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1
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0003400107
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John Wiley and Sons Ltd., New York
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For excellent recent surveys in asymmetric catalysis see (a) R. Noyori, Asymmetric Catalysis in Organic Synthesis, John Wiley and Sons Ltd., New York, 1994;
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(1994)
Asymmetric Catalysis in Organic Synthesis
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Noyori, R.1
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0003544583
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ed. I. Ojima, VCH Press, Berlin
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(b) Catalytic Asymmetric Synthesis, ed. I. Ojima, VCH Press, Berlin, 1993;
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(1993)
Catalytic Asymmetric Synthesis
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4
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33748620903
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Hydrogenation of compounds containing C=C, C=O and C=N bonds
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in the series, edited by S. Patai, The Chemistry of Double-Bonded Functional Groups Part 1, ch. 15
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Hydrogenation of compounds containing C=C, C=O and C=N bonds, by M. Wills, in the series Chemistry of the Functional Groups, edited by S. Patai, Supplement A3: The Chemistry of Double-Bonded Functional Groups Part 1, ch. 15, pp. 781-842.
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Chemistry of the Functional Groups
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Wills, M.1
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7
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0030800157
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(c) M. Palmer, T. Walsgrove and M. Wills, J. Org. Chem., 1997, 62, 5226 and references therein.
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Palmer, M.1
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8
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(a) B. Burns, J. R. Studley and M. Wills, Tetrahedron Lett., 1993, 34, 7105;
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Burns, B.1
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(b) B. Burns, N. P. King, J. R. Studley, H. Tye and M. Wills, Tetrahedron: Asymmetry, 1994, 5, 801;
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Burns, B.1
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0029983325
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(c) M. P. Gamble, J. R. Studley and M. Wills, Tetrahedron Lett., 1996, 37, 2853;
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(d) M. P. Gamble, J. R. Studley and M. Wills, Tetrahedron: Asymmetry, 1996, 7, 3071;
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(e) B. Burns, M. P. Gamble, A. R. C. Simm, J. R. Studley, N. W. Alcock and M. Wills, Tetrahedron: Asymmetry, 1997, 8, 73.
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Burns, B.1
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13
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0012365134
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D. Barr, W. Clegg, R. E. Mulvey and R. Snaith, J. Chem. Soc., Chem. Commun., 1984, 79;
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0001461597
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(c) S. E. Denmark, P. C. Miller and S. R. Wilson, J. Am. Chem. Soc., 1991, 113, 1468.
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0030027143
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(a) O. Chiodi, F. Fotiadu, M. Sylvestre and G. Buono, Tetrahedron Lett., 1996, 37, 39;
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Closely related reagents; (c) R. Hulst, H. Heres, N. C. M. W. Peper and R. M. Kellogg, Tetrahedron: Asymmetry, 1996, 7, 1373;
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33751157465
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(a) S. E. Denmark, D. M. Coe, N. E. Pratt, B. D. Griedel, J. Org. Chem., 1994, 59, 6161;
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0030586148
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0000779827
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0001505432
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28
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0001624426
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The oxazaphospholidine ring opening reaction of related compounds has been reported to proceed with retention of configuration at phosphorus, for example: J. M. Brown, J. V. Carey and M. J. H. Russell, Tetrahedron, 1990, 46, 4877.
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Brown, J.M.1
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0028352490
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(b) H. M. I. Osborn, A. A. Cantrill, J. B. Sweeney and B. Howson, Tetrahedron Lett., 1994, 35, 3159.
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31
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33748597922
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note
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The reaction between prolinol and diphenylphosphine chloride, in the presence of triethylamine and in dichloromethane solvent gave a large quantity of O-phosphinylated material. However the same reaction using diphenylprolinol gave mainly the N-phosphinylated product in 56% yield.
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32
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37049086631
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(a) J.-M. Brunel, O. Pardigon, B. Faure and G. Buono, J. Chem. Soc., Chem. Commun., 1992, 287;
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Brunel, J.-M.1
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0002433763
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(b) G. Buono, J.-M. Brunel, B. Faure and O. Pardigon, Phosphorus, Sulfur Silicon, 1993, 93, 43.
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Phosphorus, Sulfur Silicon
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Buono, G.1
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34
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0027425987
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J.-M. Brunel, M. Maffei and G. Buono, Tetrahedron: Asymmetry, 1993, 4, 2255.
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Tetrahedron: Asymmetry
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Brunel, J.-M.1
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35
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33748665499
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H. Tye, C. Eldred and M. Wills, J. Chem. Soc., Perkin Trans. 1, 1997, 457.
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J. Chem. Soc., Perkin Trans. 1
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Tye, H.1
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36
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0030272367
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(a) G. Brenchley, M. Fedouloff, E. Merifield and M. Wills, Tetrahedron: Asymmetry, 1996, 7, 2809;
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Brenchley, G.1
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37
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0001542550
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Corey, E.J.1
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0001698892
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Gawley, R.E.1
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0000190994
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0343427190
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