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- |Type = Organic redox reaction The '''Fukuyama reduction''' is an [[organic reaction]] and an [[organic reduction]] in which a [[thioester]] is reduced to an [[aldehyde]] by a [[s ...2 KB (329 words) - 22:21, 26 August 2023
- ...resonance effects in electrophilic reactions of para- and meta-substituted organic compounds. This equation does so by introducing a new term to the original ...sigma;<sup>−</sup>}} represent the Hammett substituent constants for reactions in which positive or negative charges are built up at the reactive center, ...6 KB (928 words) - 04:05, 16 June 2023
- ...9.conrr179 |chapter=Darzens Halogenation |title=Comprehensive Organic Name Reactions and Reagents |date=2010 |pages=846–847 |isbn=9780471704508 }}</ref> {{Organic reactions}} ...3 KB (382 words) - 06:58, 23 April 2024
- ...047084289X.ra026|chapter=Acetyl Cyanide|title=Encyclopedia of Reagents for Organic Synthesis|year=2001|last1=Morris|first1=Joel|isbn=0471936235}}</ref> ==Reactions== ...3 KB (434 words) - 09:42, 9 October 2022
- {{short description|Organic reaction between amine and alkyl halide}} '''Amine alkylation''' ('''amino-dehalogenation''') is a type of [[organic reaction]] between an [[alkyl halide]] and [[ammonia]] or an [[amine]].<ref ...6 KB (841 words) - 01:53, 9 July 2022
- ...position of the respective phases (i.e. without noticeable electrochemical reactions taking place at the interface). An ITIES system is polarised if the distrib ...alt such as [[tetrabutylammonium]] [[tetraphenylborate]] dissolved in an [[organic solvent]] [[immiscible]] with water such as [[nitrobenzene]], or [[1,2-dich ...5 KB (819 words) - 14:39, 6 October 2022
- ...iple''') observes that the difference in [[activation energy]] between two reactions of the same family is proportional to the difference of their [[enthalpy of ...that serves as an efficient way to calculate [[activation energy]] of many reactions within a distinct family. The [[activation energy]] may be used to characte ...3 KB (340 words) - 14:24, 31 July 2024
- ...st number of atoms.<ref>{{cite book |title= The Vocabulary And Concepts Of Organic Chemistry|last= Orchin|first=Milton |year= 2005|publisher= John Wiley & Son ...ng properties:<ref name=Jones>{{cite book |title= Physical and Mechanistic Organic Chemistry|last= Yardley Jones|first=Richard Arnold |year= 1979|publisher= C ...3 KB (387 words) - 12:23, 17 July 2023
- ...anic substrate. The method is used in the [[organic synthesis|synthesis of organic compounds]].<ref name=Ullmann>{{Ullmann|doi=10.1002/14356007.a02_001|title= ...oi=10.15227/orgsyn.038.0014|title=3-(o-Chloroanilino)propionitrile|journal=Organic Syntheses|year=1958|volume=38|page=14|author=S. A. Heininger}}</ref> ...4 KB (526 words) - 11:31, 4 January 2024
- ...Akira |author2-link=Akira Suzuki |title=Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds. |journal=[[Chemical Reviews]] |year=1995 |volume= ...ion]]). After [[transmetalation]] with an [[organometallic compound]], two organic ligands to Pd<sup>2+</sup> may exit the palladium complex and combine, form ...6 KB (788 words) - 12:03, 7 February 2025
- {{Short description|Organic reaction which inserts an alkene into a C-H bond of ethylene}} In [[organic chemistry]], '''hydrovinylation''' is the formal [[Insertion reaction|inser ...7 KB (895 words) - 18:36, 18 November 2024
- ...na | last3 = García-Blanco | first3 = Francisco | journal = The Journal of Organic Chemistry | volume = 64 | issue = 17 | pages = 6512–6514}}</ref> ...= The Correlation of Solvolysis Rates and the Classification of Solvolysis Reactions into Mechanistic Categories | journal= [[J. Am. Chem. Soc.]]|year = 1951 | ...7 KB (963 words) - 20:01, 2 April 2023
- ...nic molecules that can exhibit more complex, multi-step disproportionation reactions. ...9. {{doi|10.1021/j100266a042}}</ref> In the most common disproportionation reactions, a hydrogen atom is taken, or abstracted by the acceptor as the donor molec ...9 KB (1,233 words) - 22:56, 8 February 2024
- {{Short description|Israeli organic chemist (1930–2024)}} | field = [[Chemical synthesis|Synthetic organic chemistry]], [[Heterocyclic compound|Heterocycles]] ...8 KB (1,048 words) - 06:34, 1 February 2025
- ...MPA(MoOPH): 3-HYDROXY-1,7,7-TRIMETHYLBICYCLO[2.2.1]HEPTAN-2-ONE| journal = Organic Syntheses| volume = 64| pages = 127| year = 1986}}</ref> Other reagents use ...of α-hydroxycarbonyl compounds from enolates|journal=The Journal of Organic Chemistry|volume=43|issue=2|pages=188–196|doi=10.1021/jo00396a002|issn=0022 ...7 KB (958 words) - 15:31, 8 February 2025
- ...ents including, [[benzene]]. It is a [[reagent]] used in the synthesis of organic and inorganic triflates. ==Reactions== ...5 KB (591 words) - 17:17, 29 September 2023
- In [[organic chemistry]], a '''nitrate ester''' is an organic [[functional group]] with the formula {{chem2|R\sONO2}}, where R stands for ==Synthesis and reactions== ...5 KB (722 words) - 22:29, 11 November 2024
- ...vatization]] to improve the quantitative measurement of [[Organic compound|organic]] [[Analyte|analytes]]. It is used in [[gas chromatography]] (GC), after th The reactor contains [[catalyst]]s that converts all of the carbon atoms of organic molecules in GC column effluents into [[methane]] before reaching the FID. ...9 KB (1,358 words) - 21:15, 10 January 2025
- In [[organic chemistry]], '''methylenation''' is a [[chemical reaction]] that inserts a ...l=https://pubs.acs.org/doi/abs/10.1021/jo01084a635 |journal=The Journal of Organic Chemistry |language=en |volume=24 |issue=2 |pages=264–265 |doi=10.1021/jo01 ...8 KB (1,071 words) - 08:05, 13 April 2024
- {{short description|Organic compounds of the form B(OR)₃ or B₃O₃(OR)₃}} In [[organic chemistry]], '''borate esters''' are [[organoboron compound]]s which are co ...3 KB (469 words) - 04:50, 8 February 2023