绕过Mukaiyama氧化:通过硫胺-酒精合的选择性S-O键形成
Guoling Huang1, Huarui Zhu1, Shuting Zhou1
1School of Chemistry and Chemical Engineering, Lingnan Normal University, Zhanjiang, 524048, China.
Beilstein journal of organic chemistry
|January 28, 2026
概括
一种由NBS推广的新方法有效地从硫胺和酒精中合成硫胺酸. 这种无金属反应是可扩展的,对于制造性硫胺是有用的,这对于酶选择性合成是有价值的.
科学领域:
- 有机化学 有机化学
- 合成化学 合成化学
背景情况:
- 硫胺酸乙是一种有价值的合成中间体.
- 现有的合成方法通常需要恶劣的条件或缺乏选择性.
研究的目的:
- 开发一种新的,高效的,无金属的方法来合成硫胺酸.
- 为了探索这些的实用性在enantioselective合成.
主要方法:
- 硫胺与酒精的N-糖胺 (NBS) 促进的氧化合.
- 没有金属的反应条件.
- 可扩展到克的数量.
主要成果:
- 开发了一种选择性和高效的NBS促进的硫胺酸的合成.
- 证明了广泛的基质范围和高的化学选择性.
- 通过立体特异的格里格纳德替代物实现了硫胺的酶选择合成 (高达93% ee).
- 成功地将该方法应用于复杂酒精和生物活性分子的后期功能化.
结论:
- 苏尔菲尼米达酸是一种多功能中间体,可用于酶选择性S-C键的形成.
- 开发的协议为这些化合物提供了温和,无金属和高效的途径.
- 该方法适用于复杂的分子,并提供了对丰富硫胺的获取.
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