Abstract:
It was shown for the first time that aliphatic aldoxime-O-sulfonic acids can be stabilised as ammonium or alkylammonium salts and can be used in diaziridinium synthesis with primary aliphatic amines or ammonia to give 1,3-dialkyldiaziridines and 3-alkyldiaziridines, respectively; the latter compounds have not been previously easily accessible.
Document Type:
Article
Language: English
Citation:
A. N. Mikhailyuk, V. Yu. Petukhova, N. N. Makhova, “3-Alkyldiaziridines and 1,3-dialkyldiaziridines from aliphatic aldoxime-O-sulfonic acid salts”, Mendeleev Commun., 7:2 (1997), 60–61
Linking options:
https://www.mathnet.ru/eng/mendc4782
https://www.mathnet.ru/eng/mendc/v7/i2/p60
This publication is cited in the following 7 articles:
Edgars Abele, Edmunds Lukevics, Patai's Chemistry of Functional Groups, 2010
N. N. Makhova, N. G. Kamalova, Yu. A. Strelenko, “Synthesis of the first representatives of 3-ethynyldiaziridines”, Mendeleev Commun., 11:6 (2001), 227–229
N. N. Makhova, A. N. Mikhailyuk, V. V. Kuznetsov, S. A. Kutepov, P. A. Belyakov, “Effective synthesis of 1,2-di-, 1,2,3-tri-, 1,2,3,3-tetraalkyldiaziridines and 1,5-diazabicyclo[3.1.0]hexanes”, Mendeleev Commun., 10:5 (2000), 182–185
N. N. Makhova, G. A. Karpov, A. N. Mikhailyuk, L. I. Khmel'nitskii, “N-Alkylation of diaziridines”, Mendeleev Commun., 9:3 (1999), 112–114
J. M. MATHEWS, S. R. BLACK, L. T. BURKA, “Disposition of butanal oxime in rat following oral, intravenous and dermal administration”, Xenobiotica, 28:8 (1998), 767
A. N. MIKHAILYUK, V. YU. PETUKHOVA, N. N. MAKHOVA, “ChemInform Abstract: 3‐Alkyldiaziridines and 1,3‐Dialkyldiaziridines from Aliphatic Aldoxime‐O‐sulfonic Acid Salts.”, ChemInform, 28:38 (1997)
Contact us: