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Volumn 16, Issue 5, 2010, Pages 1638-1645

Chiral brønsted acid directed iron-catalyzed enantioselective friedelcrafts alkylation of indoles with β-aryl α'-hydroxy enones

Author keywords

Alkylation; Asymmetric catalysis; Br nsted acids; Iron; Proton acceleration

Indexed keywords

ASYMMETRIC CATALYSIS; BASIC SITES; CATALYTIC ACTIVITY; CATALYTIC SPECIES; CATALYTIC SYSTEM; COOPERATIVE CATALYTIC SYSTEMS; ENANTIOSELECTIVE; ENATIOSELECTIVITIES; FRIEDEL-CRAFTS ALKYLATION; HIGH ACTIVITY; HYDROGEN BONDING INTERACTIONS; HYDROXY ENONES; IRON SALTS; LEWIS-ACID ACTIVATION; PARA POSITION; PHENYL RINGS; PHOSPHATE SALTS; PROTON ACCELERATION; REACTION MECHANISM;

EID: 75749128225     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200902705     Document Type: Article
Times cited : (73)

References (93)
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    • For recent reviews of Friedel-Crafts alkylation reactions, see: a) G. A. Olah, R. Krishnamurti, G. K. S. Prakash, Comprehensive Organic Synthesis, Vol.3, 1st ed. (Eds.: B. M. Trost, I. Fleming), Pergamon, Oxford, 1991, p. 293;
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  • 28
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    • For selected examples of Friedel-Crafts alkylation of indoles with α,β-unsaturated compounds, a
    • For selected examples of Friedel-Crafts alkylation of indoles with α,β-unsaturated compounds, see: a) W. Zhuang, T. Hansen, K. A. Jørgensen, Chem. Commun. 2001, 347;
    • (2001) Chem. Commun. , pp. 347
    • Zhuang, W.1    Hansen, T.2    Jørgensen, K.A.3
  • 64
    • 11144323895 scopus 로고    scopus 로고
    • For selected reviews of iron-catalyzed organic reactions, a
    • For selected reviews of iron-catalyzed organic reactions, see: a) C. Bolm, J. Legros, J. Le Paih, L. Zani, Chem. Rev. 2004, 104, 6217;
    • (2004) Chem. Rev. , vol.104 , pp. 6217
    • Bolm, C.1    Legros, J.2    Le Paih, J.3    Zani, L.4
  • 78
    • 75749124037 scopus 로고    scopus 로고
    • 3, only low ee values were obtained (-2O0C, 48 h, 80% yield, 18% ee).
    • 3, only low ee values were obtained (-2O0C, 48 h, 80% yield, 18% ee).
  • 90
    • 42449110313 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 2458. also see:
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 2458


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.