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(b) Börner, A.; Ward, J.; Ruth, W.; Holz, J.; Kless, A.; Heller, D.; Kagan, H. B. Tetrahedron 1994, 50, 10419.
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10. Achiral polyhydroxy phosphines have been synthesized preferentially by a P-C-coupling reaction. Their metal complexes were investigated for biomedical application: (a) Katti, K. V.; Gali, H.; Smith, C. J.; Berning, D. E. Acc. Chem. Res. 1999, 32, 9.
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24
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0009718749
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The name is derived from BASF AG
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11. The name is derived from BASF AG.
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25
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0002022909
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and references cited therein
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12. (a) Burk, M. J.; Gross, M. F.; Harper, T. G. P.; Kalberg, C. S.; Lee, J. R.; Martinez, J. P. Pure & Appl. Chem. 1996, 68, 37 and references cited therein.
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Martinez, J.P.6
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(b) Burk, M. J.; Bienewald, F.; Challenger, S.; Derrick, A.; Ramsden, J. A. J. Org. Chem. 1999, 64, 3290.
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Ramsden, J.A.5
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27
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0001296673
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13. RoPHOS ligands: Holz, J.; Quirmbach, M.; Schmidt, U.; Heller, D.; Stürmer, R.; Börner, A. J. Org. Chem. 1998, 63, 8031. PennPHOS ligands: Jiang, Q.; Xiao, D.; Zhang, Z.; Cao, P.; Zhang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 516 and references cited therein. CnrPHOS ligand: Marinetti, A.; Genêt, J.-P; Jus, S.; Blanc, D.; Ratovelomanana-Vidal, V. Chem. Eur. J. 1999, 5, 1160.
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Holz, J.1
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Stürmer, R.5
Börner, A.6
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28
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0033557426
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and references cited therein
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13. RoPHOS ligands: Holz, J.; Quirmbach, M.; Schmidt, U.; Heller, D.; Stürmer, R.; Börner, A. J. Org. Chem. 1998, 63, 8031. PennPHOS ligands: Jiang, Q.; Xiao, D.; Zhang, Z.; Cao, P.; Zhang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 516 and references cited therein. CnrPHOS ligand: Marinetti, A.; Genêt, J.-P; Jus, S.; Blanc, D.; Ratovelomanana-Vidal, V. Chem. Eur. J. 1999, 5, 1160.
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Angew. Chem., Int. Ed. Engl.
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Jiang, Q.1
Xiao, D.2
Zhang, Z.3
Cao, P.4
Zhang, X.5
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29
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0032947082
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13. RoPHOS ligands: Holz, J.; Quirmbach, M.; Schmidt, U.; Heller, D.; Stürmer, R.; Börner, A. J. Org. Chem. 1998, 63, 8031. PennPHOS ligands: Jiang, Q.; Xiao, D.; Zhang, Z.; Cao, P.; Zhang, X. Angew. Chem., Int. Ed. Engl. 1999, 38, 516 and references cited therein. CnrPHOS ligand: Marinetti, A.; Genêt, J.-P; Jus, S.; Blanc, D.; Ratovelomanana-Vidal, V. Chem. Eur. J. 1999, 5, 1160.
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Chem. Eur. J.
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Marinetti, A.1
Genêt, J.-P.2
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15. Marzi, M.; Minetti, P.; Misiti, D. Tetrahedron 1992, 48, 10127.
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Misiti, D.3
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35
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0031802328
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and references cited therein. However, this approach necessitates the removal of the additives after the reaction
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16. In some cases improvement of the efficiency of non-polar phosphine catalysts in water has been achieved by the reaction in micelles (Selke, R.; Holz, J.; Riepe, A.; Börner, A. Chem. Eur. J. 1998, 5, 769 and references cited therein). However, this approach necessitates the removal of the additives after the reaction.
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Selke, R.1
Holz, J.2
Riepe, A.3
Börner, A.4
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