Journalartikel

Jahr der Veröffentlichung: 2007

Seiten: 4738-4745

Zeitschrift: European Journal of Organic Chemistry

Bandnummer: 2007

Heftnummer: 28

DOI Link: https://doi.org/10.1002/ejoc.200700378

Verlag: Wiley

Abstract: 

Functionalizations of diamantane, triamantane, and tetramantane with electrophilic reagents (Br₂,
nitric acid) lead to various apical and medial disubstituted products
that were separated and characterized individually. The highly desirable
and otherwise inaccessible thermodynamically more stable apical
bis‐derivatives were obtained with high preparative yields through acid
catalyzed isomerizations.

Harvard-Zitierstil: Fokina, N., Tkachenko, B., Merz, A., Serafin, M., Dahl, J., Carlson, R., et al. (2007) Hydroxy Derivatives of Diamantane, Triamantane, and [121]Tetramantane: Selective Preparation of Bis‐Apical Derivatives, European Journal of Organic Chemistry, 2007(28), pp. 4738-4745. https://doi.org/10.1002/ejoc.200700378

APA-Zitierstil: Fokina, N., Tkachenko, B., Merz, A., Serafin, M., Dahl, J., Carlson, R., Fokin, A., & Schreiner, P. (2007). Hydroxy Derivatives of Diamantane, Triamantane, and [121]Tetramantane: Selective Preparation of Bis‐Apical Derivatives. European Journal of Organic Chemistry. 2007(28), 4738-4745. https://doi.org/10.1002/ejoc.200700378