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...ast2=Henkes|first3=Roland|last3=Rossbacher|first4=Hartmut|last4=Höke|title=Amines, Aliphatic|year=2005|doi=10.1002/14356007.a02_001}}</ref> ...ination of alpha-halo carboxylic acids that do permit synthesis of primary amines with ammonia.<ref>[[Organic Syntheses]], Coll. Vol. 1, p.48 (1941); Vol. 4, ...

...compounds]].<ref name=Ullmann>{{Ullmann|doi=10.1002/14356007.a02_001|title=Amines, Aliphatic|year=2000|last1= Eller|first1=Karsten|last2=Henkes|first2=Erhard *Cyanoethylation of amines.<ref>{{cite journal |doi=10.15227/orgsyn.036.0006|title=N-2-Cyanoethylanili ...

...eactions in which [[ammonia]] is a reactant|chemical reactions involving [[amines]]|aminolysis}} ...monolysis reactions can be conducted with [[organic compound]]s to produce amines (molecules containing a [[nitrogen]] atom with a [[lone pair]], :N),<ref>{{ ...

...ies of two primary-amine oxidases from the yeast Candida boidinii grown on amines as sole nitrogen source | journal = The Biochemical Journal | volume = 199 Like [[monoamine oxidase]] (MAO), SSAO can deaminate short-chain primary amines, but is insensitive to MAO inhibitors. [[Semicarbazide]] inhibits the enzym ...

...te journal | vauthors = Eady RR, Large PJ | title = Microbial oxidation of amines. Spectral and kinetic properties of the primary amine dehydrogenase of Pseu ...

...e (Escherichia coli) | date = 1971 | title = Metabolism of Amino Acids and Amines Part B | series = Methods Enzymol. | volume = 17B | pages = 134&ndash;139 ...

*[[Hydroamination]] - addition of [[amines]] to alkenes ...

...al=[[J. Am. Chem. Soc.]]|title=Derivatives of the methylchlorosilanes. IV. Amines|volume=68|issue=2|pages=241–244|date= 1946|doi=10.1021/ja01206a028}}</ref> ...oc.]]|title=Preparation of tris(trimethylsilyl)- and tris(trimethylstannyl)amines|volume=86|issue=2|pages=305|date= 1964|doi=10.1021/ja01056a057}}</ref> ...

...somewhat with the particular amine being used. For one of the more common amines, monoethanolamine (MEA) denoted as '''''RNH₂''''', the chemistry ...

...t1=A|title=Controlled reduction of nitroalkanes to alkyl hydroxylamines or amines by samarium diiodide|journal=Tetrahedron Letters|volume=32|pages=1699–1702| ...are reduced by samarium(II) iodide to the corresponding hydroxylamines or amines. Nitro compounds may be selectively reduced to either product, depending on ...

...d very well, but the creation of fulminating gold and other precious metal amines limits its widespread use.<ref>{{cite journal|last1=Macaskie|first1=L.E.|la ...

...leophile|nucleophilic]] terminal amine groups of primary [[Amine|aliphatic amines]] such as [[Ornithine|L-ornithine]].<ref name="Franceschini_2012" /> The en ...

...arbonyl groups. [[Carboxylic acid]] derivatives, acetals, [[thioacetal]]s, amines, alcohols, and isolated double bonds are all inert to Al/Hg. Selective desu ...rtiary [[nitrile]]s (primary and secondary nitriles give the corresponding amines in addition to decyanated products),<ref>{{cite journal|last1=Arapakos|firs ...

...ond forming reactions—visible light mediated oxidative phosphonylations of amines|journal=Chemical Communications|year=2011|volume=47|issue=30|pages=8679–81| ...raphene oxide and Rose Bengal: oxidative C–H functionalisation of tertiary amines using visible light|journal=Green Chemistry|year=2011|volume=13|issue=12|pa ...

[[Category:Amines]] ...

...</ref><ref>{{cite journal | title = First asymmetric oxidation of tertiary amines by cyclohexanone monooxygenase | vauthors = Ottolina G, Bianchi S, Belloni ...

...sidewalls (e.g. with diazonium, simple alkyls, hydrogen, ozone/oxygen, and amines). Multiwall nanotubes are typically used for their rigidity. Because of the ...

...household cleaners. Some common cationic surfactants head groups include [[amines]] and quaternary [[ammonium]] ions. ...