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Volumn , Issue , 2007, Pages 250-277

Catalytic Asymmetric Synthesis: The QUINAPHOS Ligand Family and its Application in Asymmetric Catalysis

Author keywords

Allylic alkylation; Asymmetric synthesis; Chemical methods; Enantioselective catalysis; Immobilization of transition metal complexes; Oxygen nucleophiles; QUINAPHOS ligand family; Sulfur nucleophiles

Indexed keywords


EID: 34347333207     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9783527610648.ch2b     Document Type: Chapter
Times cited : (7)

References (108)
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    • Comprehensive Asymmetric Catalysis (E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Eds.), Springer: Berlin, 2004.
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  • 35
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    • Christiane J. Diez-Holz, Diploma Thesis, University of Aachen (Germany), 2005
    • Christiane J. Diez-Holz, Diploma Thesis, University of Aachen (Germany), 2005.
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    • C. J. Diez-Holz, C. Boeing, J. Klankermayer, M. Hoelscher, G. Franciò, W. Leitner, in preparation
    • C. J. Diez-Holz, C. Boeing, J. Klankermayer, M. Hoelscher, G. Franciò, W. Leitner, in preparation.
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    • G. Franciò, PhD Thesis, University of Messina (Italy), 2000
    • G. Franciò, PhD Thesis, University of Messina (Italy), 2000.
  • 38
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    • A similar arrangement was found for a rhodium complex based on the phosphine-phosphite BINAPHOS ligand: see ref. [26a]
    • A similar arrangement was found for a rhodium complex based on the phosphine-phosphite BINAPHOS ligand: see ref. [26a].
  • 47
    • 24944547484 scopus 로고    scopus 로고
    • A renewed interest in asymmetric hydroformylation driven by academic, industrial research laboratories as well recently enabled significant progress to be made in this synthetically extremely useful transformation.See
    • A renewed interest in asymmetric hydroformylation driven by academic and industrial research laboratories as well recently enabled significant progress to be made in this synthetically extremely useful transformation. See: (a) A. T. Axtell, C. J. Cobley, J. Klosin, G. T. Whiteker, A. Zanotti-Gerosa, K. A. Abboud, Angew. Chem. Int. Ed. 2005, 44, 5834;
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 5834
    • Axtell, A.T.1    Cobley, C.J.2    Klosin, J.3    Whiteker, G.T.4    Zanotti-Gerosa, A.5    Abboud, K.A.6
  • 53
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    • Simon Burk, Diploma Thesis, University of Aachen (Germany), 2004
    • Simon Burk, Diploma Thesis, University of Aachen (Germany), 2004.
  • 59
    • 33444462389 scopus 로고
    • For the first asymmetric hydrogenation using monodentate P-ligands see
    • For the first asymmetric hydrogenation using monodentate P-ligands see: (a) W. S. Knowles, M. J. Sabacky, Chem. Commun. 1968, 1445;
    • (1968) Chem. Commun. , pp. 1445
    • Knowles, W.S.1    Sabacky, M.J.2
  • 75
    • 0000554241 scopus 로고    scopus 로고
    • Applied Homogeneous Catalysis with Organometallic Compounds
    • For recent reviews see, (B. Cornils, W. A. Herrmann, Eds.), VCH, New York
    • For recent reviews see: (a) P. W. Jolly, G. Wilke, in Applied Homogeneous Catalysis with Organometallic Compounds (B. Cornils, W. A. Herrmann, Eds.), VCH, New York, 1996; Vol. 2, p. 1024;
    • (1996) , vol.2 , pp. 1024
    • Jolly, P.W.1    Wilke, G.2
  • 103
    • 13444308668 scopus 로고
    • The synthesis of the [Ni(allyl)(cod)][Y] complexes was accomplished by following the procedures in
    • The synthesis of the [Ni(allyl)(cod)][Y] complexes was accomplished by following the procedures in: (a) R. B. A. Pardy, I. Tkatschenko, J. Chem. Soc., Chem. Commun. 1981, 49;
    • (1981) J. Chem. Soc., Chem. Commun. , pp. 49
    • Pardy, R.B.A.1    Tkatschenko, I.2
  • 105
    • 84890995387 scopus 로고    scopus 로고
    • [Ni(allyl)(cod)][BARF] as the catalyst without a P ligand led to 7% conversion and 22%regioselectivity within 24 h
    • [Ni(allyl)(cod)][BARF] as the catalyst without a P ligand led to 7% conversion and 22%regioselectivity within 24 h.
  • 106
    • 84891017705 scopus 로고    scopus 로고
    • See footnote [a] in Table 2.1.5.1
    • See footnote [a] in Table 2.1.5.1.
  • 107
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    • For a recent review on weakly coordinating anions see
    • For a recent review on weakly coordinating anions see: I. Krossing, I. Raabe, Angew. Chem. Int. Ed. 2004, 43, 2066.
    • (2004) Angew. Chem. Int. Ed. , vol.43 , pp. 2066
    • Krossing, I.1    Raabe, I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.