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Volumn 14, Issue 17, 2012, Pages 4374-4377

Enantioselective organocatalyzed sulfenylation of 3-substituted oxindoles

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Indexed keywords


EID: 84866029875     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol301833f     Document Type: Article
Times cited : (74)

References (77)
  • 1
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    • special issue on organocatalysis
    • Acc. Chem. Res. 2004, 37 (8), special issue on organocatalysis.
    • (2004) Acc. Chem. Res. , vol.37 , Issue.8
  • 2
    • 84866044177 scopus 로고    scopus 로고
    • special issue on organocatalysis.
    • Chem. Rev. 2007, 107 (12), special issue on organocatalysis.
    • (2007) Chem. Rev. , vol.107 , Issue.12
  • 3
    • 84866030774 scopus 로고    scopus 로고
    • special feature issue on organocatalysis.
    • Proc. Natl. Acad. Sci. U.S.A. 2010, 107 (48), special feature issue on organocatalysis.
    • (2010) Proc. Natl. Acad. Sci. U.S.A. , vol.107 , Issue.48
  • 61
    • 84865756636 scopus 로고    scopus 로고
    • DOI: 10.1002/chem.201201262
    • During revision of this manuscript, Enders et al. reported a chiral squaramide catalyzed asymmetric sulfenylation of N -Boc 3-substituted oxindoles. See: Wang, C.; Yang, X.; Loh, C. C. J.; Raabe, G.; Enders, D. Chem. - Eur. J. 2012, DOI: 10.1002/chem.201201262
    • (2012) Chem. - Eur. J.
    • Wang, C.1    Yang, X.2    Loh, C.C.J.3    Raabe, G.4    Enders, D.5
  • 77
    • 84866047082 scopus 로고    scopus 로고
    • CCDC 838460 contains the supplementary crystallographic data for 3k. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via
    • CCDC 838460 contains the supplementary crystallographic data for 3k. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www. ccdc.cam.ac.uk/data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.