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Volumn 53, Issue 49, 1997, Pages 16663-16678

General method for asymmetric synthesis of substituted 2,2'-biaryldiols via asymmetric desymmetrization of 2,2',6,6'-tetrahydroxybiphenyl with l- menthone

Author keywords

[No Author keywords available]

Indexed keywords

BIPHENYL DERIVATIVE; MENTHONE; POLYCYCLIC AROMATIC HYDROCARBON DERIVATIVE;

EID: 0030785385     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)10094-1     Document Type: Article
Times cited : (23)

References (56)
  • 3
    • 0001636275 scopus 로고
    • and references cited therein
    • (a) For leading references, see Bao, J.; Wulff, W. D.; Rheingold, A. L. J. Am. Chem. Soc. 1993, 115, 3814 and references cited therein.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 3814
    • Bao, J.1    Wulff, W.D.2    Rheingold, A.L.3
  • 11
    • 0000332467 scopus 로고
    • Helmchen, G.; Hoffmann, R. W. ; Mulzer, J.; Schumann, E., Ed.; Georg Thieme Verlag: Stuttgart
    • (b) Review: Bringmann, G.; Walter, R.; Weirich, R. Methods of Organic Chemistry (Houben-Weyl); Helmchen, G.; Hoffmann, R. W. ; Mulzer, J.; Schumann, E., Ed.; Georg Thieme Verlag: Stuttgart, 1995; Vol. E21a, p 567.
    • (1995) Methods of Organic Chemistry (Houben-Weyl) , vol.E21A , pp. 567
    • Bringmann, G.1    Walter, R.2    Weirich, R.3
  • 35
    • 0006198233 scopus 로고
    • Helmchen, G.; Hoffmann, R. W. ; Mulzer, J.; Schumann, E., Ed.; Georg Thieme Verlag: Stuttgart
    • (c) Gais, H. -J. Methods of Organic Chemistry (Houben-Weyl); Helmchen, G.; Hoffmann, R. W. ; Mulzer, J.; Schumann, E., Ed.; Georg Thieme Verlag: Stuttgart, 1995; Vol. E21a, p 589.
    • (1995) Methods of Organic Chemistry (Houben-Weyl) , vol.E21A , pp. 589
    • Gais, H.-J.1
  • 43
    • 85036682629 scopus 로고    scopus 로고
    • The authors have deposited atomic coordinates for 5a and 6c with the Cambridge Crystallographic Data Centre
    • The authors have deposited atomic coordinates for 5a and 6c with the Cambridge Crystallographic Data Centre.
  • 48
    • 85036683916 scopus 로고    scopus 로고
    • note
    • The mechanism of racemization is still unclear. Although acid catalyzed racemization of BINOL at 100 °C has been reported previously, 16 a separate experiment showed that 13a did not racemize under acidic conditions at rt.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.