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Volumn 11, Issue 16, 2000, Pages 3427-3438

Chiral 2,2′-bipyridines, 5,6-dihydro-1,10-phenanthrolines and 1,10-phenanthrolines as ligands for enantioselective palladium catalyzed allylic substitution

Author keywords

[No Author keywords available]

Indexed keywords

BIPYRIDINE DERIVATIVE; LIGAND; PHENANTHROLINE DERIVATIVE; QUINOLINE DERIVATIVE;

EID: 0034714142     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(00)00296-2     Document Type: Article
Times cited : (40)

References (19)
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    • (1999) J. Organomet. Chem. , vol.576 , pp. 203
    • Helmchen, G.1
  • 4
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    • Helmchen, G. J. Organomet. Chem. 1999, 576, 203. Trost, B. M.; Van Vranken, D. L. Chem. Rev. 1996, 96, 395. Reiser, O. Angew. Chem. 1993, 105, 576; Angew. Chem., Int. Ed. Engl. 1993, 32, 547. Hayashi, T. In Catalytic Asymmetric Synthesis; Ojima, Ed.; VCH: Weinheim, 1993. Frost, C. G.; Howarth, J.; Williams, J. M. J. Tetrahedron: Asymmetry 1992, 3, 1089. 3.
    • (1996) Chem. Rev. , vol.96 , pp. 395
    • Trost, B.M.1    Van Vranken, D.L.2
  • 5
    • 0001064399 scopus 로고
    • Helmchen, G. J. Organomet. Chem. 1999, 576, 203. Trost, B. M.; Van Vranken, D. L. Chem. Rev. 1996, 96, 395. Reiser, O. Angew. Chem. 1993, 105, 576; Angew. Chem., Int. Ed. Engl. 1993, 32, 547. Hayashi, T. In Catalytic Asymmetric Synthesis; Ojima, Ed.; VCH: Weinheim, 1993. Frost, C. G.; Howarth, J.; Williams, J. M. J. Tetrahedron: Asymmetry 1992, 3, 1089. 3.
    • (1993) Angew. Chem. , vol.105 , pp. 576
    • Reiser, O.1
  • 6
    • 33748245787 scopus 로고
    • Helmchen, G. J. Organomet. Chem. 1999, 576, 203. Trost, B. M.; Van Vranken, D. L. Chem. Rev. 1996, 96, 395. Reiser, O. Angew. Chem. 1993, 105, 576; Angew. Chem., Int. Ed. Engl. 1993, 32, 547. Hayashi, T. In Catalytic Asymmetric Synthesis; Ojima, Ed.; VCH: Weinheim, 1993. Frost, C. G.; Howarth, J.; Williams, J. M. J. Tetrahedron: Asymmetry 1992, 3, 1089. 3.
    • (1993) Angew. Chem., Int. Ed. Engl. , vol.32 , pp. 547
  • 7
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    • Ojima, Ed.; VCH: Weinheim
    • Helmchen, G. J. Organomet. Chem. 1999, 576, 203. Trost, B. M.; Van Vranken, D. L. Chem. Rev. 1996, 96, 395. Reiser, O. Angew. Chem. 1993, 105, 576; Angew. Chem., Int. Ed. Engl. 1993, 32, 547. Hayashi, T. In Catalytic Asymmetric Synthesis; Ojima, Ed.; VCH: Weinheim, 1993. Frost, C. G.; Howarth, J.; Williams, J. M. J. Tetrahedron: Asymmetry 1992, 3, 1089. 3.
    • (1993) Catalytic Asymmetric Synthesis
    • Hayashi, T.1
  • 8
    • 84991428681 scopus 로고
    • Helmchen, G. J. Organomet. Chem. 1999, 576, 203. Trost, B. M.; Van Vranken, D. L. Chem. Rev. 1996, 96, 395. Reiser, O. Angew. Chem. 1993, 105, 576; Angew. Chem., Int. Ed. Engl. 1993, 32, 547. Hayashi, T. In Catalytic Asymmetric Synthesis; Ojima, Ed.; VCH: Weinheim, 1993. Frost, C. G.; Howarth, J.; Williams, J. M. J. Tetrahedron: Asymmetry 1992, 3, 1089. 3.
    • (1992) J. Tetrahedron: Asymmetry , vol.3 , pp. 10893
    • Frost, C.G.1    Howarth, J.2    Williams, J.M.3
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    • Chelucci, G.; Culeddu, N.; Saba, A.; Valenti, R. Tetrahedron: Asymmetry 1999, 10, 3537. Koning, B., Meetsma, A., Kellogg, R. M. J. Org. Chem 1998, 63, 5533.
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  • 13
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    • 3-allyl complexes with phenanthroline ligands has been reported only in the case of allylic systems with small substituents. With bulky substituents, such as phenyl, the syn, syn geometry is greatly favoured: and references therein
    • 3-allyl complexes with phenanthroline ligands has been reported only in the case of allylic systems with small substituents. With bulky substituents, such as phenyl, the syn, syn geometry is greatly favoured: Poña-Cabrera, E.; Norby, P. O.; Sjógren, M.; Vitagliano, A.; De Felice, V.; Oslob, I.; Ishii, S.; O’Neill, D.; Åkermark, B.; Helquist, P. J. Am. Chem. Soc. 1996, 118, 4299 and references therein.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 4299
    • Poña-Cabrera, E.1    Norby, P.O.2    Sjógren, M.3    Vitagliano, A.4    De Felice, V.5    Oslob, I.6    Ishii, S.7    O’Neill, D.8    Åkermark, B.9    Helquist, P.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.