Research
19,920 papers- Oxime chemistry in crop protection.Pest management science · 2024
- Non-oxime reactivators of organophosphate-inhibited cholinesterases.Archives of toxicology · 2025
- Oxime Esters: Flexible Building Blocks for Heterocycle Formation.Topics in current chemistry (Cham) · 2023
- A Review of Biologically Active Oxime Ethers.Molecules (Basel, Switzerland) · 2023
- Current approaches to enhancing oxime reactivator delivery into the brain.Toxicology · 2019
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Wikidata facts
Show 3 more facts
- Commons category
- Oximes
- canonical SMILES
- O\N=C(\[*])[*]
- CXSMILES
- O\N=C(\[*])[*] |$;;;R;R$|
Sources (3)
via Wikidata · CC0
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Article
8 sectionsContents
- Structure and properties
- Preparation
- Reactions
- Uses
- Metal extractant
- Other applications
- See also
- References
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In organic chemistry, an oxime is an organic compound belonging to the imines, with the general formula , where R is an organic side-chain and R' may be hydrogen, forming an aldoxime, or another organic group, forming a ketoxime. O-substituted oximes form a closely related family of compounds. Amidoximes are oximes of amides ({{chem2|R^{1}C(\dO)NR^{2}R^{3} }}) with general structure {{chem2|R^{1}C(\dNOH)NR^{2}R^{3} }}.
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