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2-symmetric chiral monodentate NHCs are commonly employed as catalysts (see ref 1), application of the corresponding metal-based complexes is relatively uncommon in enantioselective catalysis. See
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2-symmetric chiral monodentate NHCs are commonly employed as catalysts (see ref 1), application of the corresponding metal-based complexes is relatively uncommon in enantioselective catalysis. See: (a) Enders, D.; Gielen, H.; Runsink, J.; Breuer, K.; Brode, S.; Boehn, K. Eur. J. Inorg. Chem. 1998, 913-919.
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67249147182
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note
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See the Supporting Information for experimental details.
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0001304637
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The arylsilyltrifluoride reagents used in this study are based on previously reported procedures
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The arylsilyltrifluoride reagents used in this study are based on previously reported procedures: (a) Brook, M. A.; Neuy, A. J. Org. Chem. 1990, 55, 3609-3616.
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Alkenylsilyltrifluorides were prepared based on the same previously reported procedures used to access the corresponding aryl-based reagents (see ref 19), but in somewhat lower yields (27-81%).
-
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87
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34250705242
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For applications of chiral NHC-Cu and NHC-Ru complexes developed in these laboratories to target-oriented synthesis, see
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For applications of chiral NHC-Cu and NHC-Ru complexes developed in these laboratories to target-oriented synthesis, see: (a) Gillingham, D. G.; Hoveyda, A. H. Angew. Chem., Int. Ed. 2007, 46, 3860-3864.
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All spectroscopic data match those reported previously; see
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