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CHEN Hao, YE Ji, LIU Jiangyun, ZHANG Weidong, SUN Qingyan. Total synthesis of the natural product of crinumaquine[J]. Journal of Pharmaceutical Practice and Service, 2015, 33(4): 331-333. doi: 10.3969/j.issn.1006-0111.2015.04.011
Citation: CHEN Hao, YE Ji, LIU Jiangyun, ZHANG Weidong, SUN Qingyan. Total synthesis of the natural product of crinumaquine[J]. Journal of Pharmaceutical Practice and Service, 2015, 33(4): 331-333. doi: 10.3969/j.issn.1006-0111.2015.04.011

Total synthesis of the natural product of crinumaquine

doi: 10.3969/j.issn.1006-0111.2015.04.011
  • Received Date: 2014-05-30
  • Rev Recd Date: 2014-09-09
  • Objective To complete the synthesis of the natural product of crinumaquine. Methods 3,4-methylenedioxyphenethylamine and 2,5-dimthoxyphenylacetic were taken as starting material, and chemical reactions of condensation, cyclization, reduction, oxidation and other reactions were conducted. Results and Conclusion The optimum synthetic route was determinedunder which the final yield rate was 73%.
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Total synthesis of the natural product of crinumaquine

doi: 10.3969/j.issn.1006-0111.2015.04.011

Abstract: Objective To complete the synthesis of the natural product of crinumaquine. Methods 3,4-methylenedioxyphenethylamine and 2,5-dimthoxyphenylacetic were taken as starting material, and chemical reactions of condensation, cyclization, reduction, oxidation and other reactions were conducted. Results and Conclusion The optimum synthetic route was determinedunder which the final yield rate was 73%.

CHEN Hao, YE Ji, LIU Jiangyun, ZHANG Weidong, SUN Qingyan. Total synthesis of the natural product of crinumaquine[J]. Journal of Pharmaceutical Practice and Service, 2015, 33(4): 331-333. doi: 10.3969/j.issn.1006-0111.2015.04.011
Citation: CHEN Hao, YE Ji, LIU Jiangyun, ZHANG Weidong, SUN Qingyan. Total synthesis of the natural product of crinumaquine[J]. Journal of Pharmaceutical Practice and Service, 2015, 33(4): 331-333. doi: 10.3969/j.issn.1006-0111.2015.04.011
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