期刊
JOURNAL OF COMBINATORIAL CHEMISTRY
卷 8, 期 2, 页码 268-274出版社
AMER CHEMICAL SOC
DOI: 10.1021/cc050143n
关键词
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The generation of a natural-product-based library starting from andrographolide is described. Utilizing andrographolide itself in parallel solution-phase synthesis leads to a 360-membered library. The initial transformation of the starting material via ozonolysis is followed by the conversion into a suitable template by introduction of a thiazole moiety. Subsequent decoration at two points of diversity yields the desired natural product derivatives. The selection of actually synthesized compounds is based on a virtually generated library and the assessment of its members with respect to physicochemical parameters, thus ensuring pharmacological relevance of the compounds.
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