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- {{Short description|Chemical compounds with at least one palladium atom}} ...>2+</sup>. [[Palladium(III) compounds]] have also been reported. Palladium compounds are frequently used as catalysts in [[cross-coupling reaction]]s such as th ...6 KB (788 words) - 12:03, 7 February 2025
- ...ide]] in ethanol can react with tetraphenyllead and substitute some of the phenyl groups to chlorine atoms:<ref name="Bähr" /> ....<ref name="Richard W. Weiss">{{cite book| author=Richard W. Weiss | title=Compounds of Germanium, Tin, and Lead, including Biological Activity and Commercial A ...5 KB (605 words) - 15:21, 24 January 2024
- ...strate. The method is used in the [[organic synthesis|synthesis of organic compounds]].<ref name=Ullmann>{{Ullmann|doi=10.1002/14356007.a02_001|title=Amines, Al ...ussRev>{{cite journal|title=Phosphine in the synthesis of organophosphorus compounds|first1=Boris A. |last1=Trofimov|first2=Svetlana N. |last2=Arbuzova|first3=N ...4 KB (526 words) - 11:31, 4 January 2024
- | PIN = Dimethyl(phenyl)phosphane .../sub>)(CH<sub>3</sub>)<sub>2</sub>. The [[phosphorus]] is connected to a [[phenyl]] group and two [[methyl]] groups, making it the simplest aromatic alkylpho ...7 KB (931 words) - 10:10, 2 September 2024
- {{correct title|reason=bracket|Tetrakis[3,5-bis(trifluoromethyl)phenyl]borate}} ...Safe Preparation and Purification of Sodium Tetrakis[(3,5-trifluoromethyl)phenyl]borate (NaBArF<sub>24</sub>): Reliable and Sensitive Analysis of Water in S ...11 KB (1,478 words) - 06:49, 25 June 2024
- ...[[catalyst]]s in [[organic reaction]]s.<ref>''Synthesis of Organometallic Compounds: A Practical Guide'' Sanshiro Komiya Ed. S. Komiya, M. Hurano 1997</ref> Stable organorhodium compounds and transient organorhodium intermediates are used as catalyst such as in o ...10 KB (1,353 words) - 12:18, 20 February 2025
- '''Organoantimony chemistry''' is the [[chemistry]] of [[chemical compound|compounds]] containing a [[carbon]] to [[antimony]] (Sb) [[chemical bond]]. Relevant ...ompound|organolithium]] or [[Grignard reaction|Grignard]] reagents to give compounds of the form R<sub>3</sub>Sb: ...8 KB (1,163 words) - 22:25, 7 February 2025
- ...nd thus can be used for alpha-[[hydroxylation]] of [[carbonyl]]-containing compounds.<ref>{{Cite journal | doi = 10.15227/orgsyn.064.0127| title = HYDROXYLATION ...=Transition-metal peroxide reactions. Synthesis of α-hydroxycarbonyl compounds from enolates|journal=The Journal of Organic Chemistry|volume=43|issue=2|pa ...7 KB (958 words) - 15:31, 8 February 2025
- {{Short description|Methods of hydrogenation and hydrogenolysis of organic compounds}} ...st2=Henry S. |title=Carbonium ion-silane hydride transfer reactions. II. 2-Phenyl-2-norbornyl cation |journal=The Journal of Organic Chemistry |date=January ...13 KB (1,710 words) - 17:57, 15 August 2024
- ...amarium(II) iodide''' involve the conversion of various classes of organic compounds into reduced products through the action of [[samarium(II) iodide]], a mild *α-Functionalized carbonyl compounds ...17 KB (2,375 words) - 21:27, 29 August 2024
- ...ies showed that sonocatalysis could increase [[pyrazole]] synthesis yield, compounds that has [[antimicrobial]], [[Antihypertensive drug|antihypertensive]], [[a ...e-1-carbothioamide_sous_sonocatalyse.png|center|thumb|700x700px|3-methyl-5-phenyl-4,5-dihydro-1H-pyrazole-1-carbothioamide synthesis under sonocatalysis]] ...16 KB (2,109 words) - 17:19, 10 December 2024
- ...is an analytical technique used to detect and identify fluorine-containing compounds. <sup>19</sup>F is an important nucleus for [[NMR spectroscopy]] because o ...hemical shifts span a range of about 800 ppm. For ''organo''fluorine compounds the range is narrower, being about −50 to −70 ppm (for CF<sub>3</sub> ...15 KB (2,084 words) - 02:36, 5 October 2024
- ...urnal |last=Schoenleber |first=Andreas |date=2011 |title=Organic molecular compounds with modulated crystal structures |journal=Zeitschrift für Kristallographie ...phenyl]] molecule is a simple organic molecular compound consisting of two phenyl rings bonded by a central C-C single bond, which exhibits a modulated molec ...7 KB (966 words) - 21:44, 30 September 2024
- ...eaction]] using [[methylenetriphenylphosphorane]] with an aldehyde (Ph = [[phenyl]], {{chem2|C6H5}}):<ref>{{cite journal |author=Eric J. Leopold|doi=10.15227 ...=81|year=1987|doi=10.15227/orgsyn.065.0081|title=Methylenation of Carbonyl Compounds: (+)-3-Methylene-''cis-p''-menthane}}</ref><ref>{{cite journal | last1 = Ma ...8 KB (1,071 words) - 08:05, 13 April 2024
- ...,13,15-octa-phenyl-penta-cyclo-[9.5.1.13,9.15,15.17,13]octa-siloxane (octa-phenyl-POSS)|journal=Acta Crystallogr C|volume=70|issue=10|pages=971–974|doi=10.11 ...e been reported, first by Brown. High molecular weight tractable polymeric phenyl silsesquioxane featured a ladder-type structure.<ref name=Brown1960>{{cite ...34 KB (4,467 words) - 01:43, 9 November 2024
- ...les: [[aldehyde]]s and [[ketone]]s, [[Carboxylic Acid Derivatives#Carbonyl compounds|carboxylic acid-derivatives]], and the carbon-carbon double bonds of [[alke ...lision) of a [[nucleophile]] on a [[trigonal]] [[Saturated and unsaturated compounds|unsaturated]] center of an [[electrophile|electrophilic]] [[molecule]] (the ...36 KB (5,159 words) - 09:29, 26 February 2025
- ...common RAFT-processes are carried out in the presence of thiocarbonylthio compounds that act as radical buffers. ...nvention of high-speed living radical polymerization using organotellurium compounds and azo-initiators |journal=J. Am. Chem. Soc. |volume=125 |issue=29 |pages= ...26 KB (3,465 words) - 09:48, 30 December 2023
- ...bstrate lowering the amount of the monophenols that bind. These inhibitory compounds added to the produce keep it fresh for longer periods of time by decreasing ...dopamine transporter protects against the oxidation of MPTP to MPP+. A few compounds have been tested for their ability to inhibit oxidation of MPTP to MPP+ inc ...22 KB (3,354 words) - 07:23, 6 August 2024
- |title=Pentakis(trifluoromethyl)phenyl, a Sterically Crowded and Electron-withdrawing Group: Synthesis and Acidity ...tautomerism]]. This effect is especially pronounced in [[1,3-dicarbonyl]] compounds that can form [[hydrogen-bonding|hydrogen-bonded]] enols. The [[equilibrium ...17 KB (2,405 words) - 20:14, 18 October 2024
- {{Short description|Chemical compounds with the same molecular formula but different atomic arrangements}} For example, there are three distinct compounds with the molecular formula <chem>C3H8O</chem>: ...34 KB (4,977 words) - 11:52, 26 February 2025