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This article is cited in 14 scientific papers (total 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. Levita, V. P. Krasnova, A. M. Demina, M. I. Kodessa, L. Sh. Sadretdinovaa, T. V. Matveevaa, V. A. Ol'shevskayab, V. N. Kalininb, O. N. Chupakhina, V. N. Charushina 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.
Citation:
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-closo-dodecaboranes via acylation with chiral acyl chlorides”, Mendeleev Commun., 14:6 (2004), 293–295
Linking options:
https://www.mathnet.ru/eng/mendc3916 https://www.mathnet.ru/eng/mendc/v14/i6/p293
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