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1
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53349112974
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Ed, G. Dyker, Wiley-VCH, New York
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a) B. M. Stoltz, D. C. Ebner in Handbook of C-H Transformation, Vol. 2 (Ed.: G. Dyker), Wiley-VCH, New York, 2005, pp. 393-401;
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Stoltz, B.M.1
Ebner, D.C.2
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5
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0038276940
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b) J. T. Bagdanoff, E. M. Ferreira, B. M. Stoltz, Org. Lett. 2003, 5, 835-837.
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Bagdanoff, J.T.1
Ferreira, E.M.2
Stoltz, B.M.3
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7
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0346500606
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Angew. Chem. Int. Ed. 2004, 43, 353-357.
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8
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0034823071
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Simultaneous with our report, a similar system was reported, see
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Simultaneous with our report, a similar system was reported, see: D. R. Jensen, J. S. Pugsley, M. S. Sigman, J. Am. Chem. Soc. 2001, 123, 7475-7476.
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J. Am. Chem. Soc
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Jensen, D.R.1
Pugsley, J.S.2
Sigman, M.S.3
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9
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1942535137
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For some synthetic applications, see: a
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For some synthetic applications, see: a) D. D. Caspi, D. C. Ebner, J. T. Bagdanoff, B. M. Stoltz, Adv. Synth. Catal. 2004, 346, 185-189;
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(2004)
Adv. Synth. Catal
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Caspi, D.D.1
Ebner, D.C.2
Bagdanoff, J.T.3
Stoltz, B.M.4
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11
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85050296727
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For discussions of kinetic resolution, see: a, Ed, E. L. Eliel, Wiley, New York
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For discussions of kinetic resolution, see: a) H. B. Kagan, J. C. Fiaud in Topics in Stereochemistry, Vol. 18 (Ed.: E. L. Eliel), Wiley, New York, 1988, pp. 249-330;
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(1988)
Topics in Stereochemistry
, vol.18
, pp. 249-330
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Kagan, H.B.1
Fiaud, J.C.2
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12
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0002178750
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b) J. M. Keith, J. F. Larrow, E. N. Jacobsen, Adv. Synth. Catal. 2001, 343, 5-26;
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Adv. Synth. Catal
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Keith, J.M.1
Larrow, J.F.2
Jacobsen, E.N.3
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14
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21344465658
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Angew. Chem. Int. Ed. 2005, 44, 3974-4001.
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15
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0037986275
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For examples with alternative ligands in the palladium-catalyzed oxidative kinetic resolution of secondary alcohols, see: a D. R. Jensen, M. S. Sigman, Org. Lett. 2003, 5, 63-65;
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For examples with alternative ligands in the palladium-catalyzed oxidative kinetic resolution of secondary alcohols, see: a) D. R. Jensen, M. S. Sigman, Org. Lett. 2003, 5, 63-65;
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16
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33947147700
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b) T. Chen, J.-J. Jiang, Q. Xu, M. Shi, Org. Lett. 2007, 9, 865-868.
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Chen, T.1
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Xu, Q.3
Shi, M.4
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18
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3042643476
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R. J. Nielsen, J. M. Keith, B. M. Stoltz, W. A. Goddard III, J. Am. Chem. Soc. 2004, 126, 7967-7974.
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Nielsen, R.J.1
Keith, J.M.2
Stoltz, B.M.3
Goddard III, W.A.4
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19
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53349158615
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See the Supporting Information for details
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See the Supporting Information for details.
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-
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20
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53349110892
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3> I> OAc, see the Supporting Information for details.
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3> I> OAc, see the Supporting Information for details.
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22
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53349139829
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274539 for 12, and 639648 for 13 contain the supplementary crystallographic data for this paper
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CCDC 298214 for 6
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CCDC 298214 for 6, 274539 for 12, and 639648 for 13 contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
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These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
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23
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53349169585
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2] as the catalyst, see the Supporting Information for details.
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2] as the catalyst, see the Supporting Information for details.
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-
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24
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53349105372
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slow = ln[(1-C)(1-ee)]/ln[(1- C)(1+ee)], where C is conversion, see: reference [6a].
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slow = ln[(1-C)(1-ee)]/ln[(1- C)(1+ee)], where C is conversion, see: reference [6a].
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25
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53349158614
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2 sources, see the Supporting Information for details.
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2 sources, see the Supporting Information for details.
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26
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0001147659
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For an asymmetric synthesis of, -sparteine, see
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For an asymmetric synthesis of (+)-sparteine, see: B. T. Smith, J. A. Wendt, J. Aubé, Org. Lett. 2002, 4, 2577-2579.
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Smith, B.T.1
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Aubé, J.3
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27
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0037048610
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28
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4043120293
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85026879940
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A. J. Dixon, M. J. McGrath, P. O'Brien, Org. Synth. 2006, 83, 141-154.
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Dixon, A.J.1
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33748480130
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U. K. Tambar, D. C. Ebner, B. M. Stoltz, J. Am. Chem. Soc. 2006, 128, 11752-11753.
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Tambar, U.K.1
Ebner, D.C.2
Stoltz, B.M.3
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