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Synthesis of N-Aryl Phenylglycine Ο-Alkyl Esters and Its Substitution of Ester Moiety  

박명숙 (덕성여자대학교 약학대학)
박해선 (덕성여자대학교 약학대학)
Publication Information
YAKHAK HOEJI / v.47, no.5, 2003 , pp. 276-282 More about this Journal
Abstract
For the development of new synthetic method for unnatural amino acid esters, N-aryl phenylglycine Ο-alkyl esters 4a∼i were synthesized through esterification, bromination, C-N bond formation from commercially available phenylacetic acids. An efficient and practical reaction condition for esters 2a∼c was that the starting materials 1a∼c were refluxed in absolute methanol for 3 hours with catalytic concentrated hydrosulfuric acid. In addition, bromines 3a∼c were formated for 3h in dichloromethane at rt with N-bromosuccinimide. Bromines 3a∼c were also converted to 4a∼i through substitution of arylamines during refluxing for 24 hours in ethanol with triethylamine. Interestingly, ethyl esters 5a∼c were formed via transesterification reaction when the p-sulfamylanilino group was used as a nucleophile in ethanol solvent.
Keywords
N-aryl phenylglycine Ο-alkyl esters; substitution of ester moiety; unnatural amino acids;
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Times Cited By KSCI : 1  (Citation Analysis)
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