Microwave-Assisted Solvent-Free Arylation of Amino acids with Halogenobenzenes

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dc.contributor.authorSowole, M.A.
dc.contributor.authorAdebisi, A.B.
dc.contributor.authorOlasupo, I.A.
dc.contributor.authorIzunobi, J.U.
dc.contributor.authorFamiloni, O.B.
dc.date.accessioned2019-08-23T14:53:08Z
dc.date.available2019-08-23T14:53:08Z
dc.date.issued2018-06-21
dc.description.abstractThe solventless microwave-assisted arylation and heteroarylation of different aliphatic and cyclic amino acids 2a–e were carried out on activated, substituted o-nitrohalogenobenzenes 1a–h and 2-chloro-3-nitropyridine 1i, in the presence of potassium carbonate and potassium fluoride for 0.5 h at 70 W, to give substituted N-(o-nitrophenyl)amino-2-carboxylic acid 3–16 and N-(m-nitropyridyl)amino-2-carboxylic acid 17–18 adducts in yields ranging from 5–98% .en_US
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/4646
dc.language.isoenen_US
dc.publisherChemical Society of Nigeriaen_US
dc.subjectamino acids, arylation, halogenobenzenes, microwave synthesisen_US
dc.titleMicrowave-Assisted Solvent-Free Arylation of Amino acids with Halogenobenzenesen_US
dc.typeArticleen_US
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