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Volumn 59, Issue 48, 2003, Pages 9471-9515

Chiral P,N-ligands with pyridine-nitrogen and phosphorus donor atoms. Syntheses and applications in asymmetric catalysis

Author keywords

Asymmetric catalysis; Metal complexes; Pyridine phosphorus ligands

Indexed keywords

2 (2 PYRIDINYLCARBOXAMIDO) 2' (DIPHENYLPHOSPHANYL) 1,1' BINAPHTHYL; 2 (6 METHOXY 2 NAPHTHYL)PROPENOIC ACID; 2 (6 METHYL 2 PYRIDINYLCARBOXAMIDO) 2' (DIPHENYLPHOSPHANYL) 1,1 BINAPHTHYL; 2 [2 DIPHENYLPHOSPHINYL 1,7,7 TRIMETHYLBICYCLO[2.2.1]HEPT 2 YL]PYRIDINE; 3 ACRYLOYL 1,3 OXAZOLIDIN 2 ONE; ALKYL GROUP; BENZALDEHYDE; CYCLOPENTADIENE DERIVATIVE; DIETHYLZINC; KETONE DERIVATIVE; LIGAND; NAPHTHYL GROUP; NITROGEN; PHOSPHORUS; PYRIDINE DERIVATIVE; RHODIUM COMPLEX; UNCLASSIFIED DRUG; [1 DIPHENYLPHOSPHINYL 2 (2 METHYLETHYL) 5 METHYLCYCLOHEXYL]PYRIDINE;

EID: 0242269462     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2003.09.066     Document Type: Review
Times cited : (228)

References (130)
  • 19
    • 0030012272 scopus 로고    scopus 로고
    • (a) Ito K., Tabuchi S., Katsuki T. Synlett. 1992;575 (b) Ito K., Katsuki T. Tetrahedron Lett. 34:1993;575 (c) Ito K., Katsuki T. Chem. Lett. 1994;1857 (d) Ito K., Yoshitake M., Katsuki T. Tetrahedron. 52:1996;3905.
    • (1996) Tetrahedron , vol.52 , pp. 3905
    • Ito, K.1    Yoshitake, M.2    Katsuki, T.3
  • 22
    • 0002417273 scopus 로고
    • and references therein
    • Kröhnke F. Synthesis. 1976;1. and references therein.
    • (1976) Synthesis , pp. 1
    • Kröhnke, F.1
  • 27
    • 0028959981 scopus 로고
    • For a review on the cobalt-catalyzed synthesis of optically active pyridines, see:
    • For a review on the cobalt-catalyzed synthesis of optically active pyridines, see: Chelucci G. Tetrahedron: Asymmetry. 6:1995;811.
    • (1995) Tetrahedron: Asymmetry , vol.6 , pp. 811
    • Chelucci, G.1
  • 31
  • 35
    • 0030738342 scopus 로고    scopus 로고
    • (a) Brunel J.M., Constantieux T., Labande A., Lubatti F., Buono G. Tetrahedron Lett. 38:1997;5971 (b) Constantieux T., Brunel J.M., Labande A., Buono G. Synlett. 1998;49 (c) Brunel J.M., Del Campo B., Buono G. Tetrahedron Lett. 39:1998;9663 (d) Muchow G., Brunel J.M., Maffei M., Pardigon O., Buono G. Tetrahedron. 54:1998;10435 (e) Brunel J.M., Constantieux T., Buono G. J. Org. Chem. 64:1999;8940 (f) Brunel J.M., Tenaglia A., Buono G. Tetrahedron: Asymmetry. 11:2000;3585 (g) Delapierre G., Constantieux T., Brunel J.M., Buono G. Eur. J. Org. Chem. 2000;2507 (h) Delapierre G., Brunel J.M., Constantieux T., Buono G. Tetrahedron: Asymmetry. 12:2001;1345.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 5971
    • Brunel, J.M.1    Constantieux, T.2    Labande, A.3    Lubatti, F.4    Buono, G.5
  • 42
    • 0035844413 scopus 로고    scopus 로고
    • (a) Brunel J.M., Constantieux T., Labande A., Lubatti F., Buono G. Tetrahedron Lett. 38:1997;5971 (b) Constantieux T., Brunel J.M., Labande A., Buono G. Synlett. 1998;49 (c) Brunel J.M., Del Campo B., Buono G. Tetrahedron Lett. 39:1998;9663 (d) Muchow G., Brunel J.M., Maffei M., Pardigon O., Buono G. Tetrahedron. 54:1998;10435 (e) Brunel J.M., Constantieux T., Buono G. J. Org. Chem. 64:1999;8940 (f) Brunel J.M., Tenaglia A., Buono G. Tetrahedron: Asymmetry. 11:2000;3585 (g) Delapierre G., Constantieux T., Brunel J.M., Buono G. Eur. J. Org. Chem. 2000;2507 (h) Delapierre G., Brunel J.M., Constantieux T., Buono G. Tetrahedron: Asymmetry. 12:2001;1345.
    • (2001) Tetrahedron: Asymmetry , vol.12 , pp. 1345
    • Delapierre, G.1    Brunel, J.M.2    Constantieux, T.3    Buono, G.4
  • 72
    • 0033579623 scopus 로고    scopus 로고
    • This procedure has been reported in an independent related synthesis of racemic
    • This procedure has been reported in an independent related synthesis of racemic 157 : Quéguiner: Chapoulaud V.G., Audoux J., Plé N., Turck G., Quéguiner G. Tetrahedron Lett. 40:1999;9005.
    • (1999) Tetrahedron Lett. , vol.40 , pp. 9005
    • Chapoulaud, V.G.1    Audoux, J.2    Plé, N.3    Turck, G.4    Quéguiner, G.5
  • 88
    • 0001106268 scopus 로고    scopus 로고
    • (a) Ganter C., Blassat L., Ganter B. Organometallics. 16:1997;2862 (b) Ganter C., Blassat L., Ganter B. Chem. Ber. 130:1997;1771.
    • (1997) Chem. Ber. , vol.130 , pp. 1771
    • Ganter, C.1    Blassat, L.2    Ganter, B.3
  • 93
    • 0346156186 scopus 로고    scopus 로고
    • For reviews, see: (a) Helmchen G. J. Organomet. Chem. 576:1999;203 (b) Trost B.M., Van Vranken D.L. Chem. Rev. 96:1996;395 (c) Reiser O. Angew. Chem. 105:1993;576. Angew. Chem., Int. Ed. Engl. 1993, 32, 547 (d) Hayashi T. Ojima I. Catalytic Asymmetric Synthesis. 1993;VCH, Weinheim, (e) Frost C.G., Howarth J., Williams J.M.J. Tetrahedron: Asymmetry. 3:1992;1089.
    • (1999) J. Organomet. Chem. , vol.576 , pp. 203
    • Helmchen, G.1
  • 94
    • 6844254916 scopus 로고    scopus 로고
    • (b) Trost B.M., Van Vranken D.L. Chem. Rev. 96:1996;395 (c) Reiser O. Angew. Chem. 105:1993;576. Angew. Chem., Int. Ed. Engl. 1993, 32, 547 (d) Hayashi T. Ojima I. Catalytic Asymmetric Synthesis. 1993;VCH, Weinheim, (e) Frost C.G., Howarth J., Williams J.M.J. Tetrahedron: Asymmetry. 3:1992;1089.
    • (1996) Chem. Rev. , vol.96 , pp. 395
    • Trost, B.M.1    Van Vranken, D.L.2
  • 95
    • 0001064399 scopus 로고
    • For reviews, see: (a) Helmchen G. J. Organomet. Chem. 576:1999;203 (b) Trost B.M., Van Vranken D.L. Chem. Rev. 96:1996;395 (c) Reiser O. Angew. Chem. 105:1993;576. Angew. Chem., Int. Ed. Engl. 1993, 32, 547 (d) Hayashi T. Ojima I. Catalytic Asymmetric Synthesis. 1993;VCH, Weinheim, (e) Frost C.G., Howarth J., Williams J.M.J. Tetrahedron: Asymmetry. 3:1992;1089.
    • (1993) Angew. Chem. , vol.105 , pp. 576
    • Reiser, O.1
  • 96
    • 0003544583 scopus 로고
    • For reviews, see: (a) Helmchen G. J. Organomet. Chem. 576:1999;203 (b) Trost B.M., Van Vranken D.L. Chem. Rev. 96:1996;395 (c) Reiser O. Angew. Chem. 105:1993;576. Angew. Chem., Int. Ed. Engl. 1993, 32, 547 (d) Hayashi T. Ojima I. Catalytic Asymmetric Synthesis. 1993;VCH, Weinheim, (e) Frost C.G., Howarth J., Williams J.M.J. Tetrahedron: Asymmetry. 3:1992;1089.
    • (1993) Catalytic Asymmetric Synthesis
    • Hayashi, T.1
  • 97
    • 0026722772 scopus 로고
    • For reviews, see: (a). Angew. Chem., Int. Ed. Engl. 1993, 32, 547. I. Ojima. VCH, Weinheim
    • For reviews, see: (a) Helmchen G. J. Organomet. Chem. 576:1999;203 (b) Trost B.M., Van Vranken D.L. Chem. Rev. 96:1996;395 (c) Reiser O. Angew. Chem. 105:1993;576. Angew. Chem., Int. Ed. Engl. 1993, 32, 547 (d) Hayashi T. Ojima I. Catalytic Asymmetric Synthesis. 1993;VCH, Weinheim, (e) Frost C.G., Howarth J., Williams J.M.J. Tetrahedron: Asymmetry. 3:1992;1089.
    • (1992) Tetrahedron: Asymmetry , vol.3 , pp. 1089
    • Frost, C.G.1    Howarth, J.2    Williams, J.M.J.3
  • 101
    • 0001085039 scopus 로고
    • (a) Beletskaya A., Pelter A. Tetrahedron. 53:1997;4957 (b) Burgess K., Ohlmeyer M.J. Chem. Rev. 91:1991;1179.
    • (1991) Chem. Rev. , vol.91 , pp. 1179
    • Burgess, K.1    Ohlmeyer, M.J.2
  • 112
    • 0032536551 scopus 로고    scopus 로고
    • Pergamon, Oxford
    • (a) Perlmutter P. Conjugated Addition Reactions in Organic Synthesis. 1992;Pergamon, Oxford, (b) Lipshutz B.H., Sengupta S. Org. React. 41:1992;135 (c) Rossiter B.E., Swingle N.M. Chem. Rev. 92:1992;771 (d) Krause N. Angew. Chem. Int. Ed. Engl. 37:1998;283.
    • (1998) Angew. Chem. Int. Ed. Engl. , vol.37 , pp. 283
    • Krause, N.1
  • 115
    • 0000701744 scopus 로고    scopus 로고
    • Hydrogrenation of Carbon-Carbon Double Bonds
    • E.N. Jacobsen, A. Pfaltz, & H. Yamamoto. Berlin: Springer. Chapter 5
    • Brown J.M. Hydrogrenation of Carbon-Carbon Double Bonds. Jacobsen E.N., Pfaltz A., Yamamoto H. Comprehensive Asymmetric Catalysis. Vol. 1:1999;121-198 Springer, Berlin. Chapter 5.
    • (1999) Comprehensive Asymmetric Catalysis , vol.1 , pp. 121-198
    • Brown, J.M.1
  • 118
    • 0001831183 scopus 로고    scopus 로고
    • Transfer Hydrogenation
    • (a) Gladiali S., Mestroni G. Transfer Hydrogenation. Jacobsen E.N., Pfaltz A., Yamamoto H. Comprehensive Asymmetric Catalysis. Vol. 2:1999;97-119 Springer, Berlin. Chapter 21
    • (1999) Comprehensive Asymmetric Catalysis , vol.2 , pp. 97-119
    • Gladiali, S.1    Mestroni, G.2
  • 119
    • 4243378570 scopus 로고
    • E.N. Jacobsen, A. Pfaltz, & H. Yamamoto. Berlin: Springer. Chapter 21
    • (a) Gladiali S., Mestroni G. Transfer Hydrogenation. Jacobsen E.N., Pfaltz A., Yamamoto H. Comprehensive Asymmetric Catalysis. Vol. 2:1999;97-119 Springer, Berlin. Chapter 21 (b) Zassinovich G., Mestroni G., Gladiali S. Chem. Rev. 92:1992;1051.
    • (1992) Chem. Rev. , vol.92 , pp. 1051
    • Zassinovich, G.1    Mestroni, G.2    Gladiali, S.3
  • 120
    • 0000421290 scopus 로고    scopus 로고
    • Hydrosilylations of Carbonyland Imino Groups
    • (a) Nishiyama H. Hydrosilylations of Carbonyland Imino Groups. Jacobsen E.N., Pfaltz A., Yamamoto H. Comprehensive Asymmetric Catalysis. Vol. 1:1999;267-288 Springer, Berlin. Chapter 6
    • (1999) Comprehensive Asymmetric Catalysis , vol.1 , pp. 267-288
    • Nishiyama, H.1
  • 121
    • 0002528937 scopus 로고
    • E.N. Jacobsen, A. Pfaltz, & H. Yamamoto. Berlin: Springer. Chapter 6. I. Ojima. New York: VCH
    • (a) Nishiyama H. Hydrosilylations of Carbonyland Imino Groups. Jacobsen E.N., Pfaltz A., Yamamoto H. Comprehensive Asymmetric Catalysis. Vol. 1:1999;267-288 Springer, Berlin. Chapter 6 (b) Brunner H., Nishiyama H., Itoh K. Ojima I. Catalytic Asymmetric Synthesis. 1993;303 VCH, New York.
    • (1993) Catalytic Asymmetric Synthesis , pp. 303
    • Brunner, H.1    Nishiyama, H.2    Itoh, K.3
  • 123
    • 4244033876 scopus 로고
    • For a review, see: (a)
    • For a review, see: (a) Diaz I.C. J. Braz. Chem. Soc. 8:1997;289 (b) Kagan H.B., Riant O. Chem. Rev. 92:1992;1007.
    • (1992) Chem. Rev. , vol.92 , pp. 1007
    • Kagan, H.B.1    Riant, O.2
  • 126
    • 0004225917 scopus 로고    scopus 로고
    • Cross-Coupling Reactions
    • E.N. Jacobsen, A. Pfaltz, & H. Yamamoto. Berlin: Springer. Chapter 25
    • Hayashi T. Cross-Coupling Reactions. Jacobsen E.N., Pfaltz A., Yamamoto H. Comprehensive Asymmetric Catalysis. Vol. 2:1999;889-907 Springer, Berlin. Chapter 25.
    • (1999) Comprehensive Asymmetric Catalysis , vol.2 , pp. 889-907
    • Hayashi, T.1
  • 129
    • 0032500082 scopus 로고    scopus 로고
    • For recent reviews on cyclopropanation, see: (a) Doyle M.P., McKervey M.A., Ye T. Modern Catalytic Methods for Organic Synthesis with Diazo Compounds. 1998;Wiley, New York, (b) Doyle M.P., Protonova M.N. Tetrahedron. 54:1998;7919 (c) Singh V.K., DattaGupta A., Sekar G. Synthesis. 1997;137.
    • (1998) Tetrahedron , vol.54 , pp. 7919
    • Doyle, M.P.1    Protonova, M.N.2
  • 130
    • 0007992871 scopus 로고    scopus 로고
    • For recent reviews on cyclopropanation, see: (a). Wiley, New York Giorgio Chelucci was born in Cagliari (Sardegna
    • For recent reviews on cyclopropanation, see: (a) Doyle M.P., McKervey M.A., Ye T. Modern Catalytic Methods for Organic Synthesis with Diazo Compounds. 1998;Wiley, New York, (b) Doyle M.P., Protonova M.N. Tetrahedron. 54:1998;7919 (c) Singh V.K., DattaGupta A., Sekar G. Synthesis. 1997;137.
    • (1997) Synthesis , pp. 137
    • Singh, V.K.1    DattaGupta, A.2    Sekar, G.3


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