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ester
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130px|thumb|An ester of a carboxylic acid. R stands for [[hydrogen, halogen or organyl and R stands for any organyl group.]] In chemistry, an ester is a compound derived from an acid (either organic or inorganic) in which the hydrogen atom (H) of at least one acidic hydroxyl group () of that acid is replaced by an organyl group (R). These compounds contain a distinctive functional group. Analogues derived from oxygen replaced by other chalcogens belong to the ester category as well. According to some authors, organyl derivatives of acidic hydrogen of other acids are esters as well (e.g. amides
An ester is a chemical compound formed when the hydrogen atom in an acid is replaced by an organic group, creating a molecule with a distinctive structure. Esters are important because they occur widely in nature and industry—for example, they make up fats and oils, and they're used in fragrances, plastics, and many other everyday products.
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Research
212,849 papers- Enzymatic ester bond formation strategies in fungal macrolide skeletons.ReviewNatural product reports · 2025Zhang JM, Yuan GY, Zou YDOI: 10.1039/d4np00050a
- Preserving ester-linked modifications reveals glutamate and aspartate mono-ADP-ribosylation by PARP1 and its reversal by PARG.Nature communications · 2024Longarini EJ, Matić IDOI: 10.1038/s41467-024-48314-0
- Carboxylic ester hydrolases from hyperthermophiles.ReviewExtremophiles : life under extreme conditions · 2009Levisson M, van der Oost J, Kengen SWDOI: 10.1007/s00792-009-0260-4
- Microbial esterases and ester prodrugs: An unlikely marriage for combating antibiotic resistance.ReviewDrug development research · 2019Larsen EM, Johnson RJDOI: 10.1002/ddr.21468
- [Evaluation of the Oral Absorption of Ester-type Prodrugs].ReviewYakugaku zasshi : Journal of the Pharmaceutical Society of Japan · 2020Ohura KDOI: 10.1248/yakushi.19-00225
- Emerging trends in stereoselective glycosyl ester synthesis.ReviewAdvances in carbohydrate chemistry and biochemistry · 2025Maheshwari M, Hussain NDOI: 10.1016/bs.accb.2025.09.001
- Palladium-Catalyzed Tandem Ester Dance/Decarbonylative Coupling Reactions.Organic letters · 2022Kubo M, Inayama N, Ota E et al.DOI: 10.1021/acs.orglett.2c01432
- Steryl Ester Formation and Accumulation in Steroid-Degrading Bacteria.Applied and environmental microbiology · 2020Holert J, Brown K, Hashimi A et al.DOI: 10.1128/AEM.02353-19
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Article · Français
En chimie, la fonction ester désigne un groupement caractéristique formé d'un atome lié simultanément à un atome d'oxygène par une double liaison et à un groupement alkoxy. Lorsque l'atome lié est un atome de carbone, on parle d'ester carboxylique, dont la forme générale est R-COO-R'. Cependant, ce peut être aussi un atome de soufre (par exemple dans les esters sulfuriques, sulféniques, etc.), d'azote (esters nitriques, etc.), de phosphore (esters phosphoriques, phosphoniques, phosphéniques, etc.), etc. En fait, tout oxoacide organique, inorganique ou minéral a la capacité de former des esters. Les esters carboxyliques sont des dérivés des acides carboxyliques, ils résultent très généralement de l'action d'un alcool sur ces acides avec élimination d'eau. Les fonctions esters se retrouvent dans de nombreuses molécules biologiques, notamment les triglycérides. Les esters carboxyliques ont souvent une odeur agréable et sont souvent à l'origine de l'arôme naturel des fruits. Ils sont aussi beaucoup utilisés pour les arômes synthétiques et dans la parfumerie.
Abstract from DBpedia / Wikipedia · CC BY-SA
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