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Volumn 35, Issue 7, 1996, Pages 2157-2161

Synthesis and Conformation of Chiral Eight-Membered 12H-Dibenzo[d,g][1,3,2]dioxaphosphocins

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EID: 0000119663     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic951130p     Document Type: Article
Times cited : (15)

References (113)
  • 1
    • 0003905731 scopus 로고
    • Academic Press: New York
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1983) Asymmetric Synthesis , vol.5
    • Morrison, J.D.1
  • 2
    • 0003601187 scopus 로고
    • Plenum: New York
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1983) Homogeneous Catalysis with Metal Phosphine Complexes
    • Pignolet, L.H.1
  • 3
    • 0003694525 scopus 로고
    • Butterworths: London
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1986) Handbook of Coordination Catalyst in Organic Chemistry
    • Chaloner, P.A.1
  • 4
    • 0001230815 scopus 로고
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1988) Synthesis , pp. 645
    • Brunner, H.1
  • 5
    • 85050264385 scopus 로고
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1988) Top. Stereochem. , vol.18 , pp. 129
    • Brunner, H.1
  • 6
    • 38349178524 scopus 로고
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1989) Mod. Synth. Methods , vol.5 , pp. 155
    • Noyori, R.1    Kitamura, M.2
  • 7
    • 0024368157 scopus 로고
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1989) Tetrahedron , vol.45 , pp. 6901
    • Ojima, I.1    Clos, N.2    Bastos, C.3
  • 8
    • 0001247165 scopus 로고
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1990) Acc. Chem. Res. , vol.23 , pp. 345
    • Noyori, R.1    Takaya, H.2
  • 9
    • 0042250061 scopus 로고
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1992) Chem. Rev. , vol.92 , pp. 857
    • Sasaya, M.1    Ito, Y.2
  • 10
    • 0742318457 scopus 로고
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1992) Chem. Rev. , vol.92 , pp. 935
    • Blaser, H.-U.1
  • 11
    • 2742536303 scopus 로고
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1992) Engl. Transl. , vol.28 , pp. 1913
    • Dunina, V.V.1    Beletskaya, I.P.2
  • 12
    • 0003544583 scopus 로고
    • VCH: Weinheim, Germany
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1993) Catalytic Asymmetric Synthesis
    • Ojima, I.1
  • 13
    • 0003400107 scopus 로고
    • Wiley Interscience: New York
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1994) Asymmetric Catalysis in Organic Synthesis
    • Noyori, R.1
  • 14
    • 0003942864 scopus 로고
    • Wiley-Interscience: New York.
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1994) Stereochemistry of Organic Compounds
    • Eliel, E.L.1    Wilen, S.H.2
  • 15
    • 0003643894 scopus 로고
    • Wiley: New York
    • For a reviews, see: (a) Morrison, J. D. Asymmetric Synthesis; Academic Press: New York, 1983; Vol. 5. (b) Pignolet, L H. Homogeneous Catalysis with Metal Phosphine Complexes; Plenum: New York, 1983. Chaloner, P. A. Handbook of Coordination Catalyst in Organic Chemistry; Butterworths: London, 1986. Brunner, H. Synthesis 1988, 645. (e) Brunner, H. Top. Stereochem. 1988, 18, 129. (f) Noyori, R., Kitamura, M. Mod. Synth. Methods 1989, 5, 155. (g) Ojima, I.; Clos, N.; Bastos, C. Tetrahedron 1989, 45, 6901. (h) Noyori, R.; Takaya, H. Acc. Chem. Res. 1990, 23, 345. Sasaya, M ; Ito, Y. Chem. Rev. 1992, 92, 857. (j) Blaser, H.-U. Chem. Rev. 1992, 92, 935. (k) Dunina, V. V.; Beletskaya, I. P. (Engl. Transl.) 1992, 28, 1913. Ojima, I. Catalytic Asymmetric Synthesis; VCH: Weinheim, Germany, 1993. Noyori, R. Asymmetric Catalysis in Organic Synthesis; Wiley Interscience: New York, 1994. (n) For a review of stereochemical principles and current nomenclature, see: Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds; Wiley-Interscience: New York. 1994. (o) Seyden - Penne, J. Chiral Auxiliaries and Ligands in Asymmetric Synthesis; Wiley: New York, 1995.
    • (1995) Chiral Auxiliaries and Ligands in Asymmetric Synthesis
    • Seyden Penne, J.1
  • 16
    • 2742519751 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1966) J. Gen. Chem. USSR (Engl. Transl.) , vol.36 , pp. 1137
    • Nifant'ev, E.E.1    Tuseev, A.P.2    Tarasov, V.V.3
  • 17
    • 0342916395 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1966) Zh. Obshch. Khim. , vol.36 , pp. 1124
  • 18
    • 2042442223 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1978) J Organomet. Chem. , vol.750
    • Descotes, G.1    Lafont, D.2    Sinou, D.3
  • 19
    • 0002654408 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1979) J. Organomet. Chem. , vol.169 , pp. 87
    • Lafont, D.1    Sinou, D.2    Descotes, G.3
  • 20
    • 24444446968 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1980) Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) , pp. 1324
    • Dzhemilev, U.M.1    Fakhretdinov, R.N.2    Telin, A.G.3    Tolstikov, G.A.4
  • 21
    • 24444476629 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1980) Izv. Akad. Nauk SSSR, Ser. Khim. , pp. 944
  • 22
    • 34250246587 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1980) Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) , pp. 1943
    • Dzhemilev, U.M.1    Fakhretdinov, R.N.2    Telin, A.G.3    Tolstikov, G.A.4    Panasenko, A.A.5    Vasil'eva, E.V.6
  • 23
    • 24444448930 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1980) Izv. Akad. Nauk SSSR, Ser. Khim. , pp. 2771
  • 24
    • 0038516024 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1983) Nouv. J Chim. , vol.7 , pp. 593
    • Petit, M.1    Mortreux, A.2    Petit, F.3    Buono, G.4    Peiffer, G.5
  • 25
    • 24444450291 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1984) Carbohydr. Res. , vol.131
    • Yamashita, M.1    Kobayashi, M.2    Sugiura, M.3    Oshikawa, T.4    Inokawa, S.5    Yamamoto, H.6
  • 26
    • 0242461567 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1985) Chem. Pharm. Bull. , vol.33 , pp. 5284
    • Saito, S.1    Nakamura, Y.2    Monta, Y.3
  • 27
    • 2742521866 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1985) J. Organomet. Chem. , vol.288
    • Massonneau, V.1    Le Maux, P.2    Simonneaux, G.3
  • 28
    • 0142214972 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1985) J Organomet. Chem. , vol.284 , pp. 101
    • Le Maux, P.1    Massonneau, V.2    Simonneaux, G.3
  • 29
    • 0039029992 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1988) Bull. Chem. Soc Jpn. , vol.61 , pp. 2365
    • Iida, A.1    Yamashita, M.2
  • 30
    • 0042048354 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1989) J. Organomet. Chem. , vol.362 , pp. 411
    • Felföldi, K.1    Kapocsi, I.2    Bartók, M.3
  • 31
    • 0004495490 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1989) Bull. Chem Soc. Jpn. , vol.62 , pp. 942
    • Yamashita, M.1    Naoi, M.2    Imoto, H.3    Oshikawa, T.4
  • 32
    • 2742544029 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1989) Sulfur Lett. , vol.9 , pp. 39
    • Pastor, S.D.1
  • 33
    • 84887148034 scopus 로고
    • For carbohydrate-derived phosphorus ligands, see: (a) Nifant'ev, E. E.; Tuseev, A. P.; Tarasov, V V. J. Gen. Chem. USSR (Engl. Transl.) 1966, 36, 1137; Zh. Obshch. Khim. 1966, 36, 1124. (b) Descotes, G.; Lafont, D ; Sinou, D. J Organomet. Chem. 1978, 750, C14. Lafont, D.; Sinou, D.; Descotes, G. J. Organomet. Chem. 1979, 169, 87. Dzhemilev, U. M ; Fakhretdinov, R. N., Telin, A. G ; Tolstikov, G. A. Proc. Natl. Acad. Sci. USSR. Chem. Sec. (Engl. Transl.) 1980, 1324; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 944. (e) Dzhemilev, U. M ; Fakhretdinov, R. N.; Telin, A. G.; Tolstikov, G. A., Panasenko, A. A.; Vasil'eva, E. V. Proc. Natl. Acad. Sci. USSR. Chem. Sect. (Engl. Transl.) 1980, 1943; Izv. Akad. Nauk SSSR, Ser. Khim. 1980, 2771. (f) Petit, M.; Mortreux, A.; Petit, F.; Buono, G., Peiffer, G. Nouv. J Chim. 1983, 7, 593. (g) Yamashita, M.; Kobayashi, M.; Sugiura, M.; Oshikawa, T.; Inokawa, S., Yamamoto, H. Carbohydr. Res. 1984, 131, C6. (h) Saito, S.; Nakamura, Y.; Monta, Y Chem. Pharm. Bull. 1985, 33, 5284. Massonneau, V.; Le Maux, P.; Simonneaux, G. J. Organomet. Chem.1985, 288, C59. (j) Le Maux, P.; Massonneau, V.; Simonneaux, G. J Organomet. Chem. 1985, 284, 101. (k) Iida A.; Yamashita, M. Bull. Chem. Soc Jpn. 1988, 61, 2365. Felföldi, K.; Kapocsi, I.; Bartók, M. J. Organomet. Chem. 1989, 362, 411. Yamashita, M.; Naoi, M.; Imoto, H.; Oshikawa, T. Bull. Chem Soc. Jpn. 1989, 62, 942. (n) Pastor, S. D. Sulfur Lett. 1989, 9, 39. (o) Babiarz, J. E., Pastor, S. D. Phosphorus, Sulfur, Silicon Relat. Elem. 1994, 91, 263.
    • (1994) Phosphorus, Sulfur, Silicon Relat. Elem. , vol.91 , pp. 263
    • Babiarz, J.E.1    Pastor, S.D.2
  • 42
    • 0000918242 scopus 로고
    • U S Patent 5,360,938, 1994
    • See also: (b) Babin, J. E.; Whiteker, G. T. U S Patent 5,360,938, 1994; Chem. Abstr. 1995, 122, 186-609.
    • (1995) Chem. Abstr. , vol.122 , pp. 186-609
    • Babin, J.E.1    Whiteker, G.T.2
  • 45
    • 0002998461 scopus 로고
    • See also: Jongsma, T.; Fossen, M ; Challa, G.; van Leeuwen, P. W. N. M. J. Mol. Catal. 1993, 83, 17. van Rooy, A.; Orij, E. N.; Kamer, P. C. J.; van Leeuwen, P. W. N. M. Organometallics 1995, 14, 34. (e) Buisman, G. J. H.; Martin, M. E.; Vos, E. J.; Klootwijk, A.; Kamer, P. C. J.; van Leeuwen, P. W. N M. Tetrahedron: Asymmetry 1995, 6, 719. (f) van Rooy, A.; Kamer, P. C. J., van Leeuwen, P. W. N. M.; Veldman, N.; Spek, A. L. J. Organomet. Chem. 1995, 494, C15.
    • (1993) J. Mol. Catal. , vol.83 , pp. 17
    • Jongsma, T.1    Fossen, M.2    Challa, G.3    Van Leeuwen, P.W.N.M.4
  • 46
    • 0003123886 scopus 로고
    • See also: Jongsma, T.; Fossen, M ; Challa, G.; van Leeuwen, P. W. N. M. J. Mol. Catal. 1993, 83, 17. van Rooy, A.; Orij, E. N.; Kamer, P. C. J.; van Leeuwen, P. W. N. M. Organometallics 1995, 14, 34. (e) Buisman, G. J. H.; Martin, M. E.; Vos, E. J.; Klootwijk, A.; Kamer, P. C. J.; van Leeuwen, P. W. N M. Tetrahedron: Asymmetry 1995, 6, 719. (f) van Rooy, A.; Kamer, P. C. J., van Leeuwen, P. W. N. M.; Veldman, N.; Spek, A. L. J. Organomet. Chem. 1995, 494, C15.
    • (1995) Organometallics , vol.14 , pp. 34
    • Van Rooy, A.1    Orij, E.N.2    Kamer, P.C.J.3    Van Leeuwen, P.W.N.M.4
  • 47
    • 0028912270 scopus 로고
    • See also: Jongsma, T.; Fossen, M ; Challa, G.; van Leeuwen, P. W. N. M. J. Mol. Catal. 1993, 83, 17. van Rooy, A.; Orij, E. N.; Kamer, P. C. J.; van Leeuwen, P. W. N. M. Organometallics 1995, 14, 34. (e) Buisman, G. J. H.; Martin, M. E.; Vos, E. J.; Klootwijk, A.; Kamer, P. C. J.; van Leeuwen, P. W. N M. Tetrahedron: Asymmetry 1995, 6, 719. (f) van Rooy, A.; Kamer, P. C. J., van Leeuwen, P. W. N. M.; Veldman, N.; Spek, A. L. J. Organomet. Chem. 1995, 494, C15.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 719
    • Buisman, G.J.H.1    Martin, M.E.2    Vos, E.J.3    Klootwijk, A.4    Kamer, P.C.J.5    Van Leeuwen, P.W.N.M.6
  • 48
    • 0002319956 scopus 로고
    • See also: Jongsma, T.; Fossen, M ; Challa, G.; van Leeuwen, P. W. N. M. J. Mol. Catal. 1993, 83, 17. van Rooy, A.; Orij, E. N.; Kamer, P. C. J.; van Leeuwen, P. W. N. M. Organometallics 1995, 14, 34. (e) Buisman, G. J. H.; Martin, M. E.; Vos, E. J.; Klootwijk, A.; Kamer, P. C. J.; van Leeuwen, P. W. N M. Tetrahedron: Asymmetry 1995, 6, 719. (f) van Rooy, A.; Kamer, P. C. J., van Leeuwen, P. W. N. M.; Veldman, N.; Spek, A. L. J. Organomet. Chem. 1995, 494, C15.
    • (1995) J. Organomet. Chem. , vol.494
    • Van Rooy, A.1    Kamer, P.C.J.2    Van Leeuwen, P.W.N.M.3    Veldman, N.4    Spek, A.L.5
  • 49
    • 85005607967 scopus 로고
    • For the relationship between the ratio of normal to iso olefin hydroformylation as a function of ligand bite angle, see: (a) Casey, C. P.; Whiteker, G. T. Isr. J. Chem. 1990, 3, 299. (b) Casey, C. P.; Whiteker, G T. J. Org. Chem. 1990, 55, 1394. Casey, C. P.; Whiteker, G. T.; Campana, C. F., Powell, D. R.; Inorg. Chem. 1990, 29, 3376. Casey, C. P.; Whiteker, G. T., Melville, M. G., Petrovich, L. M.; Gavney, J. A., Jr., Powell, D. R. J. Am. Chem. Soc. 1992, 114, 5535.
    • (1990) Isr. J. Chem. , vol.3 , pp. 299
    • Casey, C.P.1    Whiteker, G.T.2
  • 50
    • 0025308555 scopus 로고
    • For the relationship between the ratio of normal to iso olefin hydroformylation as a function of ligand bite angle, see: (a) Casey, C. P.; Whiteker, G. T. Isr. J. Chem. 1990, 3, 299. (b) Casey, C. P.; Whiteker, G T. J. Org. Chem. 1990, 55, 1394. Casey, C. P.; Whiteker, G. T.; Campana, C. F., Powell, D. R.; Inorg. Chem. 1990, 29, 3376. Casey, C. P.; Whiteker, G. T., Melville, M. G., Petrovich, L. M.; Gavney, J. A., Jr., Powell, D. R. J. Am. Chem. Soc. 1992, 114, 5535.
    • (1990) J. Org. Chem. , vol.55 , pp. 1394
    • Casey, C.P.1    Whiteker, G.T.2
  • 51
    • 0000714569 scopus 로고
    • For the relationship between the ratio of normal to iso olefin hydroformylation as a function of ligand bite angle, see: (a) Casey, C. P.; Whiteker, G. T. Isr. J. Chem. 1990, 3, 299. (b) Casey, C. P.; Whiteker, G T. J. Org. Chem. 1990, 55, 1394. Casey, C. P.; Whiteker, G. T.; Campana, C. F., Powell, D. R.; Inorg. Chem. 1990, 29, 3376. Casey, C. P.; Whiteker, G. T., Melville, M. G., Petrovich, L. M.; Gavney, J. A., Jr., Powell, D. R. J. Am. Chem. Soc. 1992, 114, 5535.
    • (1990) Inorg. Chem. , vol.29 , pp. 3376
    • Casey, C.P.1    Whiteker, G.T.2    Campana, C.F.3    Powell, D.R.4
  • 52
    • 11944256836 scopus 로고
    • For the relationship between the ratio of normal to iso olefin hydroformylation as a function of ligand bite angle, see: (a) Casey, C. P.; Whiteker, G. T. Isr. J. Chem. 1990, 3, 299. (b) Casey, C. P.; Whiteker, G T. J. Org. Chem. 1990, 55, 1394. Casey, C. P.; Whiteker, G. T.; Campana, C. F., Powell, D. R.; Inorg. Chem. 1990, 29, 3376. Casey, C. P.; Whiteker, G. T., Melville, M. G., Petrovich, L. M.; Gavney, J. A., Jr., Powell, D. R. J. Am. Chem. Soc. 1992, 114, 5535.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 5535
    • Casey, C.P.1    Whiteker, G.T.2    Melville, M.G.3    Petrovich, L.M.4    Gavney Jr., J.A.5    Powell, D.R.6
  • 57
    • 0004069268 scopus 로고
    • ACS Monograph 176; American Chemical Society: Washington, DC
    • For reviews, see: (a) Luckenbach, R. Dynamic Stereochemistry of Pentacoordinated Phosphorus and Related Elements; G. Thieme: Stuttgart, Germany, 1973. (b) Holmes, R. R. Pentacoordinated Phosphorus: Reaction Mechansisms, Vol. 1; ACS Monograph 176; American Chemical Society: Washington, DC, 1980.
    • (1980) Pentacoordinated Phosphorus: Reaction Mechansisms , vol.1
    • Holmes, R.R.1
  • 76
    • 85086527069 scopus 로고    scopus 로고
    • 31P chemical shift for 4 reported in ref 29 is incorrect
    • 31P chemical shift for 4 reported in ref 29 is incorrect.
  • 94
    • 85086527144 scopus 로고    scopus 로고
    • 3
    • 3.
  • 95
    • 2742596626 scopus 로고    scopus 로고
    • Minor peaking observed in the baseline corresponding to unidentified complexes at 110 °C. Upon cooling, the original spectrum is observed
    • Minor peaking observed in the baseline corresponding to unidentified complexes at 110 °C. Upon cooling, the original spectrum is observed.
  • 96
    • 0003670183 scopus 로고
    • Verkade, J. G., Quin, L. D., Eds., VCH: Weinheim, Germany, and references therein
    • PP coupling constants in dimeric Pt complexes, see: Pregosm, P. S. In Phosphorus-31 NMR Spectroscopy in Stere ochemical Analysis; Verkade, J. G., Quin, L. D., Eds., VCH: Weinheim, Germany, 1987; pp 465-530 and references therein.
    • (1987) Phosphorus-31 NMR Spectroscopy in Stere Ochemical Analysis , pp. 465-530
    • Pregosm, P.S.1


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