Efficient and economic halogenation of aryl amines via arenediazonium tosylate salts; Tetrahedron Letters; Vol. 66, iss. 37

Détails bibliographiques
Parent link:Tetrahedron Letters: Scientific Journal
Vol. 66, iss. 37.— 2010.— [P. 7418–7422]
Autres auteurs: Young Min Lee, Mi Eun Moon, Filimonov V. D. Viktor Dmitrievich, Ki-Whan Chi
Résumé:Title screen
Arenediazonium tosylate salts have been successfully employed as a new and efficient reagent in halogenation reactions. A novel and economic protocol has been developed for the bromination and chlorination of various anilines using arenediazonium tosylate salts. A wide variety of reaction conditions were studied in acetonitrile at either room temperature or 60 °C in the presence or absence of catalyst with good to excellent yields. A surprising result showed the formation of acetanilides as a major product of aniline and methyl-substituted aniline halogenations in high yields
Режим доступа: по договору с организацией-держателем ресурса
Langue:anglais
Publié: 2010
Sujets:
Accès en ligne:http://www.sciencedirect.com/science/article/pii/S0040402010010446
Format: Électronique Chapitre de livre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=636585

MARC

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300 |a Title screen 
320 |a [Referenses: p.7422 (29 tit.)] 
330 |a Arenediazonium tosylate salts have been successfully employed as a new and efficient reagent in halogenation reactions. A novel and economic protocol has been developed for the bromination and chlorination of various anilines using arenediazonium tosylate salts. A wide variety of reaction conditions were studied in acetonitrile at either room temperature or 60 °C in the presence or absence of catalyst with good to excellent yields. A surprising result showed the formation of acetanilides as a major product of aniline and methyl-substituted aniline halogenations in high yields 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
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