Microwave-Assisted Solvent-Free Arylation of Amino acids with Halogenobenzenes
dc.date.accessioned | 2019-02-08T08:51:44Z | |
dc.date.available | 2019-02-08T08:51:44Z | |
dc.date.issued | 2018 | |
dc.description.abstract | The 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.uri | https://ir.unilag.edu.ng/handle/123456789/3655 | |
dc.language.iso | en | en_US |
dc.subject | Research Subject Categories::NATURAL SCIENCES | en_US |
dc.title | Microwave-Assisted Solvent-Free Arylation of Amino acids with Halogenobenzenes | en_US |
dc.type | Article | en_US |