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

dc.date.accessioned2019-02-08T08:51:44Z
dc.date.available2019-02-08T08:51:44Z
dc.date.issued2018
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/123456789/3655
dc.language.isoenen_US
dc.subjectResearch Subject Categories::NATURAL SCIENCESen_US
dc.titleMicrowave-Assisted Solvent-Free Arylation of Amino acids with Halogenobenzenesen_US
dc.typeArticleen_US
Files
Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
JCSN 2018 38 345-352.pdf
Size:
617.69 KB
Format:
Adobe Portable Document Format
Description:
License bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: