首页> 外文期刊>The Journal of Organic Chemistry >Efficient conversion of cephalomannine to paclitaxel and 3'-N-Acyl-3'-N-debenzoylpaclitaxel analogs
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Efficient conversion of cephalomannine to paclitaxel and 3'-N-Acyl-3'-N-debenzoylpaclitaxel analogs

机译:高效将头孢甘氨酸转化为紫杉醇和3'-N-酰基-3'-N-去苯甲酰紫杉醇类似物

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摘要

The clinically important anticancer drug paclitaxel (Taxol) (1) was, until recently, available only by a complex and expensive isolation process from Taxus breuifolia bark, which is a nonrenewable and relatively scarce resource. This dependence on bark as the source of a drug required in ever increasing amounts focused both public and scientific interest on the discovery of alternate sources, and several approaches to the produc- tion of paclitaxel have been investigated.
机译:直到最近,临床上重要的抗癌药物紫杉醇(Taxol)(1)只能通过复杂且昂贵的从红豆杉树皮中分离得到,而紫杉树皮是不可再生且相对稀缺的资源。对树皮作为药物来源的依赖日益增加,这使得公众和科学兴趣都集中在发现替代来源上,并且已经研究了几种生产紫杉醇的方法。

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