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An improved synthesis of 3β-cholesteryl halides involving i-steroid and retro-i-steroid rearrangements

机译:改善合成3β-胆甾醇卤化物,涉及I-甾体醇和retro-I类固醇重排

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摘要

Treatment of 3β-cholesteryl methanesulfonate with tetrabutylammonium halides in the presence of BF_3·Et_2O provides a mild and efficient method for the preparation of 3β-cholesteryl halides via i-steroid and retro-i-steroid rearrangements. The utilization of tetrabutylammonium halides avoided the moisture sensitivity and lowered the cost of reagents for the reported method based on trimethylsilyl halides.
机译:在BF_3·ET_2O存在下将3β-胆甾醇甲磺酸盐用四丁基卤化物提供了一种温和,有效的方法,用于制备3β-Cholesteryl卤化物,通过I类动物和Retro-I类固醇重排。卤化丁基铵的利用避免了水分敏感性,并降低了基于三甲基甲硅烷基卤化物的报告方法的试剂的成本。

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