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Volumn 1, Issue 20, 2003, Pages 3586-3591

Synthesis of planar chiral ferrocenyl 1,3-diamines and 1,3-amino ethers

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; COPPER OXIDES; DIMERS; ORGANIC ACIDS; SINGLE CRYSTALS; SYNTHESIS (CHEMICAL); X RAY DIFFRACTION ANALYSIS;

EID: 0142227197     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b307014j     Document Type: Article
Times cited : (22)

References (46)
  • 1
    • 2142858973 scopus 로고    scopus 로고
    • ed. A. Togni and R. L. Halterman, Wiley-VCH, Weinheim, Germany, ch. 10
    • A. Togni, in Metallocenes, ed. A. Togni and R. L. Halterman, Wiley-VCH, Weinheim, Germany, 1998, vol. 2, ch. 10.
    • (1998) Metallocenes , vol.2
    • Togni, A.1
  • 2
    • 0142204122 scopus 로고    scopus 로고
    • ed. E. N. Jacobsen, A. Pfaltz and H. Yamamoto, Springer-Verlag, Berlin, Germany, ch. 41.1
    • H.-U. Blaserand F. Spindler, in Comprehensive Asymmetric Catalysis I-III, ed. E. N. Jacobsen, A. Pfaltz and H. Yamamoto, Springer-Verlag, Berlin, Germany, 1999, ch. 41.1.
    • (1999) Comprehensive Asymmetric Catalysis I-III
    • Blaserand, H.-U.1    Spindler, F.2
  • 7
    • 0037459506 scopus 로고    scopus 로고
    • Other planar chiral bidentate ligands, again based upon organometallic skeletons, are reviewed in O. Delacroix and J. A. Gladysz, Chem. Commun., 2003, 665.
    • (2003) Chem. Commun. , pp. 665
    • Delacroix, O.1    Gladysz, J.A.2
  • 15
    • 0142173066 scopus 로고
    • This reagent has been used to electrophilically aminate ferrocenyl-lithium to give aminoferrocene in 13% yield, (a) A. N. Nesmeyanov, E. G. Perevalova, R. V. Golovnya and L. S. Shilovtseva, Dokl. Akad. Nauk. SSSR, 1955, 102, 353; (b) G. R. Knox, P. L. Pauson and D. Willison, Organometallics, 1990, 9, 301 and references therein.
    • (1955) Dokl. Akad. Nauk. SSSR , vol.102 , pp. 353
    • Nesmeyanov, A.N.1    Perevalova, E.G.2    Golovnya, R.V.3    Shilovtseva, L.S.4
  • 16
    • 0025388180 scopus 로고
    • and references therein
    • This reagent has been used to electrophilically aminate ferrocenyl-lithium to give aminoferrocene in 13% yield, (a) A. N. Nesmeyanov, E. G. Perevalova, R. V. Golovnya and L. S. Shilovtseva, Dokl. Akad. Nauk. SSSR, 1955, 102, 353; (b) G. R. Knox, P. L. Pauson and D. Willison, Organometallics, 1990, 9, 301 and references therein.
    • (1990) Organometallics , vol.9 , pp. 301
    • Knox, G.R.1    Pauson, P.L.2    Willison, D.3
  • 35
    • 0001038733 scopus 로고    scopus 로고
    • For reviews see: (a) J. P. Wolfe, S. Wagaw, J.-F. Marcoux and S. L. Buchwald, Acc. Chem. Res., 1998, 31, 805; (b) J. F. Hartwig, Angew. Chem., Int. Ed. Engl., 1998, 37, 2046; (c) F. F. Hartwig, Acc. Chem. Res., 1998, 31, 852; (d) B. H. Yang and S. L. Buchwald, J. Organomet. Chem., 1999, 576, 125.
    • (1998) Acc. Chem. Res. , vol.31 , pp. 805
    • Wolfe, J.P.1    Wagaw, S.2    Marcoux, J.-F.3    Buchwald, S.L.4
  • 36
    • 0032541260 scopus 로고    scopus 로고
    • For reviews see: (a) J. P. Wolfe, S. Wagaw, J.-F. Marcoux and S. L. Buchwald, Acc. Chem. Res., 1998, 31, 805; (b) J. F. Hartwig, Angew. Chem., Int. Ed. Engl., 1998, 37, 2046; (c) F. F. Hartwig, Acc. Chem. Res., 1998, 31, 852; (d) B. H. Yang and S. L. Buchwald, J. Organomet. Chem., 1999, 576, 125.
    • (1998) Angew. Chem., Int. Ed. Engl. , vol.37 , pp. 2046
    • Hartwig, J.F.1
  • 37
    • 0000037108 scopus 로고    scopus 로고
    • For reviews see: (a) J. P. Wolfe, S. Wagaw, J.-F. Marcoux and S. L. Buchwald, Acc. Chem. Res., 1998, 31, 805; (b) J. F. Hartwig, Angew. Chem., Int. Ed. Engl., 1998, 37, 2046; (c) F. F. Hartwig, Acc. Chem. Res., 1998, 31, 852; (d) B. H. Yang and S. L. Buchwald, J. Organomet. Chem., 1999, 576, 125.
    • (1998) Acc. Chem. Res. , vol.31 , pp. 852
    • Hartwig, F.F.1
  • 38
    • 0008165462 scopus 로고    scopus 로고
    • For reviews see: (a) J. P. Wolfe, S. Wagaw, J.-F. Marcoux and S. L. Buchwald, Acc. Chem. Res., 1998, 31, 805; (b) J. F. Hartwig, Angew. Chem., Int. Ed. Engl., 1998, 37, 2046; (c) F. F. Hartwig, Acc. Chem. Res., 1998, 31, 852; (d) B. H. Yang and S. L. Buchwald, J. Organomet. Chem., 1999, 576, 125.
    • (1999) J. Organomet. Chem. , vol.576 , pp. 125
    • Yang, B.H.1    Buchwald, S.L.2
  • 44
    • 0142173063 scopus 로고    scopus 로고
    • note
    • Noticeable decomposition did occur after 2 days in air at room temperature.
  • 45
    • 0033455625 scopus 로고    scopus 로고
    • Other hydroxyferrocenes are known where a neighbouring group can participate in hydrogen bonding: T. E. Pickett and C. J. Richards, Tetrahedron: Asymmetry, 1999, 10, 4095.
    • (1999) Tetrahedron: Asymmetry , vol.10 , pp. 4095
    • Pickett, T.E.1    Richards, C.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.