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Volumn 133, Issue , 2012, Pages 102-107

Regiospecific and diastereoselective aldol reaction of chiral N-sulfinyl metalloenamines with α,β-unsaturated trifluoromethyl ketones: Asymmetric synthesis of tertiary trifluoromethyl allylic carbinols

Author keywords

, Unsaturated trifluoromethyl ketone; Asymmetric synthesis; N Sulfinyl metalloenamine; Tertiary trifluoromethyl allylic carbinol

Indexed keywords


EID: 84655169104     PISSN: 00221139     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jfluchem.2011.09.002     Document Type: Article
Times cited : (12)

References (44)
  • 9
    • 11144341001 scopus 로고    scopus 로고
    • the update: Chem. Rev. 108 (2008) PR1-PR43
    • J.-A. Ma, and D. Cahard Chem. Rev. 104 2004 6119 6146 and the update: Chem. Rev. 108 (2008) PR1-PR43
    • (2004) Chem. Rev. , vol.104 , pp. 6119-6146
    • Ma, J.-A.1    Cahard, D.2
  • 13
    • 0026530301 scopus 로고
    • For the asymmetric synthesis of secondary trifluoromethyl allylic alcohols, see: (a) T. Kubota, M. Yamamoto, Tetrahedron Lett. 33 (1992) 2603-2606
    • (1992) Tetrahedron Lett. , vol.33 , pp. 2603-2606
    • Kubota, T.1    Yamamoto, M.2
  • 18
    • 0000096529 scopus 로고    scopus 로고
    • For the racemic synthesis of tertiary trifluoromethyl allylic alcohols, see
    • For the racemic synthesis of tertiary trifluoromethyl allylic alcohols, see: R.P. Singh, R.L. Kirchmeier, and J.M. Shreeve Org. Lett. 1 1999 1047 1049
    • (1999) Org. Lett. , vol.1 , pp. 1047-1049
    • Singh, R.P.1    Kirchmeier, R.L.2    Shreeve, J.M.3
  • 42
    • 0027371339 scopus 로고
    • For example of the 1,4-addition of organometallic reagents to α,β-unsaturated trifluoromethyl ketones, see
    • For example of the 1,4-addition of organometallic reagents to α,β-unsaturated trifluoromethyl ketones, see: E. Takada, S. Hara, and A. Suzuki Tetrahedron Lett. 34 1993 7067 7070
    • (1993) Tetrahedron Lett. , vol.34 , pp. 7067-7070
    • Takada, E.1    Hara, S.2    Suzuki, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.