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- In [[organic chemistry]], '''borate esters''' are [[organoboron compound]]s which are conveniently prepared by the sto ...|volume=78|issue=15|pages=3613–3614|doi=10.1021/ja01596a015}}</ref> Borate esters are volatile and can be purified by distillation. This procedure is used fo ...3 KB (469 words) - 04:50, 8 February 2023
- ...food preservatives, food additives, and other products. A class of sucrose esters with highly substituted hydroxyl groups, [[olestra]], is also used as a fat ...ucrose octapalmitate and sucrose octastearate. Both are sucrose fatty acid esters. ...26 KB (3,905 words) - 07:56, 22 January 2025
- '''Fatty acyl-CoA esters''' are fatty acid derivatives formed of one [[fatty acid]], a 3'-phospho-[[ Long-chain acyl-CoA esters are substrates for a number of important enzymatic reactions and play a cen ...3 KB (428 words) - 12:54, 10 October 2024
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- In [[organic chemistry]], '''borate esters''' are [[organoboron compound]]s which are conveniently prepared by the sto ...|volume=78|issue=15|pages=3613–3614|doi=10.1021/ja01596a015}}</ref> Borate esters are volatile and can be purified by distillation. This procedure is used fo ...3 KB (469 words) - 04:50, 8 February 2023
- '''Fatty acyl-CoA esters''' are fatty acid derivatives formed of one [[fatty acid]], a 3'-phospho-[[ Long-chain acyl-CoA esters are substrates for a number of important enzymatic reactions and play a cen ...3 KB (428 words) - 12:54, 10 October 2024
- ...chem2|R\sONO2}}, where R stands for any [[organyl]] group. They are the [[esters]] of [[nitric acid]] and [[alcohols]]. A well-known example is [[nitroglyce ...n Dolah |first3=Robert W. |date=1955-06-01 |title=The Chemistry of Nitrate Esters |url=https://pubs.acs.org/doi/abs/10.1021/cr50003a001 |journal=Chemical Rev ...5 KB (722 words) - 22:29, 11 November 2024
- ...acyltransferase capable of synthesizing benzylbenzoate and other volatile esters in flowers and damaged leaves of Clarkia breweri | journal = Plant Physiolo ...2 KB (191 words) - 12:49, 9 February 2025
- ...acyltransferase capable of synthesizing benzylbenzoate and other volatile esters in flowers and damaged leaves of Clarkia breweri | journal = Plant Physiolo ...2 KB (212 words) - 13:22, 26 August 2023
- ...droxyls (hydroxyl nitriles and carbohydrates), carbonyl (aldehydes/ketones/esters/alcohols), and sulfur (sulfonyl derivatives) can all undergo ammonolysis in === Mechanism: Ammonolysis of Esters === ...10 KB (1,351 words) - 16:24, 19 January 2025
- ...food preservatives, food additives, and other products. A class of sucrose esters with highly substituted hydroxyl groups, [[olestra]], is also used as a fat ...ucrose octapalmitate and sucrose octastearate. Both are sucrose fatty acid esters. ...26 KB (3,905 words) - 07:56, 22 January 2025
- ...ented in 1990 by [[Tohru Fukuyama]].<ref>''Facile reduction of ethyl thiol esters to aldehydes: application to a total synthesis of (+)-neothramycin A methyl ...2 KB (329 words) - 22:21, 26 August 2023
- ...s and [[ketone]]s, or more rarely, [[Enol ether|enol ethers]] from [[Ester|esters]] or [[Enamine|enamines]] from [[Amide|amides]]. Ketones and esters can be methylenated at the α position to give α,β-unsaturated carbonyl prod ...8 KB (1,071 words) - 08:05, 13 April 2024
- 5 KB (725 words) - 02:32, 2 December 2024
- ...atalyzes the efficient in vitro conversion of p-coumaryl/coniferyl alcohol esters into the allylphenols chavicol/eugenol, but not the propenylphenols p-anol/ ...4 KB (445 words) - 15:00, 26 August 2023
- ...nerically as [[octanol]]s. 1-Octanol is manufactured for the synthesis of esters for use in [[perfume]]s and [[flavoring]]s. It has a pungent odor. [[Ester ...8 KB (1,003 words) - 11:46, 11 January 2024
- ...on of Hydroxide Ion with Other Nucleophilic Reagents toward Alkyl Halides, Esters, Epoxides and Acyl Halides|journal=Journal of the American Chemical Society ...st2=Carriuolo|first2=Joan|title=Reactivity of Nucleophilic Reagents toward Esters|journal=Journal of the American Chemical Society|date=April 1960|volume=82| ...10 KB (1,432 words) - 14:19, 31 May 2023
- ;Esters Esters may be reduced to alcohols under conditions of nucleophilic activation with ...13 KB (1,710 words) - 17:57, 15 August 2024
- |Fatty acyl-CoA esters<ref name=":11" /> |Fatty acyl-CoA esters<ref name=":15" /> ...18 KB (2,364 words) - 21:58, 21 February 2025
- 4 KB (565 words) - 13:03, 7 January 2022
- *Tin oxalate is used as a catalyst in the production of organic esters and plasticizers.<ref name="AA">{{cite web |title=814-94-8 - Tin(II) oxalat ...4 KB (551 words) - 02:58, 1 December 2023
- ...oric acid') of the formula H<sub>4</sub>B<sub>2</sub>O<sub>4</sub> and its esters}}</ref> The [[methanol]] used in this process can be recycled: ...5 KB (623 words) - 22:16, 18 September 2024
- ...C.A., 93, 239789w (1980)].</ref> Electron-rich carbonyl compounds, such as esters and amides, do not react with DAST or other aminosulfuranes. Alkali and tetraalkylammonium fluorides can be used to displace sulfonate esters; however, these reactions require higher temperatures than aminosulfurane f ...11 KB (1,487 words) - 22:33, 21 December 2023
- ...irst2=Michael|last3=Subramanian|first3=L. R.|title=Perfluoroalkanesulfonic Esters: Methods of Preparation and Applications in Organic Chemistry|journal=Synth ...5 KB (591 words) - 17:17, 29 September 2023