在Rh-催化下对基的副化
David E Olson1, Justin Y Su, D Allen Roberts
1Department of Chemistry, Stanford University , Stanford, California 94305-5080, United States.
一种新的双重反应产生了从亚齐里迪纳和重新排列中受保护的二胺. 这种高效的方法可以合成有价值的邻近二胺,包括在enduracididine中发现的二胺.
科学领域:
- 有机化学 有机化学
- 合成化学 合成化学
背景情况:
- 1,2-二胺是有机合成中至关重要的构建块.
- 现有的合成1,2-二胺的方法可能是漫长的或需要恶劣的条件.
研究的目的:
- 开发一种新,高效的单步方法,用于合成差异保护的邻近二胺.
- 为了证明这种新方法在合成复杂的自然产品中的实用性.
主要方法:
- 一个串联序列,涉及Rh催化阿齐里迪纳,其次是NaI促进的重排.
- 在热水和中循环硫胺中间体的环开口.
主要成果:
- 通过一步联动过程成功合成1,2-二胺.
- 通过简易的环开口产生差异保护的邻近二胺.
- 使用该方法合成 (±) - 内酸和 (±) - - 内酸.
结论:
- 开发的双重反应提供了一条有效的途径,以获得有价值的1,2-胺衍生物.
- 这种方法提供了一个通用的平台,可以访问复杂的分子,包括天然产品.
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