메뉴 건너뛰기




Volumn 576, Issue 1-2, 1999, Pages 195-202

Catalytic asymmetric reactions via π-allylpalladium complexes coordinated with chiral monophosphine ligands

Author keywords

Allylic substitution; Catalytic asymmetric reactions; Chiral monodendrate phosphine; Reduction; Allylpalladium

Indexed keywords

MOPS;

EID: 0001326728     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(98)01058-4     Document Type: Article
Times cited : (142)

References (43)
  • 1
    • 0001230815 scopus 로고
    • For reviews: (a) H. Brunner, Synthesis (1988) 645. (b) H. Brunner, Top. Stereochem. 18 (1988) 129. (c) R. Noyori, M. Kitamura, in: R. Scheffold (Ed.), Modern synthetic methods, vol. 5, Springer-Verlag, New York, 1989, p 115. (d) I. Ojima, N. Clos, C. Bastos, Tetrahedron 45 (1989) 6901. (e) I. Ojima, Catalytic asymmetric synthesis, VCH, New York, 1993. (f) R. Noyori, Asymmetric catalysis in organic synthesis, Wiley, New York, 1994.
    • (1988) Synthesis , pp. 645
    • Brunner, H.1
  • 2
    • 85050264385 scopus 로고
    • For reviews: (a) H. Brunner, Synthesis (1988) 645. (b) H. Brunner, Top. Stereochem. 18 (1988) 129. (c) R. Noyori, M. Kitamura, in: R. Scheffold (Ed.), Modern synthetic methods, vol. 5, Springer-Verlag, New York, 1989, p 115. (d) I. Ojima, N. Clos, C. Bastos, Tetrahedron 45 (1989) 6901. (e) I. Ojima, Catalytic asymmetric synthesis, VCH, New York, 1993. (f) R. Noyori, Asymmetric catalysis in organic synthesis, Wiley, New York, 1994.
    • (1988) Top. Stereochem. , vol.18 , pp. 129
    • Brunner, H.1
  • 3
    • 0001736112 scopus 로고
    • R. Scheffold (Ed.), Springer-Verlag, New York
    • For reviews: (a) H. Brunner, Synthesis (1988) 645. (b) H. Brunner, Top. Stereochem. 18 (1988) 129. (c) R. Noyori, M. Kitamura, in: R. Scheffold (Ed.), Modern synthetic methods, vol. 5, Springer-Verlag, New York, 1989, p 115. (d) I. Ojima, N. Clos, C. Bastos, Tetrahedron 45 (1989) 6901. (e) I. Ojima, Catalytic asymmetric synthesis, VCH, New York, 1993. (f) R. Noyori, Asymmetric catalysis in organic synthesis, Wiley, New York, 1994.
    • (1989) Modern Synthetic Methods , vol.5 , pp. 115
    • Noyori, R.1    Kitamura, M.2
  • 4
    • 0024368157 scopus 로고
    • For reviews: (a) H. Brunner, Synthesis (1988) 645. (b) H. Brunner, Top. Stereochem. 18 (1988) 129. (c) R. Noyori, M. Kitamura, in: R. Scheffold (Ed.), Modern synthetic methods, vol. 5, Springer-Verlag, New York, 1989, p 115. (d) I. Ojima, N. Clos, C. Bastos, Tetrahedron 45 (1989) 6901. (e) I. Ojima, Catalytic asymmetric synthesis, VCH, New York, 1993. (f) R. Noyori, Asymmetric catalysis in organic synthesis, Wiley, New York, 1994.
    • (1989) Tetrahedron , vol.45 , pp. 6901
    • Ojima, I.1    Clos, N.2    Bastos, C.3
  • 5
    • 0003544583 scopus 로고
    • VCH, New York
    • For reviews: (a) H. Brunner, Synthesis (1988) 645. (b) H. Brunner, Top. Stereochem. 18 (1988) 129. (c) R. Noyori, M. Kitamura, in: R. Scheffold (Ed.), Modern synthetic methods, vol. 5, Springer-Verlag, New York, 1989, p 115. (d) I. Ojima, N. Clos, C. Bastos, Tetrahedron 45 (1989) 6901. (e) I. Ojima, Catalytic asymmetric synthesis, VCH, New York, 1993. (f) R. Noyori, Asymmetric catalysis in organic synthesis, Wiley, New York, 1994.
    • (1993) Catalytic Asymmetric Synthesis
    • Ojima, I.1
  • 6
    • 0003400107 scopus 로고
    • Wiley, New York
    • For reviews: (a) H. Brunner, Synthesis (1988) 645. (b) H. Brunner, Top. Stereochem. 18 (1988) 129. (c) R. Noyori, M. Kitamura, in: R. Scheffold (Ed.), Modern synthetic methods, vol. 5, Springer-Verlag, New York, 1989, p 115. (d) I. Ojima, N. Clos, C. Bastos, Tetrahedron 45 (1989) 6901. (e) I. Ojima, Catalytic asymmetric synthesis, VCH, New York, 1993. (f) R. Noyori, Asymmetric catalysis in organic synthesis, Wiley, New York, 1994.
    • (1994) Asymmetric Catalysis in Organic Synthesis
    • Noyori, R.1
  • 9
    • 0000015844 scopus 로고    scopus 로고
    • and references cited therein
    • T. Hayashi, Acta Chem. Scand. 50 (1996) 259, and references cited therein.
    • (1996) Acta Chem. Scand. , vol.50 , pp. 259
    • Hayashi, T.1
  • 12
    • 6844254916 scopus 로고    scopus 로고
    • For reviews on catalytic asymmetric allylic substitutions: (a) B.M. Trost, D.L. Van Vranken, Chem. Rev. 96 (1996) 395. (b) G. Consiglio, R.M. Waymouth, Chem. Rev. 89 (1989) 257. (c) C.G. Frost, J. Howarth, J.M.J. Williams, Tetrahedron Asymmetry 3 (1992) 1089.
    • (1996) Chem. Rev. , vol.96 , pp. 395
    • Trost, B.M.1    Van Vranken, D.L.2
  • 13
    • 0024302311 scopus 로고
    • For reviews on catalytic asymmetric allylic substitutions: (a) B.M. Trost, D.L. Van Vranken, Chem. Rev. 96 (1996) 395. (b) G. Consiglio, R.M. Waymouth, Chem. Rev. 89 (1989) 257. (c) C.G. Frost, J. Howarth, J.M.J. Williams, Tetrahedron Asymmetry 3 (1992) 1089.
    • (1989) Chem. Rev. , vol.89 , pp. 257
    • Consiglio, G.1    Waymouth, R.M.2
  • 14
    • 0026722772 scopus 로고
    • For reviews on catalytic asymmetric allylic substitutions: (a) B.M. Trost, D.L. Van Vranken, Chem. Rev. 96 (1996) 395. (b) G. Consiglio, R.M. Waymouth, Chem. Rev. 89 (1989) 257. (c) C.G. Frost, J. Howarth, J.M.J. Williams, Tetrahedron Asymmetry 3 (1992) 1089.
    • (1992) Tetrahedron Asymmetry , vol.3 , pp. 1089
    • Frost, C.G.1    Howarth, J.2    Williams, J.M.J.3
  • 15
    • 0004809076 scopus 로고
    • (S)-(o-Methoxyphenyl)cyclohexylmethylphosphine ((S)-CAMP)
    • Examples of optically active monophosphine ligands: (a) (S)-(o-Methoxyphenyl)cyclohexylmethylphosphine ((S)-CAMP): W.S. Knowles, M.J. Sabacky, B.D. Vineyard, J. Chem. Soc. Chem. Commun. (1972) 10. (b) Neomentyldiphenylphosphine: J.D. Morrison, R.E. Burnett, A.M. Aguiar, C.J. Morrow, C. Phillips, J. Am. Chem. Soc. 93 (1971) 1301. (c) Ferrocenylmonophosphines: T. Hayashi, in: A. Togni, T. Hayashi (Eds.), Ferrocenes, VCH, Weinheim, 1995, p. 105.
    • (1972) J. Chem. Soc. Chem. Commun. , pp. 10
    • Knowles, W.S.1    Sabacky, M.J.2    Vineyard, B.D.3
  • 16
    • 33947291947 scopus 로고
    • Neomentyldiphenylphosphine
    • Examples of optically active monophosphine ligands: (a) (S)-(o- Methoxyphenyl)cyclohexylmethylphosphine ((S)-CAMP): W.S. Knowles, M.J. Sabacky, B.D. Vineyard, J. Chem. Soc. Chem. Commun. (1972) 10. (b) Neomentyldiphenylphosphine: J.D. Morrison, R.E. Burnett, A.M. Aguiar, C.J. Morrow, C. Phillips, J. Am. Chem. Soc. 93 (1971) 1301. (c) Ferrocenylmonophosphines: T. Hayashi, in: A. Togni, T. Hayashi (Eds.), Ferrocenes, VCH, Weinheim, 1995, p. 105.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 1301
    • Morrison, J.D.1    Burnett, R.E.2    Aguiar, A.M.3    Morrow, C.J.4    Phillips, C.5
  • 17
    • 0000135634 scopus 로고
    • Ferrocenylmonophosphines
    • A. Togni, T. Hayashi (Eds.), VCH, Weinheim
    • Examples of optically active monophosphine ligands: (a) (S)-(o- Methoxyphenyl)cyclohexylmethylphosphine ((S)-CAMP): W.S. Knowles, M.J. Sabacky, B.D. Vineyard, J. Chem. Soc. Chem. Commun. (1972) 10. (b) Neomentyldiphenylphosphine: J.D. Morrison, R.E. Burnett, A.M. Aguiar, C.J. Morrow, C. Phillips, J. Am. Chem. Soc. 93 (1971) 1301. (c) Ferrocenylmonophosphines: T. Hayashi, in: A. Togni, T. Hayashi (Eds.), Ferrocenes, VCH, Weinheim, 1995, p. 105.
    • (1995) Ferrocenes , pp. 105
    • Hayashi, T.1
  • 35
  • 38
    • 31544439675 scopus 로고    scopus 로고
    • For recent examples: (a) B.M. Trost, R.C. Bunt, Angew. Chem. Int. Ed. Engl. 35 (1996) 99. (b) G. Zhu, M. Terry, X. Zhang, Tetrahedron Lett. 37 (1996) 4475. (c) W. Zhang, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Lett. 37 (1996) 7995. (d) N. Nomura, Y.C. Mermet-Bouvier, T.V. RajanBabu, Synlett (1996) 745.
    • (1996) Angew. Chem. Int. Ed. Engl. , vol.35 , pp. 99
    • Trost, B.M.1    Bunt, R.C.2
  • 39
    • 0030600185 scopus 로고    scopus 로고
    • For recent examples: (a) B.M. Trost, R.C. Bunt, Angew. Chem. Int. Ed. Engl. 35 (1996) 99. (b) G. Zhu, M. Terry, X. Zhang, Tetrahedron Lett. 37 (1996) 4475. (c) W. Zhang, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Lett. 37 (1996) 7995. (d) N. Nomura, Y.C. Mermet-Bouvier, T.V. RajanBabu, Synlett (1996) 745.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 4475
    • Zhu, G.1    Terry, M.2    Zhang, X.3
  • 40
    • 0030605145 scopus 로고    scopus 로고
    • For recent examples: (a) B.M. Trost, R.C. Bunt, Angew. Chem. Int. Ed. Engl. 35 (1996) 99. (b) G. Zhu, M. Terry, X. Zhang, Tetrahedron Lett. 37 (1996) 4475. (c) W. Zhang, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Lett. 37 (1996) 7995. (d) N. Nomura, Y.C. Mermet-Bouvier, T.V. RajanBabu, Synlett (1996) 745.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 7995
    • Zhang, W.1    Kida, T.2    Nakatsuji, Y.3    Ikeda, I.4
  • 41
    • 0002560434 scopus 로고    scopus 로고
    • For recent examples: (a) B.M. Trost, R.C. Bunt, Angew. Chem. Int. Ed. Engl. 35 (1996) 99. (b) G. Zhu, M. Terry, X. Zhang, Tetrahedron Lett. 37 (1996) 4475. (c) W. Zhang, T. Kida, Y. Nakatsuji, I. Ikeda, Tetrahedron Lett. 37 (1996) 7995. (d) N. Nomura, Y.C. Mermet-Bouvier, T.V. RajanBabu, Synlett (1996) 745.
    • (1996) Synlett , pp. 745
    • Nomura, N.1    Mermet-Bouvier, Y.C.2    Rajanbabu, T.V.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.