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Volumn 14, Issue 9, 2012, Pages 2406-2409

Two-directional desymmetrization by double 1,4-addition of silicon and boron nucleophiles

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EID: 84860621927     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol300832f     Document Type: Article
Times cited : (43)

References (43)
  • 13
    • 33845283382 scopus 로고
    • Kinetic resolution effects might also be considered when asymmetric induction of the used method is not high. For a scholarly example producing a highly enantiomerically enriched monofunctionalized carbinol, see
    • Kinetic resolution effects might also be considered when asymmetric induction of the used method is not high. For a scholarly example producing a highly enantiomerically enriched monofunctionalized carbinol, see: Schreiber, S. L.; Schreiber, T. S.; Smith, D. B. J. Am. Chem. Soc. 1987, 109, 1525-1529
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 1525-1529
    • Schreiber, S.L.1    Schreiber, T.S.2    Smith, D.B.3
  • 14
    • 79959895362 scopus 로고    scopus 로고
    • For a comprehensive overview of asymmetric conjugate addition reactions of silicon and boron nucleophiles, see
    • For a comprehensive overview of asymmetric conjugate addition reactions of silicon and boron nucleophiles, see: Hartmann, E.; Vyas, D. J.; Oestreich, M. Chem. Commun. 2011, 47, 7917-7932
    • (2011) Chem. Commun. , vol.47 , pp. 7917-7932
    • Hartmann, E.1    Vyas, D.J.2    Oestreich, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.