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Volumn 1, Issue 3, 2011, Pages 389-392

Organocatalytic asymmetric Henry reaction of isatins: Highly enantioselective synthesis of 3-hydroxy-2-oxindoles

Author keywords

[No Author keywords available]

Indexed keywords

CINCHONA ALKALOID; ENANTIOSELECTIVE SYNTHESIS; HENRY REACTIONS; HIGH ENANTIOSELECTIVITY; NITROMETHANE; ORGANOCATALYTIC; TOTAL SYNTHESIS;

EID: 84856379158     PISSN: None     EISSN: 20462069     Source Type: Journal    
DOI: 10.1039/c1ra00477h     Document Type: Article
Times cited : (54)

References (53)
  • 48
    • 67649380750 scopus 로고    scopus 로고
    • 828228 Crystal data for 3g: C9H7BrN 2O4, M = 287.08, monoclinic, a = 7.437(15) Å, b = 6.480(13) Å, c = 10.87(2) Å, α = 90.00°, β = 90.185(17)°, γ = 90.00°, V = 523.6(18) Å3, T = 296(2)K, space group P21, Z = 2, 3567 reflections measured, 1895 independent reflections (Rint = 0.0669). The final R1 values were 0.0488 (I > 2σ(I)). The final wR(F2) values were 0.1074 (I > 2σ(I)). The final R1 values were 0.0776 (all data). The final wR(F2) values were 0.1191 (all data). Supplementary crystallographic data have been deposited at the Cambridge Crystallographic Data Centre, CCDC For the isolation of (R)-(+)-dioxibrassinin, see
    • X. Liu B. Sun L. Deng Synlett 2009 1685
    • Synlett , vol.2009 , pp. 1685
    • Liu, X.1    Sun, B.2    Deng, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.