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Volumn 132, Issue 48, 2010, Pages 17074-17076

Design of structurally rigid trans -diamine-based Tf-amide organocatalysts with a dihydroanthracene framework for asymmetric conjugate additions of heterosubstituted aldehydes to vinyl sulfones

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC CONJUGATE ADDITION; DIHYDROANTHRACENE; HIGH ENANTIOSELECTIVITY; ORGANOCATALYSTS; VINYL SULFONES;

EID: 78650082407     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja107897t     Document Type: Article
Times cited : (60)

References (46)
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    • Recent reviews on asymmetric aminocatalysis
    • Recent reviews on asymmetric aminocatalysis
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    • 0034750244 scopus 로고    scopus 로고
    • List, B. Synlett 2001, 11, 1675
    • (2001) Synlett , vol.11 , pp. 1675
    • List, B.1
  • 7
    • 78650109491 scopus 로고    scopus 로고
    • Reviews on asymmetric aminocatalysis by primary amino acids
    • Reviews on asymmetric aminocatalysis by primary amino acids
  • 17
    • 78650102583 scopus 로고    scopus 로고
    • Recent reviews on α,α-dialkylated amino acids
    • Recent reviews on α,α-dialkylated amino acids
  • 21
    • 0038391041 scopus 로고    scopus 로고
    • Previous examples of chiral α,α-dialkylamino aldehyde synthesis:, Eur. J. Org. Chem. 2008, 13, 2207
    • Ohfune, Y. and Shinada, T. Bull. Chem. Soc. Jpn. 2003, 76, 1115 Previous examples of chiral α,α-dialkylamino aldehyde synthesis: Baumann, T., Baechle, M., Hartmann, C., and Braese, S. Eur. J. Org. Chem. 2008, 13, 2207
    • (2003) Bull. Chem. Soc. Jpn. , vol.76 , pp. 1115
    • Ohfune, Y.1    Shinada, T.2    Baumann, T.3    Baechle, M.4    Hartmann, C.5    Braese, S.6
  • 30
    • 78650160199 scopus 로고    scopus 로고
    • For preparation of (S, S)- 3, see
    • For preparation of (S, S)- 3, see
  • 33
    • 78650132149 scopus 로고    scopus 로고
    • Preparation of α-amino-substituted aldehydes 5a - i
    • Preparation of α-amino-substituted aldehydes 5a - i
  • 36
    • 78650119960 scopus 로고    scopus 로고
    • Use of 1,1-bis(benzenesulfonyl)ethylene for the generation of quaternary carbon centers
    • Use of 1,1-bis(benzenesulfonyl)ethylene for the generation of quaternary carbon centers
  • 45
    • 78650153852 scopus 로고    scopus 로고
    • Asymmetric conjugate addition of 5i at -20 °C for 72 h gave 6i in 98% yield with 80% ee
    • Asymmetric conjugate addition of 5i at -20 °C for 72 h gave 6i in 98% yield with 80% ee.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.