Abstract:
The reactions of 1,3,5-trialkylhexahydro-1,3,5-triazines with N-chloroalkylamines resulted in 1,2-dialkyldiaziridines, whereas the reactions of N-chloroalkylamines or N,N-dichloroalkylamines with an excess of primary aliphatic amines gave 1,2,3-trialkyldiaziridines.
Document Type:
Article
Language: English
Citation:
V. V. Kuznetsov, N. N. Makhova, D. E. Dmitriev, V. V. Seregin, “Syntheses of 1,2-di- and 1,2,3-trialkyldiaziridines”, Mendeleev Commun., 15:3 (2005), 116–118
Linking options:
https://www.mathnet.ru/eng/mendc3702
https://www.mathnet.ru/eng/mendc/v15/i3/p116
This publication is cited in the following 4 articles:
V. V. Kuznetsov, V. V. Seregin, D. V. Khakimov, T. S. Pivina, M. D. Vedenyapina, A. A. Vedenyapin, N. N. Makhova, “The study of the formation mechanism of 1,2,3-trialkyldiaziridines by kinetic and quantum chemistry methods”, Russ Chem Bull, 63:9 (2014), 2000
Vera Yu. Petukhova, Leonid L. Fershtat, Vadim V. Kachala, Vladimir V. Kuznetsov, Dmitriy V. Khakimov, Tatyana S. Pivina, Nina N. Makhova, “Reaction of 1,2‐Dialkyldiaziridines and 1,2,3‐Trialkyldiaziridines with Methyl Propiolate in Ionic Liquids and in Organic Solvents”, Journal of Heterocyclic Chem, 50:2 (2013), 326
Vladimir V. Kuznetsov, Nina N. Makhova, Dmitrii E. Dmitriev, Victor V. Seregin, “Syntheses of 1,2‐Di‐ and 1,2,3‐Trialkyldiaziridines.”, ChemInform, 36:39 (2005)
Contact us: