【摘 要】
：
A series of novel azasterols 8a―8h and 10a―10c were synthesized from the key intermediate 6 by acylation and deprotection. Compound 6 was obtained through a s
【机 构】
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School of Chemical Engineering and Technology,College of Science
【基金项目】
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Supported by the National Natural Science Foundation of China
论文部分内容阅读
A series of novel azasterols 8a―8h and 10a―10c were synthesized from the key intermediate 6 by acylation and deprotection. Compound 6 was obtained through a series of reactions including Wittig reaction, etherification, ene reaction, oxidation, oximation and reduction. Structures of the synthesized compounds were confirmed by IR, MS and 1H NMR. Furthermore, all of these compounds were screened for in vitro antiparasitic activity against L. donovani. Among them, compounds 8h, 10a and 10b showed a fair inhibition of leishmania promastigotes growth at 25 μg/mL, with potencies close to that of the reference drug, amphotericin B. The results provide a starting point for the development of novel drugs to treat leishmaniasis.
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