].”

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Authors
Finn, M. J., Harris, M. A., Hunt, E., & Zomaya, I. I.
Venue
Journal of the Chemical Society, Perkin Transactions 1
Published
1984
Pages
1345
ISSN
  • 1364-5463 (ISSN-L)
  • 0300-922X
OpenAlex
W2160354525
Cited by
29
References
0
Citations by year
2026: 1 · 2024: 1 · 2022: 2 · 2020: 1 · 2019: 2 · 2018: 1 · 2015: 4 · 2014: 1 · 2013: 2 · 2012: 1
FWCI
0.56
Type
journal article
Language
en
Open access
closed
Locations
Journal of the Chemical Society Perkin Transactions 1 (publishedVersion)
Funders
University of Minnesota
Topics
  • Physical Sciences › Chemistry › Organic Chemistry › Chemical Reaction Mechanisms
  • Physical Sciences › Chemistry › Organic Chemistry › Synthesis of β-Lactam Compounds
  • Physical Sciences › Chemistry › Organic Chemistry › Advanced Synthetic Organic Chemistry
Keywords
clavulanic acid, hydrolysis, amino ketones, pyrazine, alkaline hydrolysis, acid hydrolysis, neutral hydrolysis, degradation products

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