N,N-Dimethoxy-N-tert-alkylamines: new synthesis methods and the crystal structure of the precursor
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Elsevier Inc.
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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N,N-Dimethoxy-N-tert-alkylamines: new synthesis methods and the crystal structure of the precursor / V. G. Shtamburg [et al.] // Mendeleev Commun. – 2006. – Vol. 16, № 2. – P. 84-85.