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Amine activation

Tijdschriftbijdrage - Tijdschriftartikel

Ondertitel:N-arylamino acid amide synthesis from isothioureas and amino acids
N-arylamino acid amides have been synthesized via a novel method based on N-arylamine activation into isothioureas followed by reaction with amino acids under iron catalysis. The activated N-arylamines are easily prepared using a three-component reaction with commercial reagents, tert-butylisocyanide and S-phenyl benzenethiosulfonate. The protocol shows a broad functional group compatibility, with respect to side chain functionality of the amino acid (e. g. aliphatic and aromatic OH, (hetero)aromatic NH, amide NH, thioether), and the chiral amino acids do not undergo epimerization. The mechanism of the new amide synthesis has been studied.
Tijdschrift: Advanced synthesis and catalysis
ISSN: 1615-4150
Volume: 359
Pagina's: 2481 - 2498
Jaar van publicatie:2017
Trefwoorden:A1 Journal article
BOF-keylabel:ja
BOF-publication weight:10
CSS-citation score:1
Authors from:Higher Education
Toegankelijkheid:Open