阳离子类固醇-在- (III) 复杂启用非对称氧化N,N-二甲基硫胺胺
Yue Shen1, Xiao-Bao Wu1, Hua-Jie Jiang2
1Hefei National Research Center for Physical Sciences at the Microscale and Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, China.
Organic letters
|February 26, 2025
概括
阳离子 (III) 复合物催化N,N-二甲基硫胺的不对称氧化. 这种方法可以有效地产生具有高反选择性的奇拉三级硫胺,从而提供了一种新的合成途径.
科学领域:
- 有机金属化学 有机金属化学
- 不对称的催化剂.
- 硫化学 硫的化学
背景情况:
- N,N-二甲基硫胺是多功能合成前体.
- 开发对含硫化合物的酶选择性方法至关重要.
- 化三级硫胺是有机合成中有价值的构建模块.
研究的目的:
- 为N,N-二甲基硫胺开发一种新的非对称氧化方案.
- 作为催化剂,利用阳离子立体在 (III) 复合物.
- 为了获得具有高反选择性的多种奇拉三级硫胺.
主要方法:
- 不对称的氧化反应使用阳离子 () 复合物.
- 用各种N,N-二甲基硫胺基进行基质范围勘探.
- 异构分子比率 (e.r.) 的一个例子. 通过使用性染色学进行确定.
主要成果:
- 取得了N,N-二甲基硫胺的成功不对称氧化.
- 合成了多种多样的性三级硫胺 (24个例子).
- 获得了高选择性,最高可达94:6 e.r.
结论:
- 阳离子 (III) 复合物是不对称的硫胺氧化物的有效催化剂.
- 该协议提供了一种替代性和高效的途径,用于性硫胺.
- 有证据表明,在反应机制中存在一种性阴离子S(IV) 中间体.
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