RUS  ENG
Полная версия
ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2022, том 32, выпуск 6, страницы 771–773 (Mi mendc794)

Эта публикация цитируется в 4 статьях

Communications

Synthesis of trialkyl semithioglycolurils from alkylthiourea-glyoxal cyclic adducts and dialkylureas

A. A. Galochkin, V. V. Baranov, N. G. Kolotyrkina, A. N. Kravchenko

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation


Аннотация: Condensation of 1-alkyl-4,5-dihydroxyimidazolidine-2-thiones (monoalkylthiourea-glyoxal cyclic adducts) with 1,3-dialkylureas affords novel 1,4,6-trialkylsemithio- glycolurils having non-substituted NH group linked to C=S function. Such compounds can be accessed in two-stage one-pot reaction sequence from alkylthioureas and glyoxal followed by treatment of the resulting adduct with 1,3-dialkylureas

Ключевые слова: 1,4,6-trialkylsemithioglycolurils, one-pot synthesis, 4,5-dihydroxyimidazolidin-2-ones, 4,5-dihydroxyimidazolidine-2- thiones, alkylthioureas, dialkylureas.

Язык публикации: английский

DOI: 10.1016/j.mencom.2022.11.021



© МИАН, 2025