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Volumn 13, Issue 6, 2011, Pages 1494-1497

Asymmetric aza-Mannich addition: Synthesis of modified chiral 2-(ethylthio)-thiazolone derivatives with anticancer potency

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; ANTINEOPLASTIC AGENT; CARBON; CINCHONA ALKALOID; THIAZOLE DERIVATIVE;

EID: 79952594088     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol200185h     Document Type: Article
Times cited : (40)

References (60)
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    • The United States Adopted Names (USAN) Council in The American Medical Association (AMA).
    • The United States Adopted Names (USAN) Council in The American Medical Association (AMA) (2005) Geometric Isomerism and Chirality: The USAN Perspective.
    • (2005) Geometric Isomerism and Chirality: The USAN Perspective
  • 47
    • 44349168328 scopus 로고    scopus 로고
    • For reviews on chiral cinchona alkaloid catalysts, see: Connon, S. J. Chem. Commun. 2008, 2499
    • (2008) Chem. Commun. , pp. 2499
    • Connon, S.J.1
  • 50
    • 0041378031 scopus 로고    scopus 로고
    • For selected examples of chiral cinchona alkaloid catalysis, see: J. Am. Chem. Soc. 2009, 131, 41
    • Chen, Y. G.; McDaid, P.; Deng, L. Chem. Rev. 2003, 103, 2965 For selected examples of chiral cinchona alkaloid catalysis, see: Liu, Y.; Sun, B. F.; Wang, B. M.; Wakem, M.; Deng, L. J. Am. Chem. Soc. 2009, 131, 41
    • (2003) Chem. Rev. , vol.103 , pp. 2965
    • Chen, Y.G.1    McDaid, P.2    Deng, L.3    Liu, Y.4    Sun, B.F.5    Wang, B.M.6    Wakem, M.7    Deng, L.8
  • 56
    • 0037436454 scopus 로고    scopus 로고
    • For chiral cinchona alkaloid catalysis in our group recently, see: Org. Lett. 2010, 12, 3914
    • Yoon, T. P.; Jacobsen, E. N. Science 2003, 299, 1691 For chiral cinchona alkaloid catalysis in our group recently, see: Sun, W. S.; Hong, L.; Liu, C. X.; Wang, R. Org. Lett. 2010, 12, 3914
    • (2003) Science , vol.299 , pp. 1691
    • Yoon, T.P.1    Jacobsen, E.N.2    Sun, W.S.3    Hong, L.4    Liu, C.X.5    Wang, R.6
  • 58
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    • Under the optimized conditions, the alkyl-substituted isobutyl N -tosyl imine showed no reactivity toward 2-(ethylthio)-thiazolone 2a.
    • Under the optimized conditions, the alkyl-substituted isobutyl N -tosyl imine showed no reactivity toward 2-(ethylthio)-thiazolone 2a.
  • 59
    • 79952586344 scopus 로고    scopus 로고
    • CCDC 800993 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
    • CCDC 800993 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/daa-request/cif.
  • 60
    • 79952615403 scopus 로고    scopus 로고
    • The dose-dependent growth inhibition ability was shown in the Supporting Information.
    • The dose-dependent growth inhibition ability was shown in the Supporting Information.


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