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...e in [[organic synthesis]]. A useful application is in the preparation of aryl iodides from [[arenediazonium salts]].<ref>L. G. Wade, ''Organic Chemistry'

...ocation. Acetic acid is the solvent of choice when [[redox|reducing]] an [[aryl]] [[Nitro compound|nitro]]-group to [[aniline]] using [[palladium-on-carbon

...high temperatures. They contain the subunit [[arene|aryl]]-SO₂-aryl, the defining feature of which is the [[sulfone]] group. Polysulfones were

...rene Trimer May Increase Thyroid Hormone Levels via Down-Regulation of the Aryl Hydrocarbon Receptor (AhR) Target Gene UDP-Glucuronosyltransferase|journal=

...rings, a total of 5 rings, and 4 ether linkages. Meta substitution of the aryl rings in these materials is most common and often desired. Longer chain an

...s for ''meta''- , and '''''p''-''' stands for ''para''- . All three are [[aryl]] [[amine]]s whose [[chemical structure]]s are similar to [[aniline]] excep ...o those of [[aniline]] and toluidines have properties in common with other aryl (often incorrectly referred to as aromatic) amines. Due to the amino group

...| pmc = 1575965}}</ref> Most bio-active derivatives bear a substituent ([[aryl]] or [[alkyl]] group) on the carbon between the nitrogen centers. Some gene

...nds have the formulae R_3-xAsCl_x (where R = alkyl and aryl, and x = 0,1,2). Cacodylic acid which is of historic and practical interes

...to prepare Ni[S₂C₂Ar₂]₂ (Ar = aryl).

...diketimine]]s wherein the O atoms in acetylacetone are replaced by NR (R = aryl, alkyl).

...C-PO(OH)₂ or C-PO(OR)₂ groups (where R=[[alkyl]], [[aryl]]). [[Bisphosphonates]] were first synthesized in 1897 by Von Baeyer and Ho

In the tetra[[aryl]]borates, the [[electron density|negative charge]] is symmetrically distrib

...on examples include derivatives of the above inorganic ligands (R = alkyl, aryl):

...mine" is spelled this way due to historical reasons; in contrast, alkyl or aryl bearing ligands are spelled with a single "m".

...absorbance characteristics of the different [[chromophore|chromophoric]] 2-aryl substituents, affects the decarboxylation mechanism. While [[ibuprofen]] is

...version of the same reaction<ref>''Palladium-Catalyzed Ring Enlargement of Aryl-Substituted Methylenecyclopropanes to Cyclobutenes'' Min Shi, Le-Ping Liu,

...formylation of activated [[aromatic rings]] such as [[phenols]], producing aryl [[aldehyde]]s in a reaction known as the [[Reimer-Tiemann reaction]]. Alter