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For examples of transition-metal-catalyzed asymmetric conjugate reductions of amides, esters, ketones, and nitroalkenes, see: a) U. Leutenegger, A. Madin, A. Pfaltz, Angew. Chem. 1989, 101, 61-62; Angew. Chem. Int. Ed. Engl. 1989, 28, 60; b) D. H. Appella, Y. Moritani, R. Shintani, E. M. Ferreira, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9473-9474; c) B. H. Lipshutz, J. M. Servesko, Angew. Chem. 2003, 115, 4937-4940; Angew. Chem. Int. Ed. 2003, 42, 4789-4792; d) C. Czekelius, E. M. Carreira, Angew. Chem. 2003, 115, 4941-4943; Angew. Chem. Int. Ed. 2003, 42, 4793-4795.
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For examples of transition-metal-catalyzed asymmetric conjugate reductions of amides, esters, ketones, and nitroalkenes, see: a) U. Leutenegger, A. Madin, A. Pfaltz, Angew. Chem. 1989, 101, 61-62; Angew. Chem. Int. Ed. Engl. 1989, 28, 60; b) D. H. Appella, Y. Moritani, R. Shintani, E. M. Ferreira, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9473-9474; c) B. H. Lipshutz, J. M. Servesko, Angew. Chem. 2003, 115, 4937-4940; Angew. Chem. Int. Ed. 2003, 42, 4789-4792; d) C. Czekelius, E. M. Carreira, Angew. Chem. 2003, 115, 4941-4943; Angew. Chem. Int. Ed. 2003, 42, 4793-4795.
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For examples of transition-metal-catalyzed asymmetric conjugate reductions of amides, esters, ketones, and nitroalkenes, see: a) U. Leutenegger, A. Madin, A. Pfaltz, Angew. Chem. 1989, 101, 61-62; Angew. Chem. Int. Ed. Engl. 1989, 28, 60; b) D. H. Appella, Y. Moritani, R. Shintani, E. M. Ferreira, S. L. Buchwald, J. Am. Chem. Soc. 1999, 121, 9473-9474; c) B. H. Lipshutz, J. M. Servesko, Angew. Chem. 2003, 115, 4937-4940; Angew. Chem. Int. Ed. 2003, 42, 4789-4792; d) C. Czekelius, E. M. Carreira, Angew. Chem. 2003, 115, 4941-4943; Angew. Chem. Int. Ed. 2003, 42, 4793-4795.
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