A new transformation of aminopyridines upon diazotization in acetonitrile with the formation of N-pyridinylacetamides / A. A. Chudinov [et al.]
Уровень набора: Russian Chemical Bulletin, Scientific JournalЯзык: английский.Страна: Россия.Резюме или реферат: Diazotization of aminopyridines upon treatment with NaNO2 and H3PO4 in acetonitrile led to the formation of N-pyridinylacetamides. This reaction constitutes a convenient and general preparative method for the synthesis of 2-, 3-, and 4-N-pyridinylacetamides under mild conditions in good yields. The in situ oxidation of the thus obtained N-pyridinylacetamides with hydrogen peroxide gave good yields of pyridinylacetamide N-oxides..Примечания о наличии в документе библиографии/указателя: [References: p. 2314 (18 tit.)].Аудитория: .Тематика: электронный ресурс | труды учёных ТПУ | aminopyridines | diazotization | N-pyridinylacetamides | oxidation | аминопиридины | диазотирование | окисление Ресурсы он-лайн:Щелкните здесь для доступа в онлайнНет реальных экземпляров для этой записи
Title screen
[References: p. 2314 (18 tit.)]
Diazotization of aminopyridines upon treatment with NaNO2 and H3PO4 in acetonitrile led to the formation of N-pyridinylacetamides. This reaction constitutes a convenient and general preparative method for the synthesis of 2-, 3-, and 4-N-pyridinylacetamides under mild conditions in good yields. The in situ oxidation of the thus obtained N-pyridinylacetamides with hydrogen peroxide gave good yields of pyridinylacetamide N-oxides.
Для данного заглавия нет комментариев.
Личный кабинет оставить комментарий.