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Synthetic studies in the quassinoid series. Conversion of chaparrin into castelanone and quassinoid analogs.
Tetrahedron Letters ( IF 1.5 ) Pub Date : 1982 , DOI: 10.1016/s0040-4039(00)87397-9
Andrew J. Caruso , Judith Poplonsky , Bertha Soto Rodriguez

Inactive chaparrin has been converted in seven steps and in 16% overall yield to castelanone which is known to inhibit significantly growth of the murine lymphocytic leukemia P-388 cell line. The methodology developed has been applied to the preparation of quassinoid analogs , and .

中文翻译:

拟似系列的综合研究。查帕林将其转化为二十烷酮和类茜素类似物。

失活的查帕林经过七个步骤,以总收率的16%转化为Castelanone ,众所周知,Caselanone可以显着抑制鼠淋巴细胞性白血病P-388细胞系的生长。开发的方法已应用于拟拟南芥类似物
更新日期:2017-01-31
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