메뉴 건너뛰기




Volumn , Issue 10, 2013, Pages 1902-1907

Enantioselective friedel-crafts alkylation of indoles with (e)-1-aryl-4-benzyloxybut-2-en-1-ones catalyzed by an (R)-3,3′-Br 2BINOLate-Hafnium(IV) complex

Author keywords

Alkylation; Asymmetric catalysis; C C coupling; Hafnium; Regioselectivity

Indexed keywords


EID: 84875463455     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201201636     Document Type: Article
Times cited : (11)

References (84)
  • 1
    • 84875474714 scopus 로고    scopus 로고
    • For examples of relevant natural products and potential medicinal agents, see
    • For examples of relevant natural products and potential medicinal agents, see
  • 17
    • 84875426884 scopus 로고    scopus 로고
    • For a review on Friedel-Crafts reactions, see
    • For a review on Friedel-Crafts reactions, see
  • 18
    • 0001586671 scopus 로고
    • in Comprehensive Organic Synthesis (Eds.:, Pergamon Press, Oxford, 293-339. For reviews on enantioselective Friedel-Crafts reactions, see
    • G. A. Olah, R. Krishnamurti, G. K. S. Prakash, Friedel-Crafts Alkylations, in Comprehensive Organic Synthesis (Eds.:, B. M. Trost, I. Fleming), Pergamon Press, Oxford, 1991, vol. 3, pp. 293-339. For reviews on enantioselective Friedel-Crafts reactions, see
    • (1991) Friedel-Crafts Alkylations
    • Olah, G.A.1    Krishnamurti, R.2    Prakash, G.K.S.3    Trost, B.M.4    Fleming, I.5
  • 19
  • 20
    • 84891005153 scopus 로고    scopus 로고
    • Catalytic Asymmetric Friedel-Crafts Alkylations (Eds.:, Wiley-VCH, Weinheim, Germany.
    • Catalytic Asymmetric Friedel-Crafts Alkylations (Eds.:, M. Bandini, A. Umani-Ronchi), Wiley-VCH, Weinheim, Germany, 2009.
    • (2009)
    • Bandini, M.1    Umani-Ronchi, A.2
  • 22
    • 71949117774 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 9608 - 9644.
    • M. Bandini, A. Eichholzer, Angew. Chem. 2009, 121, 9786; Angew. Chem. Int. Ed. 2009, 48, 9608-9644.
    • (2009) Angew. Chem. , vol.121 , pp. 9786
    • Bandini, M.1    Eichholzer, A.2
  • 39
    • 70349683306 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 9913 -9915.
    • M. P. Sibi, J. Coulomb, L. M. Stanley, Angew. Chem. 2008, 120, 10061-10063; Angew. Chem. Int. Ed. 2008, 47, 9913 -9915.
    • (2008) Angew. Chem. , vol.120 , pp. 10061-10063
    • Sibi, M.P.1    Coulomb, J.2    Stanley, L.M.3
  • 40
    • 73349095277 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 3346 -3348.
    • A. J. Boersma, B. L. Feringa, G. Roelfes, Angew. Chem. 2009, 121, 3396-3398; Angew. Chem. Int. Ed. 2009, 48, 3346 -3348.
    • (2009) Angew. Chem. , vol.121 , pp. 3396-3398
    • Boersma, A.J.1    Feringa, B.L.2    Roelfes, G.3
  • 49
    • 56449087939 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 4016 -4018.
    • J. Itoh, K. Fuchibe, T. Akiyama, Angew. Chem. 2008, 120, 4080-4082; Angew. Chem. Int. Ed. 2008, 47, 4016 -4018.
    • (2008) Angew. Chem. , vol.120 , pp. 4080-4082
    • Itoh, J.1    Fuchibe, K.2    Akiyama, T.3
  • 62
    • 77149175767 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 7428 -7431.
    • Q. Cai, Z.-A. Zhao, S.-L. You, Angew. Chem. 2009, 121, 7564-7567; Angew. Chem. Int. Ed. 2009, 48, 7428 -7431.
    • (2009) Angew. Chem. , vol.121 , pp. 7564-7567
    • Cai, Q.1    Zhao, Z.-A.2    You, S.-L.3
  • 65
    • 84875453254 scopus 로고    scopus 로고
    • The (E)-1-aryl-4-benzyloxybut-2-en-1-ones (2) were synthesized by aldol reaction followed by dehydratation, see the Supporting Information
    • The (E)-1-aryl-4-benzyloxybut-2-en-1-ones (2) were synthesized by aldol reaction followed by dehydratation, see the Supporting Information.
  • 68
    • 84875409073 scopus 로고    scopus 로고
    • CCDC-911096 (for 3bf) contains the supplementary crystallographic data. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC-911096 (for 3bf) contains the supplementary crystallographic data. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 77
    • 84875428433 scopus 로고    scopus 로고
    • For reviews on bifunctional catalysts, see
    • For reviews on bifunctional catalysts, see
  • 78
    • 0000218541 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. Engl. 1997, 36, 1236 -1256.
    • M. Shibasaki, H. Sasai, T. Arai, Angew. Chem. 1997, 109, 1290-1311; Angew. Chem. Int. Ed. Engl. 1997, 36, 1236 -1256.
    • (1997) Angew. Chem. , vol.109 , pp. 1290-1311
    • Shibasaki, M.1    Sasai, H.2    Arai, T.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.