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The enantiomerically pure (S, S)-5 and its enantiomer (R, R)-5 (>99% ee) were obtained through the lipase-catalyzed kinetic resolution of rac-5 following the literature procedure, see: (a) Lemke, K.; Ballschuh, S.; Kunath, A.; Theil, F. Tetrahedron: Asymmetry 1997, 8, 2051.
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The enantiomerically pure (S, S)-5 and its enantiomer (R, R)-5 (>99% ee) were obtained through the lipase-catalyzed kinetic resolution of rac-5 following the literature procedure, see: (a) Lemke, K.; Ballschuh, S.; Kunath, A.; Theil, F. Tetrahedron: Asymmetry 1997, 8, 2051.
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For other recent examples of asymmetric synthesis of diarylmethylamines, see: a
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For other recent examples of asymmetric synthesis of diarylmethylamines, see: (a) Hayashi, T.; Kawai, M.; Tokunaga, N. Angew. Chem., Int. Ed. 2004, 43, 6125.
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Only a limited number of examples were given by the asymmetric reaction of N-tosylarylimines with arylboroxines see ref 2c and 6a
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Only a limited number of examples were given by the asymmetric reaction of N-tosylarylimines with arylboroxines (see ref 2c and 6a).
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For recent chiral auxiliary-mediated asymmetric synthesis, see: a
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For recent chiral auxiliary-mediated asymmetric synthesis, see: (a) Comins, D. L.; Schilling, S.; Zhang, Y. Org. Lett. 2005, 7, 95.
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For a review, see: Stajer, G.; Csende, F. Curr. Org. Chem. 2005, 9, 1277.
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In the cases of asymmetric arylation of N-tosylarylimines using Hayashi's chiral diene ligand and Tomioka's chiral amidomonophosphane ligand, arylboroxines were used see ref 2c and 6a
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In the cases of asymmetric arylation of N-tosylarylimines using Hayashi's chiral diene ligand and Tomioka's chiral amidomonophosphane ligand, arylboroxines were used (see ref 2c and 6a).
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