Abstract
Under the methanolysis of N-methoxy-N-(1-pyridinium)amines salts 1a-c, nucleophilic substitution occurs at the nitrogen atom to form N,N-dimethoxyamines 2a,b; the crystal structure of precursor 1c has been studied.
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CITATION STYLE
APA
Shtamburg, V. G., Tsygankov, A. V., Klots, E. A., Fedyanin, I. V., Lyssenko, K. A., & Kostyanovsky, R. G. (2006). N,N-Dimethoxy-N-tert-alkylamines: New synthesis methods and the crystal structure of the precursor. Mendeleev Communications, 16(2), 84–85. https://doi.org/10.1070/MC2006v016n02ABEH002222
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