Abstract:
A new, efficient reagent–TMSCl/alkyl nitrite–is proposed for the conversion of imines into oximino derivatives, precursors of some important 1,2-diamines.
Document Type:
Article
Language: English
Citation:
E. A. Mistryukov, Ya. Rozpravka, O. N. Sorokina, “A Novel Synthesis of Imino Oximes via α-Nitrosation of Schiff Bases”, Mendeleev Commun., 3:5 (1993), 205
Linking options:
https://www.mathnet.ru/eng/mendc5335
https://www.mathnet.ru/eng/mendc/v3/i5/p205
This publication is cited in the following 4 articles:
E. Abele, R. Abele, K. Rubina, E. Lukevics, “Quinoline Oximes: Synthesis, Reactions, and Biological Activity. (Review)”, Chem Heterocycl Compd, 41:2 (2005), 137
V. A. Glushkov, V. I. Karmanov, Yu. V. Shklyaev, “Symmetrical and Unsymmetrical Bis-1,1′-(3,4-dihydroisoquinolines)”, Chem Heterocycl Compd, 41:4 (2005), 475
Yu. V. Shklyaev, B. Ya. Syropyatov, V. S. Shklyaev, M. S. Gavrilov, E. S. Boronenkova, R. Z. Dautova, B. B. Aleksandrov, A. A. Gorbunov, “Synthesis and anticoagulant and antiarrhythmic activity of oximes of isoquinolyl-1-glyoxylic acid derivatives”, Pharm Chem J, 33:9 (1999), 467
E. A. MISTRYUKOV, Y. ROZPRAVKA, O. N. SOROKINA, “ChemInform Abstract: A Novel Synthesis of Imino Oximes via α‐Nitrosation of Schiff Bases.”, ChemInform, 25:15 (1994)
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