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Volumn 74, Issue 17, 2009, Pages 6878-6880

Highly efficient asymmetric synthesis of 3-indolyl(hydroxy)acetates via Friedel-Crafts alkylation of indoles

Author keywords

[No Author keywords available]

Indexed keywords

ASYMMETRIC SYNTHESIS; CHEMICAL EQUATIONS; ENANTIOSELECTIVE; ETHYL GLYOXYLATE; FRIEDEL-CRAFTS ALKYLATION; GOOD YIELD; HIGH ENANTIOSELECTIVITY;

EID: 69549128248     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo901425z     Document Type: Article
Times cited : (38)

References (54)
  • 3
    • 0001586671 scopus 로고
    • Friedel-Crafts Alkylations
    • Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, UK
    • (c) Olah G. A.; Krishnamurti, R.; Prakash, G. K. S. Friedel-Crafts Alkylations. In Comprehensive Organic Synthesis; Trost, B. M., Fleming, I., Eds.; Pergamon Press: Oxford, UK, 1991; Vol.3, pp 293-339.
    • (1991) Comprehensive Organic Synthesis , vol.3 , pp. 293-339
    • Olah, G.A.1    Krishnamurti, R.2    Prakash, G.K.S.3
  • 6
    • 4344713238 scopus 로고    scopus 로고
    • For recent reviews of catalytic asymmetric F-C reactions of indoles, see
    • For recent reviews of catalytic asymmetric F-C reactions of indoles, see: (a) Taylor, M. S.; Jacobsen, E. N. J. Am. Chem. Soc. 2004, 126, 10558.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 10558
    • Taylor, M.S.1    Jacobsen, E.N.2
  • 14
  • 20
    • 33846972343 scopus 로고    scopus 로고
    • For catalytic asymmetric F-C reactions of indoles catalyzed by an organic catalyst, see
    • For catalytic asymmetric F-C reactions of indoles catalyzed by an organic catalyst, see: (g) Kang, Q.; Zhao, Z. A.; You, S. L. J. Am. Chem. Soc. 2007, 129, 1484.
    • (2007) J. Am. Chem. Soc. , vol.129 , pp. 1484
    • Kang, Q.1    Zhao, Z.A.2    You, S.L.3
  • 22
    • 0033533951 scopus 로고    scopus 로고
    • For catalytic asymmetric 1,2-nucleophilic additions of indoles, see
    • For catalytic asymmetric 1,2-nucleophilic additions of indoles, see: (a) Johannsen, M. Chem. Commun. 1999, 2233.
    • (1999) Chem. Commun. , pp. 2233
    • Johannsen, M.1
  • 53
    • 6344249037 scopus 로고    scopus 로고
    • The additives often change the reactivity and enantioselectivity in chiral Lewis acid catalyzed reaction
    • The additives often change the reactivity and enantioselectivity in chiral Lewis acid catalyzed reaction: (a) Bandini, M.; Fagioli, P.; Garavelli, M.; Melloni, A.; Trigari, V.; Umani-Ronchi, A. J. Org. Chem. 2004, 69, 7511.
    • (2004) J. Org. Chem. , vol.69 , pp. 7511
    • Bandini, M.1    Fagioli, P.2    Garavelli, M.3    Melloni, A.4    Trigari, V.5    Umani-Ronchi, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.