One-Pot Synthesis of Chloropyridines from Aminopyridines via Diazotization

One-Pot Synthesis of Chloropyridines from Aminopyridines via Diazotization

Dades bibliogràfiques
Parent link:Key Engineering Materials: Scientific Journal
Vol. 712 : Advanced Materials for Technical and Medical Purpose (AMTMP 2016).— 2016.— [P. 273-276]
Autor principal: Lesina Yu. A. Yuliya Aleksandrovna
Autor corporatiu: Национальный исследовательский Томский политехнический университет (ТПУ) Институт физики высоких технологий (ИФВТ) Кафедра биотехнологии и органической химии (БИОХ)
Altres autors: Beysembay P. Perizat, Kassanova A. Assiya
Sumari:Title screen
A method for synthesis of chloropyridines from pyridinyl trifluoromethanesulfonates in acetonitrile in the presence of hydrochloric acid was developed. One-pot synthesis of chloropyridines from aminopyridines via diazotization was presented. Pyridyl triflates were obtained in this reaction in situ. This method provides good yields of the target products.
Режим доступа: по договору с организацией-держателем ресурса
Publicat: 2016
Col·lecció:Materials and Technologies for Biomedical Application and Environmental Engineering
Matèries:
электронный ресурс
труды учёных ТПУ
аминопиридины
хлорпиридины
диазотирование
синтез
соляная кислота
Accés en línia:http://dx.doi.org/10.4028/www.scientific.net/KEM.712.273
Format: Electrònic Capítol de llibre
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=651342
Descripció
Sumari:Title screen
A method for synthesis of chloropyridines from pyridinyl trifluoromethanesulfonates in acetonitrile in the presence of hydrochloric acid was developed. One-pot synthesis of chloropyridines from aminopyridines via diazotization was presented. Pyridyl triflates were obtained in this reaction in situ. This method provides good yields of the target products.
Режим доступа: по договору с организацией-держателем ресурса
DOI:10.4028/www.scientific.net/KEM.712.273

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