作者:Frederik Diness、Daniel S. Nielsen、David P. Fairlie
DOI:10.1021/jo201675r
日期:2011.12.2
fragment of the marine natural product largazole, a potent histone deacetylase 1 inhibitor, has been synthesized in five steps. The methodology provides rapid access to thiazole-4-carbonitrile, thiazole-4-carbimidate, thiazole–oxazoline, and other thiazole–thiazoline derivatives that are important intermediates in the total synthesis of many natural products with important biological properties.
海洋天然产物largazole(一种有效的组蛋白脱乙酰基酶1抑制剂)的噻唑-噻唑啉片段已通过五个步骤合成。该方法可以快速获得噻唑-4-腈,噻唑-4-氨基甲酸酯,噻唑-恶唑啉和其他噻唑-噻唑啉衍生物,它们是许多具有重要生物学特性的天然产物的总合成中的重要中间体。