Journal article

Synthetic Routes to Aminotriamantanes, Topological Analogues of the Neuroprotector Memantine


Authors listFokin, AA; Merz, A; Fokina, NA; Schwertfeger, H; Liu, SL; Dahl, JEP; Carlson, RMK; Schreiner, PR

Publication year2009

Pages909-912

JournalSynthesis: Journal of Synthetic Organic Chemistry

Volume number2009

Issue number6

ISSN0039-7881

DOI Linkhttps://doi.org/10.1055/s-0028-1087979

PublisherThieme Publishing / Georg Thieme Verlag


Abstract

The amino derivatives of diamantane and triamantane, representing
close topological analogues of the neuroprotective drug Memantine®,
were prepared via amination of the respective carboxylic acids or
alcohols.




Citation Styles

Harvard Citation styleFokin, A., Merz, A., Fokina, N., Schwertfeger, H., Liu, S., Dahl, J., et al. (2009) Synthetic Routes to Aminotriamantanes, Topological Analogues of the Neuroprotector Memantine, Synthesis: Journal of Synthetic Organic Chemistry, 2009(6), pp. 909-912. https://doi.org/10.1055/s-0028-1087979

APA Citation styleFokin, A., Merz, A., Fokina, N., Schwertfeger, H., Liu, S., Dahl, J., Carlson, R., & Schreiner, P. (2009). Synthetic Routes to Aminotriamantanes, Topological Analogues of the Neuroprotector Memantine. Synthesis: Journal of Synthetic Organic Chemistry. 2009(6), 909-912. https://doi.org/10.1055/s-0028-1087979


Last updated on 2025-21-05 at 14:54