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0011061591
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note
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14 Amounts of chiral poisons: 2.0 equiv for Al, 1.4 equiv for Rh, 20 equiv for Ru, 3.0 equiv for Ti, and 2.0 equiv for Ir.
-
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52
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The real catalyst has been suggested to be a mono- or dihydride species (X = H or Cl): (a) Chowdhury, R. L.; Bäckvall, J.-E. J. Chem. Soc., Chem. Commun. 1991, 1063. (b) Haack, K.-J.; Hashiguchi, S.; Fujii, A.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. Engl. 1997, 36, 285. (c) Noyori, R.; Hashiguchi, S. Acc. Chem. Res. 1997, 30, 97. (d) Abdur-Rashid, K.; Lough, A. J.; Morris, R. H. Organometallics 2000, 19, 2655. (e) Abdur-Rashid, K.; Faatz, M.; Lough, A. J.; Morris, R. H. J. Am. Chem. Soc. 2001, 123, 7473. (f) Hartmann, R.; Chen, P. Angew. Chem. Int. Ed. 2001, 40, 3581.
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The real catalyst has been suggested to be a mono- or dihydride species (X = H or Cl): (a) Chowdhury, R. L.; Bäckvall, J.-E. J. Chem. Soc., Chem. Commun. 1991, 1063. (b) Haack, K.-J.; Hashiguchi, S.; Fujii, A.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. Engl. 1997, 36, 285. (c) Noyori, R.; Hashiguchi, S. Acc. Chem. Res. 1997, 30, 97. (d) Abdur-Rashid, K.; Lough, A. J.; Morris, R. H. Organometallics 2000, 19, 2655. (e) Abdur-Rashid, K.; Faatz, M.; Lough, A. J.; Morris, R. H. J. Am. Chem. Soc. 2001, 123, 7473. (f) Hartmann, R.; Chen, P. Angew. Chem. Int. Ed. 2001, 40, 3581.
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0002123299
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The real catalyst has been suggested to be a mono- or dihydride species (X = H or Cl): (a) Chowdhury, R. L.; Bäckvall, J.-E. J. Chem. Soc., Chem. Commun. 1991, 1063. (b) Haack, K.-J.; Hashiguchi, S.; Fujii, A.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. Engl. 1997, 36, 285. (c) Noyori, R.; Hashiguchi, S. Acc. Chem. Res. 1997, 30, 97. (d) Abdur-Rashid, K.; Lough, A. J.; Morris, R. H. Organometallics 2000, 19, 2655. (e) Abdur-Rashid, K.; Faatz, M.; Lough, A. J.; Morris, R. H. J. Am. Chem. Soc. 2001, 123, 7473. (f) Hartmann, R.; Chen, P. Angew. Chem. Int. Ed. 2001, 40, 3581.
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0034226592
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The real catalyst has been suggested to be a mono- or dihydride species (X = H or Cl): (a) Chowdhury, R. L.; Bäckvall, J.-E. J. Chem. Soc., Chem. Commun. 1991, 1063. (b) Haack, K.-J.; Hashiguchi, S.; Fujii, A.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. Engl. 1997, 36, 285. (c) Noyori, R.; Hashiguchi, S. Acc. Chem. Res. 1997, 30, 97. (d) Abdur-Rashid, K.; Lough, A. J.; Morris, R. H. Organometallics 2000, 19, 2655. (e) Abdur-Rashid, K.; Faatz, M.; Lough, A. J.; Morris, R. H. J. Am. Chem. Soc. 2001, 123, 7473. (f) Hartmann, R.; Chen, P. Angew. Chem. Int. Ed. 2001, 40, 3581.
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Abdur-Rashid, K.1
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The real catalyst has been suggested to be a mono- or dihydride species (X = H or Cl): (a) Chowdhury, R. L.; Bäckvall, J.-E. J. Chem. Soc., Chem. Commun. 1991, 1063. (b) Haack, K.-J.; Hashiguchi, S.; Fujii, A.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. Engl. 1997, 36, 285. (c) Noyori, R.; Hashiguchi, S. Acc. Chem. Res. 1997, 30, 97. (d) Abdur-Rashid, K.; Lough, A. J.; Morris, R. H. Organometallics 2000, 19, 2655. (e) Abdur-Rashid, K.; Faatz, M.; Lough, A. J.; Morris, R. H. J. Am. Chem. Soc. 2001, 123, 7473. (f) Hartmann, R.; Chen, P. Angew. Chem. Int. Ed. 2001, 40, 3581.
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The real catalyst has been suggested to be a mono- or dihydride species (X = H or Cl): (a) Chowdhury, R. L.; Bäckvall, J.-E. J. Chem. Soc., Chem. Commun. 1991, 1063. (b) Haack, K.-J.; Hashiguchi, S.; Fujii, A.; Ikariya, T.; Noyori, R. Angew. Chem., Int. Ed. Engl. 1997, 36, 285. (c) Noyori, R.; Hashiguchi, S. Acc. Chem. Res. 1997, 30, 97. (d) Abdur-Rashid, K.; Lough, A. J.; Morris, R. H. Organometallics 2000, 19, 2655. (e) Abdur-Rashid, K.; Faatz, M.; Lough, A. J.; Morris, R. H. J. Am. Chem. Soc. 2001, 123, 7473. (f) Hartmann, R.; Chen, P. Angew. Chem. Int. Ed. 2001, 40, 3581.
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Hartmann, R.1
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BIPHEP [(2,2 -bis(diphenylphosphino)-1, 1 -biphenyl]: This ligand was also named BPBP, but contrarily to what was claimed in the publication, it was unsuccessfully synthesized to give instead the monophosphine derivative: (a) Uehara, A.; Bailar, J. C. Jr. J. Organomet. Chem. 1982, 239, 1. (b) Bennett, M. A.; Bhargava, S. K.; Griffiths, K. D.; Robertson, G.B. Angew. Chem., Int. Ed. Engl. 1987, 26, 260. (c) Desponds, O.; Schlosser, M. J. Organomet. Chem. 1996, 507, 257. (d) Desponds, O.; Schlosser, M. Tetrahedron Lett. 1996, 37, 47.
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BIPHEP [(2,2 -bis(diphenylphosphino)-1, 1 -biphenyl]: This ligand was also named BPBP, but contrarily to what was claimed in the publication, it was unsuccessfully synthesized to give instead the monophosphine derivative: (a) Uehara, A.; Bailar, J. C. Jr. J. Organomet. Chem. 1982, 239, 1. (b) Bennett, M. A.; Bhargava, S. K.; Griffiths, K. D.; Robertson, G.B. Angew. Chem., Int. Ed. Engl. 1987, 26, 260. (c) Desponds, O.; Schlosser, M. J. Organomet. Chem. 1996, 507, 257. (d) Desponds, O.; Schlosser, M. Tetrahedron Lett. 1996, 37, 47.
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BIPHEP [(2,2 -bis(diphenylphosphino)-1, 1 -biphenyl]: This ligand was also named BPBP, but contrarily to what was claimed in the publication, it was unsuccessfully synthesized to give instead the monophosphine derivative: (a) Uehara, A.; Bailar, J. C. Jr. J. Organomet. Chem. 1982, 239, 1. (b) Bennett, M. A.; Bhargava, S. K.; Griffiths, K. D.; Robertson, G.B. Angew. Chem., Int. Ed. Engl. 1987, 26, 260. (c) Desponds, O.; Schlosser, M. J. Organomet. Chem. 1996, 507, 257. (d) Desponds, O.; Schlosser, M. Tetrahedron Lett. 1996, 37, 47.
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BIPHEP [(2,2 -bis(diphenylphosphino)-1, 1 -biphenyl]: This ligand was also named BPBP, but contrarily to what was claimed in the publication, it was unsuccessfully synthesized to give instead the monophosphine derivative: (a) Uehara, A.; Bailar, J. C. Jr. J. Organomet. Chem. 1982, 239, 1. (b) Bennett, M. A.; Bhargava, S. K.; Griffiths, K. D.; Robertson, G.B. Angew. Chem., Int. Ed. Engl. 1987, 26, 260. (c) Desponds, O.; Schlosser, M. J. Organomet. Chem. 1996, 507, 257. (d) Desponds, O.; Schlosser, M. Tetrahedron Lett. 1996, 37, 47.
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