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Volumn 38, Issue 35, 1997, Pages 6173-6176

Copper(I) catalyzed conjugate addition of Grignard reagents to acrylic acids: Homologation of artemisinic acid and subsequent conversion to 9-substituted artemisinin analogs

Author keywords

[No Author keywords available]

Indexed keywords

ARTEMISIN DERIVATIVE; ARTEMISINIC ACID; COPPER; DIHYDROARTEMISININ; REAGENT;

EID: 0030839737     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)01428-7     Document Type: Article
Times cited : (23)

References (31)
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    • Jung, M. Curr. Med. Chem. 1994, 1, 35-49. Meshnick, S. R.; Taylor, T. E. and Kamchonwongpaisan, S. Microbiol. Rev. 1996, 60, 301-315. Cumming, J. N.; Ploypradith, P. and Posner, G. H. Adv. Pharmacol. 1997, 56, 7-12.
    • (1996) Microbiol. Rev. , vol.60 , pp. 301-315
    • Meshnick, S.R.1    Taylor, T.E.2    Kamchonwongpaisan, S.3
  • 7
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    • Jung, M. Curr. Med. Chem. 1994, 1, 35-49. Meshnick, S. R.; Taylor, T. E. and Kamchonwongpaisan, S. Microbiol. Rev. 1996, 60, 301-315. Cumming, J. N.; Ploypradith, P. and Posner, G. H. Adv. Pharmacol. 1997, 56, 7-12.
    • (1997) Adv. Pharmacol. , vol.56 , pp. 7-12
    • Cumming, J.N.1    Ploypradith, P.2    Posner, G.H.3
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    • note
    • 28 Known quantities from each run of dried, crude reaction product were then analyzed by HPLC and the yield and isomer ratios were quantitated relative to controls. In two examples, isolated yields (silica gel flash chromatography, 20% EtOAc/hexane) were determined in order to validate the HPLC method (Table 1). All compounds displayed satisfactory spectral and analytical data.


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