G. L. Levit, V. P. Krasnov, A. M. Demin, M. I. Kodess, L. Sh. Sadretdinova, T. V. Matveeva, V. A. Ol'shevskaya, V. N. Kalinin, O. N. Chupakhin, V. N. Charushin, “Kinetic resolution of 1-methyl- and 1-phenyl-3-amino-1,2-dicarba-<i>closo</i>-dodecaboranes <i>via</i> acylation with chiral acyl chlorides”, Mendeleev Commun., 2004, Volume 14, Issue 6,Pages <nobr>293–295</nobr>

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Mendeleev Commun., 2004 Volume 14, Issue 6, Pages 293–295 (Mi mendc3916)

This article is cited in 14 papers

Kinetic resolution of 1-methyl- and 1-phenyl-3-amino-1,2-dicarba-closo-dodecaboranes via acylation with chiral acyl chlorides

G. L. Levit^a, V. P. Krasnov^a, A. M. Demin^a, M. I. Kodess^a, L. Sh. Sadretdinova^a, T. V. Matveeva^a, V. A. Ol'shevskaya^b, V. N. Kalinin^b, O. N. Chupakhin^a, V. N. Charushin^a

^a I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
^b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation

Abstract: A study of the kinetic resolution of racemic 1-substituted 3-amino-1,2-dicarba-closo-dodecaboranes by chiral acyl chlorides has shown that N-tosyl-(S)-prolyl and N-phthaloyl-(S)-alaninyl chlorides are more efficient resolving agents than (S)-naproxen chloride.

Language: English

DOI: 10.1070/MC2004v014n06ABEH002047

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