Hydrolytic stability of hydrazones and oximes.
By J. Kalia, Ronald T. Raines. Angewandte Chemie, 2008
786 citations recorded by the source corpus.
Subfields: Molecular Biology, Organic Chemistry
View Paper: https://www.semanticscholar.org/paper/476da996aa435f829daa6ca83bffcdcc7392d9c0
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In Molecular Biology
In Organic Chemistry
Citations in the corpus
- Click Chemistry in Complex Mixtures: Bioorthogonal Bioconjugation (2014, background): “…pH (Kool et al., 2014), it must be remembered that all of these ligations are reversible, and that hydrazones are especially prone to dissociation at low concentrations (Dirksen et al., 2006a; Dirksen et al., 2006b; Kalia and Raines, 2008), whereas oximes are more stable (Kalia and Raines, 2008).”
- Polymer engineering based on reversible covalent chemistry: A promising innovative pathway towards new materials and new functionalities (2018, background): “This is owing to the electron delocalization of oxygen and nitrogen, which greatly improves hydrolytic stability of the corresponding C N bonds [41].”