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Volumn 7, Issue 19, 2005, Pages 4293-4296

Chiral binaphthyl-derived amine-thiourea organocatalyst-promoted asymmetric Morita-Baylis-Hillman reaction

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDE; AMINE; NAPHTHALENE DERIVATIVE; THIOUREA;

EID: 25444432564     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol051822+     Document Type: Article
Times cited : (274)

References (47)
  • 15
    • 15744383666 scopus 로고    scopus 로고
    • aza-MBH reactions also have been studied; for selected examples, see: (a) Shi, M.; Chen, L.-H.; Li, C.-Q. J. Am. Chem. Soc. 2005, 127, 3790.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 3790
    • Shi, M.1    Chen, L.-H.2    Li, C.-Q.3
  • 29
    • 15244343428 scopus 로고    scopus 로고
    • For recent reviews related to use of ureas/thioureas as organocatalysts for organic reactions, see: (a) Seayad, J.; List, B. Org. Biomol. Chem. 2005, 3, 719.
    • (2005) Org. Biomol. Chem. , vol.3 , pp. 719
    • Seayad, J.1    List, B.2
  • 31
    • 0003554758 scopus 로고    scopus 로고
    • For selected examples using ureas/thioureas as catalysts in asymmetric organic transformations, see: (a) Sigman, M. S.; Jacobsen, E. N. J. Am. Chem. Soc. 1998, 120, 4901.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 4901
    • Sigman, M.S.1    Jacobsen, E.N.2
  • 43
    • 0037436454 scopus 로고    scopus 로고
    • For a review of "privileged" structures in catalysis, see: Yoon, T. P.; Jacobsen, E. N. Science 2003, 299, 1691.
    • (2003) Science , vol.299 , pp. 1691
    • Yoon, T.P.1    Jacobsen, E.N.2
  • 47
    • 25444457966 scopus 로고    scopus 로고
    • note
    • 3 (v/v, 1/9) 80% yield, 63% ee; 1,4-dioxane 61% yield, 77% ee; and DMF 38% yield, 61% ee.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.