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Volumn 8, Issue 7, 2010, Pages 1497-1504

Asymmetric Si-O coupling of alcohols

Author keywords

[No Author keywords available]

Indexed keywords

CHIRAL ALCOHOLS; CHIRAL SILANES; STEREO-SELECTIVE;

EID: 77949779992     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b925722e     Document Type: Article
Times cited : (88)

References (55)
  • 6
    • 38049036289 scopus 로고    scopus 로고
    • We will not discuss asymmetric hydrosilylations of ketones, as they have been reviewed recently to a certain extent:
    • S. Rendler M. Oestreich Angew. Chem., Int. Ed. 2008 47 248 250
    • (2008) Angew. Chem., Int. Ed. , vol.47 , pp. 248-250
    • Rendler, S.1    Oestreich, M.2
  • 9
    • 0009211057 scopus 로고
    • G. Larson, JAI Press, Greenwich, vol. 1, 327-387
    • For a tabulated summary on transition metal-catalysed Si-O bond formations, see: J. Y. Corey, in Advances in Silicon Chemistry, ed., G. Larson, JAI Press, Greenwich, vol. 1, 1991, pp. 327-387
    • (1991) Advances in Silicon Chemistry
    • Corey, J.Y.1
  • 10
    • 0000482723 scopus 로고
    • For a diastereoselective Si-O coupling using dihydrosilyl ethers with a chiral backbone, see:
    • R. J. P. Corriu J. J. E. Moreau J. Organomet. Chem. 1976 120 337 346
    • (1976) J. Organomet. Chem. , vol.120 , pp. 337-346
    • Corriu, R.J.P.1    Moreau, J.J.E.2
  • 39
    • 29344469998 scopus 로고    scopus 로고
    • Actually, this chemistry was used for the synthesis of optically active polysiloxanes in 2000, yielding an average ee of up to 40% in the polymer, again determined by cleavage of the Si-O bond using MeMgBr:
    • M. Oestreich Chem.-Eur. J. 2006 12 30 37
    • (2006) Chem.-Eur. J. , vol.12 , pp. 30-37
    • Oestreich, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.