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Volumn 124, Issue 45, 2002, Pages 13396-13397

Nickel-catalyzed asymmetric Grignard cross-coupling of dinaphthothiophene giving axially chiral 1,1′-binaphthyls

Author keywords

[No Author keywords available]

Indexed keywords

1,1' BINAPHTHYL DERIVATIVE; CARBON; NICKEL; SULFUR; THIOPHENE DERIVATIVE;

EID: 0037073236     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0282588     Document Type: Article
Times cited : (123)

References (33)
  • 3
    • 0000718373 scopus 로고    scopus 로고
    • (c) Pu, L. Chem. Rev. 1998, 98, 2405.
    • (1998) Chem. Rev. , vol.98 , pp. 2405
    • Pu, L.1
  • 6
    • 0011133958 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, Chapter 25
    • (a) Hayashi, T. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, 1999; Vol. II, Chapter 25.
    • (1999) Comprehensive Asymmetric Catalysis , vol.2
    • Hayashi, T.1
  • 25
    • 0011152270 scopus 로고    scopus 로고
    • note
    • 2 can be used as well, although the reaction rate is a little slower.
  • 26
    • 0011145735 scopus 로고    scopus 로고
    • note
    • THF is a solvent of choice because the dinaphthothiophene 1 is not soluble in other solvents (benzene, toluene, or diethyl ether) usually used for the Grignard cross-coupling.
  • 29
    • 0033603883 scopus 로고    scopus 로고
    • The oxidative addition of a dibenzothiophene to a nickel species forming a nickelacycle complex has been reported: Vicic, D. A.; Jones, W. D. J. Am. Chem. Soc. 1999, 121, 7606.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 7606
    • Vicic, D.A.1    Jones, W.D.2
  • 30
    • 0011118282 scopus 로고    scopus 로고
    • note
    • D +145 (c 1.0, chloroform)) of the authentic sample prepared from -binaphthol (ref 12).
  • 32
    • 0011154845 scopus 로고    scopus 로고
    • note
    • The MOP ligand 15 is useful as a chiral ligand for the palladium-catalyzed asymmetric hydrosilylation of 1,3-dienes (ref 12).
  • 33
    • 0032917881 scopus 로고    scopus 로고
    • Similar asymmetric ring-opening reactions of biaryl lactones have been studied extensively by Bringmann: Bringmann, G.; Breuning, M.; Tasler, S. Synthesis 1999, 525.
    • (1999) Synthesis , pp. 525
    • Bringmann, G.1    Breuning, M.2    Tasler, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.