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79957486501
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Reviews
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Reviews:
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5
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0038634036
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A. Pfaltz, J. Blankenstein, R. Hilgraf, E. Hörmann, S. McIntyre, F. Menges, M. Schönleber, S.P. Smidt, B. Wüstenberg, and N. Zimmermann Adv. Synth. Catal. 345 2003 33 43
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(2003)
Adv. Synth. Catal.
, vol.345
, pp. 33-43
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Pfaltz, A.1
Blankenstein, J.2
Hilgraf, R.3
Hörmann, E.4
McIntyre, S.5
Menges, F.6
Schönleber, M.7
Smidt, S.P.8
Wüstenberg, B.9
Zimmermann, N.10
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6
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79957502121
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Selected, recent examples
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Selected, recent examples:
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7
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77954290900
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J.J. Verendel, T. Zhou, J.-Q. Li, A. Paptchikhine, O. Lebedev, and P.G. Andersson J. Am. Chem. Soc. 132 2010 8880 8881
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(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 8880-8881
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Verendel, J.J.1
Zhou, T.2
Li, J.-Q.3
Paptchikhine, A.4
Lebedev, O.5
Andersson, P.G.6
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13
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69349089064
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J. Mazuela, J.J. Verendel, M. Coll, B. Schäffner, A. Börner, P.G. Andersson, O. Pmies, and M. Diéguez J. Am. Chem. Soc. 131 2009 12344 12353
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(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 12344-12353
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Mazuela, J.1
Verendel, J.J.2
Coll, M.3
Schäffner, B.4
Börner, A.5
Andersson, P.G.6
Pmies, O.7
Diéguez, M.8
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18
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44949222632
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M. Diéguez, J. Mazuela, O. Pmies, J.J. Verendel, and P.G. Andersson J. Am. Chem. Soc. 130 2008 7208 7209
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(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 7208-7209
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Diéguez, M.1
Mazuela, J.2
Pmies, O.3
Verendel, J.J.4
Andersson, P.G.5
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22
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50249096226
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M. Diéguez, J. Mazuela, O. Pmies, J.J. Verendel, and P.G. Andersson Chem. Commun. 2008 3888 3890
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(2008)
Chem. Commun.
, pp. 3888-3890
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Diéguez, M.1
Mazuela, J.2
Pmies, O.3
Verendel, J.J.4
Andersson, P.G.5
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28
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0029993806
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Helmchen and coworkers synthesized ligand 7 and the related THP ether: M. Peer, J.C. de Jong, M. Kiefer, T. Langer, H. Rieck, H. Schell, P. Sennhenn, J. Sprinz, H. Steinhagen, B. Wiese, and G. Helmchen Tetrahedron 52 1996 7547 7583
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(1996)
Tetrahedron
, vol.52
, pp. 7547-7583
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Peer, M.1
De Jong, J.C.2
Kiefer, M.3
Langer, T.4
Rieck, H.5
Schell, H.6
Sennhenn, P.7
Sprinz, J.8
Steinhagen, H.9
Wiese, B.10
Helmchen, G.11
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29
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79957504471
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Ligand 10 and the corresponding TBDMS ether were reported by Stoltz and coworkers. In a palladium-catalyzed enantioselective decarboxylative protonation the TBDMS derivative was found to be inferior to the tert-butyl phosphinooxazoline ligand
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Ligand 10 and the corresponding TBDMS ether were reported by Stoltz and coworkers. In a palladium-catalyzed enantioselective decarboxylative protonation the TBDMS derivative was found to be inferior to the tert-butyl phosphinooxazoline ligand:
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33
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79957452086
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Stohler, R. Ph.D. Thesis, University of Basel, 2006
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Stohler, R. Ph.D. Thesis, University of Basel, 2006.
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34
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79957456517
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For reaction conditions and additional asymmetric hydrogenation experiments see the Supplementary data
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For reaction conditions and additional asymmetric hydrogenation experiments see the Supplementary data.
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35
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79957532524
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int=0.00), 29,618 used in all calculations. The final wR was 0.0500 (all data). For a selection of bond lengths and angles see the supplementary data. Crystallographic data (excluding structure factors) for 31 have been deposited with the Cambridge Crystallographic Data Center as supplementary publication no. CCDC-805973. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: +44 1223 336033 or e-mail
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int=0.00), 29,618 used in all calculations. The final wR was 0.0500 (all data). For a selection of bond lengths and angles see the supplementary data. Crystallographic data (excluding structure factors) for 31 have been deposited with the Cambridge Crystallographic Data Center as supplementary publication no. CCDC-805973. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (fax: +44 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk ).
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37
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4244085862
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M.A. Esteruelas, M.P. García, F.J. Lahoz, M. Martín, J. Modrego, E. Oñate, and L.A. Oro Inorg. Chem. 33 1994 3473 3480
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(1994)
Inorg. Chem.
, vol.33
, pp. 3473-3480
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Esteruelas, M.A.1
García, M.P.2
Lahoz, F.J.3
Martín, M.4
Modrego, J.5
Oñate, E.6
Oro, L.A.7
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40
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0037416257
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S.P. Smidt, A. Pfaltz, E. Martínez-Viviente, P.S. Pregosin, and A. Albinati Organometallics 22 2003 1000 1009
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(2003)
Organometallics
, vol.22
, pp. 1000-1009
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Smidt, S.P.1
Pfaltz, A.2
Martínez-Viviente, E.3
Pregosin, P.S.4
Albinati, A.5
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41
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79957517430
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For details of the X-ray crystallograhic investigations see the Supplementary data
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For details of the X-ray crystallograhic investigations see the Supplementary data.
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43
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0035898080
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D.L. Reger, T.D. Wright, C.A. Little, J.J.S. Lamba, and M.D. Smith Inorg. Chem. 40 2001 3810 3814
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(2001)
Inorg. Chem.
, vol.40
, pp. 3810-3814
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Reger, D.L.1
Wright, T.D.2
Little, C.A.3
Lamba, J.J.S.4
Smith, M.D.5
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46
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79957469547
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13C) ppm, respectively, were used to calibrate the spectra
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13C) ppm, respectively, were used to calibrate the spectra.
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49
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0030944755
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P. Schnider, G. Koch, R. Prétôt, G. Wang, F.M. Bohnen, C. Krüger, and A. Pfaltz Chem. - Eur. J. 3 1997 887 892
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(1997)
Chem. - Eur. J.
, vol.3
, pp. 887-892
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Schnider, P.1
Koch, G.2
Prétôt, R.3
Wang, G.4
Bohnen, F.M.5
Krüger, C.6
Pfaltz, A.7
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50
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79957534055
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R 14.2 (product) and 16.1 (substrate) min
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R 14.2 (product) and 16.1 (substrate) min.
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