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Volumn , Issue 14, 2005, Pages 1898-1900

Second-generation organocatalysts for the highly enantioselective dynamic kinetic resolution of azlactones

Author keywords

[No Author keywords available]

Indexed keywords

AZLACTONE DERIVATIVE; LACTONE DERIVATIVE; TERTIARY AMINE; THIOUREA DERIVATIVE; UNCLASSIFIED DRUG;

EID: 17444385209     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b418666d     Document Type: Article
Times cited : (148)

References (21)
  • 10
    • 17444380177 scopus 로고    scopus 로고
    • A. Berkessel, F. Cleemann, S. Mukherjee, T. N. Müller and J. Lex, Angew. Chem., 2005, 117, 817; A. Berkessel, F. Cleemann, S. Mukherjee, T. N. Müller and J. Lex, Angew. Chem. Int. Ed., 2005, 44, 807. Catalysts of the thiourea-tert-amine type were applied before by Takemoto et al. for asymmetric aza-Henry reactions and Michael additions: T. Okino, S. Nakamura, T. Furukawa and Y. Takemoto, Org. Lett., 2004, 6, 625; T. Okino, Y. Hoashi and Y. Takemoto, J. Am. Chem. Soc., 2003, 125, 12672.
    • (2005) Angew. Chem. , vol.117 , pp. 817
    • Berkessel, A.1    Cleemann, F.2    Mukherjee, S.3    Müller, T.N.4    Lex, J.5
  • 11
    • 13444270903 scopus 로고    scopus 로고
    • A. Berkessel, F. Cleemann, S. Mukherjee, T. N. Müller and J. Lex, Angew. Chem., 2005, 117, 817; A. Berkessel, F. Cleemann, S. Mukherjee, T. N. Müller and J. Lex, Angew. Chem. Int. Ed., 2005, 44, 807. Catalysts of the thiourea-tert-amine type were applied before by Takemoto et al. for asymmetric aza-Henry reactions and Michael additions: T. Okino, S. Nakamura, T. Furukawa and Y. Takemoto, Org. Lett., 2004, 6, 625; T. Okino, Y. Hoashi and Y. Takemoto, J. Am. Chem. Soc., 2003, 125, 12672.
    • (2005) Angew. Chem. Int. Ed. , vol.44 , pp. 807
    • Berkessel, A.1    Cleemann, F.2    Mukherjee, S.3    Müller, T.N.4    Lex, J.5
  • 12
    • 1342268984 scopus 로고    scopus 로고
    • A. Berkessel, F. Cleemann, S. Mukherjee, T. N. Müller and J. Lex, Angew. Chem., 2005, 117, 817; A. Berkessel, F. Cleemann, S. Mukherjee, T. N. Müller and J. Lex, Angew. Chem. Int. Ed., 2005, 44, 807. Catalysts of the thiourea-tert-amine type were applied before by Takemoto et al. for asymmetric aza-Henry reactions and Michael additions: T. Okino, S. Nakamura, T. Furukawa and Y. Takemoto, Org. Lett., 2004, 6, 625; T. Okino, Y. Hoashi and Y. Takemoto, J. Am. Chem. Soc., 2003, 125, 12672.
    • (2004) Org. Lett. , vol.6 , pp. 625
    • Okino, T.1    Nakamura, S.2    Furukawa, T.3    Takemoto, Y.4
  • 13
    • 0142072631 scopus 로고    scopus 로고
    • A. Berkessel, F. Cleemann, S. Mukherjee, T. N. Müller and J. Lex, Angew. Chem., 2005, 117, 817; A. Berkessel, F. Cleemann, S. Mukherjee, T. N. Müller and J. Lex, Angew. Chem. Int. Ed., 2005, 44, 807. Catalysts of the thiourea-tert-amine type were applied before by Takemoto et al. for asymmetric aza-Henry reactions and Michael additions: T. Okino, S. Nakamura, T. Furukawa and Y. Takemoto, Org. Lett., 2004, 6, 625; T. Okino, Y. Hoashi and Y. Takemoto, J. Am. Chem. Soc., 2003, 125, 12672.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 12672
    • Okino, T.1    Hoashi, Y.2    Takemoto, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.