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Highly efficient synthesis of medium-sized lactones via oxidative lactonization: concise total synthesis of isolaurepan

机译:通过氧化内酯高效合成中等大小的内酯:简明全合成异烟酰胺

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摘要

A catalytic amount of TEMPO in the presence of PhI(OAc)_2 effected oxidative lactonization of 1,6- and 1,7-diols, directly affording seven- and eight-membered lactones, respectively, in good yields.rnLactone is a common structural motif widely found in biologically active natural products and Pharmaceuticals. In addition, a number of synthetic methods for functionalization of lactones are currently available, making them especially useful synthetic intermediates for the preparation of cyclic ethers. Thus, the development of practical synthetic methods for lactones continues to be an important and fundamental research in organic synthesis.
机译:在PhI(OAc)_2存在下催化量的TEMPO可以实现1,6-和1,7-二醇的氧化内酯化,分别直接以高收率提供七元和八元内酯.rn内酯是一种常见的结构广泛存在于生物活性天然产物和药物中的母题。另外,目前可获得许多用于内酯官能化的合成方法,这使它们成为用于制备环醚的特别有用的合成中间体。因此,开发实用的内酯合成方法仍然是有机合成的重要基础研究。

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  • 来源
    《Organic & biomolecular chemistry》 |2010年第1期|p.39-42|共4页
  • 作者单位

    Laboratory of Biostructural Chemistry, Graduate School of Life Sciences, Tohoku University, 1-1 Tsutsumidori-amamiya, Aoba-ku, Sendai 981-8555, Japan;

    Laboratory of Biostructural Chemistry, Graduate School of Life Sciences, Tohoku University, 1-1 Tsutsumidori-amamiya, Aoba-ku, Sendai 981-8555, Japan;

    Laboratory of Biostructural Chemistry, Graduate School of Life Sciences, Tohoku University, 1-1 Tsutsumidori-amamiya, Aoba-ku, Sendai 981-8555, Japan;

    Laboratory of Biostructural Chemistry, Graduate School of Life Sciences, Tohoku University, 1-1 Tsutsumidori-amamiya, Aoba-ku, Sendai 981-8555, Japan;

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