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Volumn 37, Issue 35, 1996, Pages 6359-6362

Diastereoselective synthesis of axially chiral biaryls via nucleophilic addition to (arene)chromium complexes with Grignard reagents

Author keywords

[No Author keywords available]

Indexed keywords

BIPHENYL DERIVATIVE;

EID: 0030603040     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01371-8     Document Type: Article
Times cited : (20)

References (27)
  • 2
    • 0000182592 scopus 로고
    • Asymmetric synthesis via chiral oxazolines
    • Morison, J. D.; Ed.; Academic Press, Inc.: New York
    • (b) Lutomski, K. A.; Meyers, A. I. "Asymmetric Synthesis via Chiral Oxazolines". In Asymmetric Synthesis; Morison, J. D.; Ed.; Academic Press, Inc.: New York, 1984, Vol. 3, pp. 213-274.
    • (1984) Asymmetric Synthesis , vol.3 , pp. 213-274
    • Lutomski, K.A.1    Meyers, A.I.2
  • 11
    • 0000747080 scopus 로고
    • Wilkinsons, G.; Stone, P. G. A.; Abel, E. W. Eds.; Pergamon Press: Oxford
    • 3 (a) Semmelhack, M. F. In "Comprehensive Organometallic Chemistry II", Wilkinsons, G.; Stone, P. G. A.; Abel, E. W. Eds.; Pergamon Press: Oxford, 1995, Vol. 12, pp. 979-1015.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 979-1015
    • Semmelhack, M.F.1
  • 16
    • 0030010394 scopus 로고    scopus 로고
    • 5 Planar chirality of cyclophane is converted to axial chirality of binaphthyls by nucleophilic addition of aryl Grignard: Hattori, T.; Koike, N.; Okaishi, Y.; Miyano, S. Tetrahedron Lett. 1996, 37, 2057-2060.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 2057-2060
    • Hattori, T.1    Koike, N.2    Okaishi, Y.3    Miyano, S.4
  • 17
    • 85030270666 scopus 로고    scopus 로고
    • note
    • 3) δ 1.88 (3H, s), 1.96 (6H, s), 2.08 (3H, s), 2.19 (3H, s), 5.36 (1H, d, J = 6.4 Hz), 5.67 (1H, t, J = 6.4 Hz), 5.97 (1H, d, J = 6.4 Hz), 6.77 (2H, s), 7.16-7.26 (3H, m), 7.49 (1H, dd, J = 6.3, 7.1 Hz).
  • 23
    • 0027458113 scopus 로고
    • and references cited there in
    • 9 It is well known that the ortho oxygen on aryl Grignards can easily coordinate with magnesium in the enolate intermediate of the reaction with chiral aryloxazolines: Moorlag, H.; Meyers, A. I. Tetrahedron Lett. 1993, 34, 6989-6992 and references cited there in.
    • (1993) Tetrahedron Lett. , vol.34 , pp. 6989-6992
    • Moorlag, H.1    Meyers, A.I.2
  • 27
    • 85030279951 scopus 로고    scopus 로고
    • 4c
    • 4c


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.