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Selected examples for peptide-based modular ligands: a) M. S. Sigman, E. N. Jacobsen, J. Am. Chem. Soc. 1998, 120, 4901; b) S. R. Gilbertson, X. Wang, Tetrahedron Lett. 1996, 37, 6457; B. M. Cole, K. D. Shimizu, B. M. Cole, C. A. Krueger, K. W. Kuntz, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 1997, 109, 1782; C. A. Luchaco-Cullis, H. Mizutani, K. E. Murphy, A. H. Hoveyda, Angew. Chem. 2001, 113, 1504; Angew. Chem. Int. Ed. 2001, 40, 1456; e) S. J. Degrado, H. Mizutani, A. H. Hoveyda, J. Am. Chem. Soc. 2001, 123, 755; and refs. cited therein.
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Selected examples for peptide-based modular ligands: a) M. S. Sigman, E. N. Jacobsen, J. Am. Chem. Soc. 1998, 120, 4901; b) S. R. Gilbertson, X. Wang, Tetrahedron Lett. 1996, 37, 6457; B. M. Cole, K. D. Shimizu, B. M. Cole, C. A. Krueger, K. W. Kuntz, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 1997, 109, 1782; C. A. Luchaco-Cullis, H. Mizutani, K. E. Murphy, A. H. Hoveyda, Angew. Chem. 2001, 113, 1504; Angew. Chem. Int. Ed. 2001, 40, 1456; e) S. J. Degrado, H. Mizutani, A. H. Hoveyda, J. Am. Chem. Soc. 2001, 123, 755; and refs. cited therein.
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Selected examples for peptide-based modular ligands: a) M. S. Sigman, E. N. Jacobsen, J. Am. Chem. Soc. 1998, 120, 4901; b) S. R. Gilbertson, X. Wang, Tetrahedron Lett. 1996, 37, 6457; B. M. Cole, K. D. Shimizu, B. M. Cole, C. A. Krueger, K. W. Kuntz, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 1997, 109, 1782; d) C. A. Luchaco-Cullis, H. Mizutani, K. E. Murphy, A. H. Hoveyda, Angew. Chem. 2001, 113, 1504; Angew. Chem. Int. Ed. 2001, 40, 1456; e) S. J. Degrado, H. Mizutani, A. H. Hoveyda, J. Am. Chem. Soc. 2001, 123, 755; and refs. cited therein.
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Selected examples for peptide-based modular ligands: a) M. S. Sigman, E. N. Jacobsen, J. Am. Chem. Soc. 1998, 120, 4901; b) S. R. Gilbertson, X. Wang, Tetrahedron Lett. 1996, 37, 6457; B. M. Cole, K. D. Shimizu, B. M. Cole, C. A. Krueger, K. W. Kuntz, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 1997, 109, 1782; C. A. Luchaco-Cullis, H. Mizutani, K. E. Murphy, A. H. Hoveyda, Angew. Chem. 2001, 113, 1504; Angew. Chem. Int. Ed. 2001, 40, 1456; e) S. J. Degrado, H. Mizutani, A. H. Hoveyda, J. Am. Chem. Soc. 2001, 123, 755; and refs. cited therein.
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11
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and refs. cited therein
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Selected examples for peptide-based modular ligands: a) M. S. Sigman, E. N. Jacobsen, J. Am. Chem. Soc. 1998, 120, 4901; b) S. R. Gilbertson, X. Wang, Tetrahedron Lett. 1996, 37, 6457; B. M. Cole, K. D. Shimizu, B. M. Cole, C. A. Krueger, K. W. Kuntz, M. L. Snapper, A. H. Hoveyda, Angew. Chem. 1997, 109, 1782; C. A. Luchaco-Cullis, H. Mizutani, K. E. Murphy, A. H. Hoveyda, Angew. Chem. 2001, 113, 1504; Angew. Chem. Int. Ed. 2001, 40, 1456; e) S. J. Degrado, H. Mizutani, A. H. Hoveyda, J. Am. Chem. Soc. 2001, 123, 755; and refs. cited therein.
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for a very recent contribution, see
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d) G. J. Dawson, C. G. Frost, J. M. J. Williams, S. J. Coote, Tetrahedron Lett. 1993, 34, 3149; for a very recent contribution, see,
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24
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For other recent examples of tunable modular ligands, see: a) H. Park, T. V. RajanBaBu, J. Am. Chem. Soc. 2002, 124, 734; b) J. Blankenstein, A. Pfaltz, Angew. Chem. Int. Ed. 2001, 40, 4445; c) P. G. Cozzi, N. Zimmermann, R. Hilgraf, S. Schaffner, A. Pfaltz, Adv. Synth. Catal. 2001, 343, 450; d) M. J. Burk, Acc. Chem. Res. 2000, 33, 363; e) S. Ongeri, U. Piarulli, R. F. W. Jackson, C. Gennari, Eur. J. Org. Chem. 2001, 803; f) S. R. Gilbertson, C.-W. T. Chang, J. Org. Chem. 1998, 63, 8424.
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Park, H.1
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0035803746
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For other recent examples of tunable modular ligands, see: a) H. Park, T. V. RajanBaBu, J. Am. Chem. Soc. 2002, 124, 734; b) J. Blankenstein, A. Pfaltz, Angew. Chem. Int. Ed. 2001, 40, 4445; c) P. G. Cozzi, N. Zimmermann, R. Hilgraf, S. Schaffner, A. Pfaltz, Adv. Synth. Catal. 2001, 343, 450; d) M. J. Burk, Acc. Chem. Res. 2000, 33, 363; e) S. Ongeri, U. Piarulli, R. F. W. Jackson, C. Gennari, Eur. J. Org. Chem. 2001, 803; f) S. R. Gilbertson, C.-W. T. Chang, J. Org. Chem. 1998, 63, 8424.
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Pfaltz, A.2
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26
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0001596428
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For other recent examples of tunable modular ligands, see: a) H. Park, T. V. RajanBaBu, J. Am. Chem. Soc. 2002, 124, 734; b) J. Blankenstein, A. Pfaltz, Angew. Chem. Int. Ed. 2001, 40, 4445; c) P. G. Cozzi, N. Zimmermann, R. Hilgraf, S. Schaffner, A. Pfaltz, Adv. Synth. Catal. 2001, 343, 450; d) M. J. Burk, Acc. Chem. Res. 2000, 33, 363; e) S. Ongeri, U. Piarulli, R. F. W. Jackson, C. Gennari, Eur. J. Org. Chem. 2001, 803; f) S. R. Gilbertson, C.-W. T. Chang, J. Org. Chem. 1998, 63, 8424.
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Cozzi, P.G.1
Zimmermann, N.2
Hilgraf, R.3
Schaffner, S.4
Pfaltz, A.5
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27
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0033918708
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For other recent examples of tunable modular ligands, see: a) H. Park, T. V. RajanBaBu, J. Am. Chem. Soc. 2002, 124, 734; b) J. Blankenstein, A. Pfaltz, Angew. Chem. Int. Ed. 2001, 40, 4445; c) P. G. Cozzi, N. Zimmermann, R. Hilgraf, S. Schaffner, A. Pfaltz, Adv. Synth. Catal. 2001, 343, 450; d) M. J. Burk, Acc. Chem. Res. 2000, 33, 363; e) S. Ongeri, U. Piarulli, R. F. W. Jackson, C. Gennari, Eur. J. Org. Chem. 2001, 803; f) S. R. Gilbertson, C.-W. T. Chang, J. Org. Chem. 1998, 63, 8424.
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For other recent examples of tunable modular ligands, see: a) H. Park, T. V. RajanBaBu, J. Am. Chem. Soc. 2002, 124, 734; b) J. Blankenstein, A. Pfaltz, Angew. Chem. Int. Ed. 2001, 40, 4445; c) P. G. Cozzi, N. Zimmermann, R. Hilgraf, S. Schaffner, A. Pfaltz, Adv. Synth. Catal. 2001, 343, 450; d) M. J. Burk, Acc. Chem. Res. 2000, 33, 363; e) S. Ongeri, U. Piarulli, R. F. W. Jackson, C. Gennari, Eur. J. Org. Chem. 2001, 803; f) S. R. Gilbertson, C.-W. T. Chang, J. Org. Chem. 1998, 63, 8424.
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For other recent examples of tunable modular ligands, see: a) H. Park, T. V. RajanBaBu, J. Am. Chem. Soc. 2002, 124, 734; b) J. Blankenstein, A. Pfaltz, Angew. Chem. Int. Ed. 2001, 40, 4445; c) P. G. Cozzi, N. Zimmermann, R. Hilgraf, S. Schaffner, A. Pfaltz, Adv. Synth. Catal. 2001, 343, 450; d) M. J. Burk, Acc. Chem. Res. 2000, 33, 363; e) S. Ongeri, U. Piarulli, R. F. W. Jackson, C. Gennari, Eur. J. Org. Chem. 2001, 803; f) S. R. Gilbertson, C.-W. T. Chang, J. Org. Chem. 1998, 63, 8424.
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Examples for the synthesis of ClP(III)-electrophiles from diols: a) M. J. Baker, P. G. Pringel, J. Chem. Soc. Chem. Commun. 1991, 1292; b) N. Greene, T. P. Kee, Synth. Commun. 1993, 23, 1651; c) M. T. Reetz, T. Neugebauer, Angew. Chem. 1999, 111, 134.
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Examples for the synthesis of ClP(III)-electrophiles from diols: a) M. J. Baker, P. G. Pringel, J. Chem. Soc. Chem. Commun. 1991, 1292; b) N. Greene, T. P. Kee, Synth. Commun. 1993, 23, 1651; c) M. T. Reetz, T. Neugebauer, Angew. Chem. 1999, 111, 134.
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For a comprehensive review, see: a) N. Miyaura, A. Suzuki, Chem. Rev. 1995, 95, 2457; for the combination of ortho-metallation/Suzuki-coupling, see: b) M. J. Sharp, W. Cheng, V. Snieckus, Tetrahedron Lett. 1987, 43, 5093.
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For a comprehensive review, see: a) N. Miyaura, A. Suzuki, Chem. Rev. 1995, 95, 2457; for the combination of ortho-metallation/Suzuki-coupling, see: b) M. J. Sharp, W. Cheng, V. Snieckus, Tetrahedron Lett. 1987, 43, 5093.
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36
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0348059688
-
-
note
-
The commercially obtained dark solid was purified by flash-chromatography (hexane/EtOAc, 2:1) to give 24 as a white crystalline compound.
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38
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33845183513
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b) T. Hayashi, Y. Matsumoto, Y. Ito, J. Am. Chem. Soc. 1989, 111, 3426;
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for a review with references up to 1996, see: d) T. Hayashi, in: Comprehensive Asymmetric Catalysis, Vol. I (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Berlin-Heidelberg, 1999, p. 351;
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Hayashi, T.1
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0346852349
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for selected recent work, see: e) S. Demay, F. Volant, P. Knochel, Angew. Chem. 2001, 113, 1272; Angew. Chem. Int. Ed. 2001, 40, 1235;
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42
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for selected recent work, see: e) S. Demay, F. Volant, P. Knochel, Angew. Chem. 2001, 113, 1272; Angew. Chem. Int. Ed. 2001, 40, 1235;
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43
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and refs. cited therein
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f) F. Y. Kwong, Q. Yang, T. C. W. Mak, A. S. Chan, K. S. Chan, J. Org. Chem. 2002, 67, 2769 and refs. cited therein.
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44
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0034660158
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[12f] as well as: a) E. Fernandez, K. Maeda, M. W. Hooper, J. M. Brown Chem. Enr. J. 2000, 6, 1840; b) M. McCarthy, M. W. Hooper, P. J. Guiry, Chem. Commun. 2000, 1333.
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45
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0034698223
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[12f] as well as: a) E. Fernandez, K. Maeda, M. W. Hooper, J. M. Brown Chem. Enr. J. 2000, 6, 1840; b) M. McCarthy, M. W. Hooper, P. J. Guiry, Chem. Commun. 2000, 1333.
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46
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48
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0035888802
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While this work was in progress, somewhat related phosphine-phosphite ligands (prepared by a different route) were reported to give high enantioselectivities in catalytic hydrogenations, see: A. Suarez, A. Pizzano, Tetrahedron: Asymmetry 2001, 12, 2501.
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E. Vedejs, D. A. Engler, J. E. Telschow, J. Org. Chem. 1978, 43, 188.
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