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Mendeleev Communications, 2004, Volume 14, Issue 6, Pages 293–295
DOI: https://doi.org/10.1070/MC2004v014n06ABEH002047
(Mi mendc3916)
 

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.
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Document Type: Article
Language: English


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
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  • https://www.mathnet.ru/eng/mendc/v14/i6/p293
  • This publication is cited in the following 14 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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