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For pertinent works concerning P-chiral monophosphines with a nitrogen chelating group, see: (a) Yang, H.; Alvarez, M.; Lugan, N.; Mathieu, R. J. Chem. Soc., Chem. Commun. 1995, 1721-1722. (b) Kudis, S.; Helmchen, G. Angew. Chem., Int. Ed. 1998, 37, 3047-3050. (c) Helmchen, G.; Kudis, S.; Sennhenn, P.; Steinhagen, H. Pure Appl. Chem. 1997, 513-519.
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For chirostructural analysis of the chelate/transition metal ring precatalyst, see: (a) Ref. Id, pages 47-50. (b) Brunner, H.; Winter, A.; Breu, J. J. Organomet. Chem. 1998, 553, 285-306. (c) RajanBabu, T. V.; Radetich, B.; You, K. K.; Casalnuovo, A. L.; Calabrese, J. C. J. Org. Chem. 1999, 64, 3429-3447, and references cited therein.
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44
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For chirostructural analysis of the chelate/transition metal ring precatalyst, see: (a) Ref. Id, pages 47-50. (b) Brunner, H.; Winter, A.; Breu, J. J. Organomet. Chem. 1998, 553, 285-306. (c) RajanBabu, T. V.; Radetich, B.; You, K. K.; Casalnuovo, A. L.; Calabrese, J. C. J. Org. Chem. 1999, 64, 3429-3447, and references cited therein.
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and references cited therein
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For chirostructural analysis of the chelate/transition metal ring precatalyst, see: (a) Ref. Id, pages 47-50. (b) Brunner, H.; Winter, A.; Breu, J. J. Organomet. Chem. 1998, 553, 285-306. (c) RajanBabu, T. V.; Radetich, B.; You, K. K.; Casalnuovo, A. L.; Calabrese, J. C. J. Org. Chem. 1999, 64, 3429-3447, and references cited therein.
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0342479871
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Institut für Technische Chemie und Petrolchemie, Aachen, Germany, communication July, Göetingen, and private communication
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The synthesis and studies of P-chiral aminophosphine phosphinite ligands, applied in asymmetric catalysis for hydroformylation are in progress: Ewalds, R.; Vogt, D. (Institut für Technische Chemie und Petrolchemie, Aachen, Germany), communication at 9th IUPAC Symposium on OMCOS 1997, July, Göetingen, and private communication.
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48
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0342479870
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HC1 acidolysis of aminophosphines 2a (or 2b), leads to chlorophosphine boranes 3a (or 3b) with inversion of configuration: (a) Ref. 7f. (b) Moulin, D. PhD thesis, 1999, Cergy-Pontoise
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HC1 acidolysis of aminophosphines 2a (or 2b), leads to chlorophosphine boranes 3a (or 3b) with inversion of configuration: (a) Ref. 7f. (b) Moulin, D. PhD thesis, 1999, Cergy-Pontoise.
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49
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0343349305
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note
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Asymmetric hydrogenation of subtrate 6 using (+)-PPHOS 5a′-Rh complex in benzene, have been reported to give the aminoester 7 in 82% e.e. by Pracejus and colleagues (Ref. 3b).
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