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Volumn 53, Issue 2, 2014, Pages 517-520

Kinetic resolution of allyl fluorides by enantioselective allylic trifluoromethylation based on silicon-assisted c-F bond cleavage

Author keywords

allyl fluorides; fluorine; kinetic resolution; organocatalysis; trifluoromethylation

Indexed keywords

ALLYL FLUORIDES; C-F BONDS; ENANTIOSELECTIVE; FLUORINATED COMPOUND; KINETIC RESOLUTION; ORGANOCATALYSIS; TRIFLUOROMETHYLATION;

EID: 84891762919     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201308071     Document Type: Article
Times cited : (81)

References (74)
  • 12
    • 84882268052 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2013, 52, 8214-8264.
    • (2013) Angew. Chem. Int. Ed. , vol.52 , pp. 8214-8264
  • 14
    • 21344465658 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 3974-4001
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 3974-4001
  • 22
    • 81255169452 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 11112-11116
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 11112-11116
  • 26
    • 60149110499 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 1296-1299
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 1296-1299
  • 29
    • 76249094924 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2010, 49, 1123-1127
    • (2010) Angew. Chem. Int. Ed. , vol.49 , pp. 1123-1127
  • 32
    • 84870525028 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 12275-12279.
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 12275-12279
  • 33
    • 79961056153 scopus 로고    scopus 로고
    • see also Ref.[14]
    • Alkyl-substituted compounds with less bulky groups, such as methyl substituents, are poor substrates for this transformation; see:, T. Furukawa, T. Nishimine, E. Tokunaga, K. Hasegawa, M. Shiro, N. Shibata, Org. Lett. 2011, 13, 3972-3975; see also Ref.[14].
    • (2011) Org. Lett. , vol.13 , pp. 3972-3975
    • Furukawa, T.1    Nishimine, T.2    Tokunaga, E.3    Hasegawa, K.4    Shiro, M.5    Shibata, N.6
  • 37
    • 70349908279 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 6324-6327
    • (2009) Angew. Chem. Int. Ed. , vol.48 , pp. 6324-6327
  • 42
    • 22144453934 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 4204-4207
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 4204-4207
  • 44
  • 49
    • 80053558003 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 9684-9688.
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 9684-9688
  • 61
    • 84891762096 scopus 로고    scopus 로고
    • CCDC959849 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre
    • CCDC959849 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 62
  • 64
    • 47049110210 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 4157-4161
    • (2008) Angew. Chem. Int. Ed. , vol.47 , pp. 4157-4161
  • 68
    • 80052851561 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2011, 50, 9120-9123
    • (2011) Angew. Chem. Int. Ed. , vol.50 , pp. 9120-9123
  • 73
    • 84860760651 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2012, 51, 4577-4580
    • (2012) Angew. Chem. Int. Ed. , vol.51 , pp. 4577-4580


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.