A Novel and Simple Synthesis of Ethers of Hydroxypyridines with Hexafluoropropan-2-ol via Diazotization of Aminopyridines and Aminoquinolines Under Acid-Free Conditions

Bibliographic Details
Parent link:	Chemistry of Heterocyclic Compounds Vol. 58, iss. 12.— 2022.— [P. 721-726]
Corporate Author:	Национальный исследовательский Томский политехнический университет Инженерная школа новых производственных технологий Научно-образовательный центр Н. М. Кижнера
Other Authors:	Filimonov V. D. Viktor Dmitrievich, Sanzhiev A. N. Aldar Nikolaevich, Gulyaev R. O. Roman Olegovich, Krasnokutskaya E. A . Elena Aleksandrovna, Bondarev A. A. Aleksandr Aleksandrovich
Summary:	Title screen Herein, we report the first example of diazotization of aminopyridines and aminoquinolines with t-BuONO in hexafluoropropan-2-ol in the absence of acids or other initiators. For aminopyridines, this reaction is the first general route toward 2-, 3-, and 4-[(1,1,1,3,3,3-hexafluoropropan-2-yl)oxy]pyridines. Режим доступа: по договору с организацией-держателем ресурса
Published:	2022
Subjects:	электронный ресурс труды учёных ТПУ aminopyridines aminoquinolines anilines ethers 1,1,1,3,3,3-hexafluoropropan-2-ol diazotization
Online Access:	https://doi.org/10.1007/s10593-023-03148-4
Format:	Electronic Book Chapter
KOHA link:	https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=669321

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