Аннотация:
N-Acetonylation of 5(3)-(1H-tetrazol-1-yl)-3(5)-nitro-1H-pyrazole with bromoacetone in the presence of NaHCO3 at 60°C gave, along with expected isomeric N-acetonyl derivatives, a tricyclic product of the intramolecular electrophilic attack at the carbon atom of the tetrazole cycle.
Реферативные базы данных:
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
A. V. Kormanov, T. K. Shkineva, I. L. Dalinger, “Acetonylation of 5(3)-(1H-tetrazol-1-yl)-3(5)-nitro-1H-pyrazole”, Mendeleev Commun., 27:5 (2017), 462–463