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Volumn 2, Issue 4, 2010, Pages 375-378

Enantioselective 6π Electrocyclizations: Pushing the Limits in Organocatalytic Pericyclic Reactions

Author keywords

Asymmetric synthesis; Electrocyclic reactions; Heterocyclic compounds; Organocatalysis; Stereoselective catalysis

Indexed keywords


EID: 77953856581     PISSN: 18673880     EISSN: 18673899     Source Type: Journal    
DOI: 10.1002/cctc.200900324     Document Type: Article
Times cited : (17)

References (30)
  • 13
    • 58249120683 scopus 로고    scopus 로고
    • For an example of a Lewis-acid catalyzed hexatriene 6π electrocyclization see
    • D. J. Tantillo, Angew. Chem. Int. Ed. 2009, 48, 31, For an example of a Lewis-acid catalyzed hexatriene 6π electrocyclization see
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 31
    • Tantillo, D.J.1
  • 15
    • 54049095251 scopus 로고    scopus 로고
    • For an example of a Lewis-acid catalyzed pentadienyl anion cyclization, see.
    • L. M. Bishop, J. E. Barbarow, R. G. Bergman, D. Trauner, Angew. Chem. Int. Ed. 2008, 47, 8100; For an example of a Lewis-acid catalyzed pentadienyl anion cyclization, see.
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 8100
    • Bishop, L.M.1    Barbarow, J.E.2    Bergman, R.G.3    Trauner, D.4
  • 16
    • 0011005798 scopus 로고
    • For a recent example of a thermal 6π-azaelectrocyclizationm, see.
    • J. Dijkink, J. N. Zonjee, B. S. de Jong, W. N. Speckamp, Heterocycles 1983, 20, 1255; For a recent example of a thermal 6π-azaelectrocyclizationm, see.
    • (1983) Heterocycles , vol.20 , pp. 1255
    • Dijkink, J.1    Zonjee, J.N.2    de Jong, B.S.3    Speckamp, W.N.4
  • 20
    • 36949016625 scopus 로고    scopus 로고
    • For a recent review on asymmetric phase-transfer catalysis, see
    • For a recent review on asymmetric phase-transfer catalysis, see: T. Ooi, K. Maruoka, Angew. Chem. 2007, 119, 4300
    • (2007) Angew. Chem. , vol.119 , pp. 4300
    • Ooi, T.1    Maruoka, K.2
  • 25
    • 79957759657 scopus 로고    scopus 로고
    • For one example of a Ni-catalyzed asymmetric cascade conjugate addition-cyclocondensation of enones with arylhydrazines proceeding with moderate enantioselectivities, see.
    • For one example of a Ni-catalyzed asymmetric cascade conjugate addition-cyclocondensation of enones with arylhydrazines proceeding with moderate enantioselectivities, see.
  • 26
    • 34547095984 scopus 로고    scopus 로고
    • For a racemic organocatalytic version, see.
    • H. Yanagita, S. Kanemasa, Heterocycles 2007, 71, 699; For a racemic organocatalytic version, see.
    • (2007) Heterocycles , vol.71 , pp. 699
    • Yanagita, H.1    Kanemasa, S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.