One-Pot Synthesis of Chloropyridines from Aminopyridines via Diazotization; Key Engineering Materials; Vol. 712 : Advanced Materials for Technical and Medical Purpose (AMTMP 2016)

التفاصيل البيبلوغرافية
Parent link:Key Engineering Materials: Scientific Journal
Vol. 712 : Advanced Materials for Technical and Medical Purpose (AMTMP 2016).— 2016.— [P. 273-276]
المؤلف الرئيسي: Lesina Yu. A. Yuliya Aleksandrovna
مؤلف مشترك: Национальный исследовательский Томский политехнический университет (ТПУ) Институт физики высоких технологий (ИФВТ) Кафедра биотехнологии и органической химии (БИОХ)
مؤلفون آخرون: Beysembay P. Perizat, Kassanova A. Assiya
الملخص: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
اللغة:الإنجليزية
منشور في: 2016
سلاسل:Materials and Technologies for Biomedical Application and Environmental Engineering
الموضوعات:
الوصول للمادة أونلاين:http://dx.doi.org/10.4028/www.scientific.net/KEM.712.273
التنسيق: الكتروني فصل الكتاب
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=651342
الوصف
الملخص: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