首页> 美国卫生研究院文献>Metabolites >Simultaneous Synthesis of Vitamins D2 D4 D5 D6 and D7 from Commercially Available Phytosterol β-Sitosterol and Identification of Each Vitamin D by HSQC NMR
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Simultaneous Synthesis of Vitamins D2 D4 D5 D6 and D7 from Commercially Available Phytosterol β-Sitosterol and Identification of Each Vitamin D by HSQC NMR

机译:从市售的植物甾醇β-谷甾醇同时合成维生素D2D4D5D6和D7并通过HSQC NMR鉴定每种维生素D

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摘要

We succeeded in simultaneously synthesizing the vitamin D family, vitamins D2, D4, D5, D6, and D7, from β-sitosterol, which is sold as a commercially available reagent from Tokyo Chemical Industry Co., Ltd. It is officially sold as a mixture of four phytosterols {β-sitosterol (40–45%), campesterol (20–30%), stigmasterol, and brassicasterol}. Owing to this, we anticipated that, using this reagent, various vitamin D analogs could be synthesized simultaneously. We also synthesized vitamin D3 from pure cholesterol and analyzed and compared all vitamin D analogs (D2, D3, D4, D5, D6, and D7) by HSQC NMR. We succeeded in clearly demonstrating the difference in the NMR chemical shifts for each vitamin D analog.
机译:我们成功地同时从β-谷甾醇合成了维生素D家族,维生素D2,D4,D5,D6和D7,后者是东京化学工业株式会社出售的市售试剂。四种植物甾醇的混合物{β-谷甾醇(40–45%),菜油甾醇(20–30%),豆甾醇和芸苔甾醇}。因此,我们预计使用该试剂可以同时合成各种维生素D类似物。我们还从纯胆固醇中合成了维生素D3,并通过HSQC NMR分析和比较了所有维生素D类似物(D2,D3,D4,D5,D6和D7)。我们成功地证明了每种维生素D类似物在NMR化学位移方面的差异。

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