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Эта публикация цитируется в 14 научных статьях (всего в 14 статьях)
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
Аннотация:
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.
Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3916 https://www.mathnet.ru/rus/mendc/v14/i6/p293
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