Abstract
New secondary-tertiary diamines were prepared from elatidal imines with primary amino alcohols, derivatives of natural amino acids of the S-series. N-Methylation of the diamines yielded bi-tertiary diamines unable to undergo quaternization with MeI due to steric hindrance.
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Ganbaatar, J., Osadchii, S.A., Shults, E.E. et al. Study of alkaloids of the Siberian and Altai flora. 9. Synthesis of amino derivatives of elatidine. Russian Chemical Bulletin 51, 2290–2294 (2002). https://doi.org/10.1023/A:1022103922923
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DOI: https://doi.org/10.1023/A:1022103922923