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Volumn 65, Issue 43, 2009, Pages 8879-8884

Chiral imidates as a new class of nitrogen-based chiral ligands: synthesis and catalytic activity in asymmetric aziridinations and diethylzinc additions

Author keywords

Asymmetric aziridination; Asymmetric diethylzinc additions; Chiral imidates; Transition metal catalysis

Indexed keywords

AZIRIDINE DERIVATIVE; BENZALDEHYDE; CINNAMIC ACID; COPPER; COPPER COMPLEX; DIETHYLZINC; LIGAND; METAL; NITROGEN DERIVATIVE;

EID: 70349125414     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.08.028     Document Type: Article
Times cited : (24)

References (68)
  • 25
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    • The Chemistry of Functional Groups: The Chemistry of Amidines and Imidates, Patai S., Ed.; J. Wiley and Sons: London, New York, NY, 1975; 679 pp;
    • The Chemistry of Functional Groups: The Chemistry of Amidines and Imidates, Patai S., Ed.; J. Wiley and Sons: London, New York, NY, 1975; 679 pp;
  • 30
    • 70349159805 scopus 로고    scopus 로고
    • Imidates as pharmacophores
    • Imidates as pharmacophores:
  • 46
    • 70349099420 scopus 로고    scopus 로고
    • note
    • 3 at room temperature.
  • 51
    • 0042881024 scopus 로고    scopus 로고
    • For a review about enantioselective catalytic aziridinations:
    • For a review about enantioselective catalytic aziridinations:. Müller P., and Fruit C. Chem. Rev. 103 (2003) 2905-2919
    • (2003) Chem. Rev. , vol.103 , pp. 2905-2919
    • Müller, P.1    Fruit, C.2
  • 59
    • 0035263817 scopus 로고    scopus 로고
    • For a review about enantioselective dialkylzinc additions:
    • For a review about enantioselective dialkylzinc additions:. Pu L., and Yu H.-B. Chem. Rev. 101 (2001) 757-824
    • (2001) Chem. Rev. , vol.101 , pp. 757-824
    • Pu, L.1    Yu, H.-B.2
  • 63
    • 36148995872 scopus 로고    scopus 로고
    • For the synthesis of (1S,4S)-bicyclo[2.2.1]heptane-2,5-dione:
    • For the synthesis of (1S,4S)-bicyclo[2.2.1]heptane-2,5-dione:. Noël T., Vandyck K., and Van der Eycken J. Tetrahedron 63 (2007) 12961-12967
    • (2007) Tetrahedron , vol.63 , pp. 12961-12967
    • Noël, T.1    Vandyck, K.2    Van der Eycken, J.3
  • 66
    • 70349107077 scopus 로고    scopus 로고
    • note
    • The carbon signal was situated underneath the signals of DMSO. We could deduce the correct chemical shift from a coupling of the proton with the carbon in the HSQC spectrum.
  • 67
    • 70349148079 scopus 로고    scopus 로고
    • note
    • The synthesis of 2e is presented in the supporting information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.