相关实验视频
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Solid-phase Synthesis of [4.4] Spirocyclic Oximes
Published on: February 6, 2019
((III) 催化型选择性印度化以获得平面-状宏循环
Hongxuan Zhai1, Kang Lv2, Jiayan Li1
1Key Laboratory of Radiopharmaceuticals, Ministry of Education, College of Chemistry, Beijing Normal University, Beijing 100875, China.
这项研究引入了一种新的催化方法,用于用平面性-性合物合成复杂的宏循环. 这种新方法可以在单个步骤中高效地构建具有挑战性的全碳宏观循环结构.
科学领域:
- 有机化学
- 催化剂
- 合成方法
背景情况:
- 在具有生物活性的天然产品中,含有英多尔的宏循环很普遍.
- 通过宏循环化合成纯种,平面性-性醇仍然是一个重要的合成挑战.
研究的目的:
- 通过宏观循环制造开发第一个平面 - 合体的催化酶选择合成.
- 建立一种催化协议,用于涉及C-H激活和取消的选择性宏循环.
主要方法:
- (III) 催化素的C-H激活.
- 氧化 [3 + 2] 取消与分子内基.
- 形成平面 - 奇拉性内醇的非选择性宏循环.
主要成果:
- 一个新的单步协议用于内构造,宏循环化和平面性控制.
- 通过具有挑战性的全碳ANSA链,成功合成了宏环性体.
- 热力学研究表明,与氧-链相比,全碳链的旋转障碍较低.
结论:
- 开发的 (III) 催化方法提供了复杂的宏环性基体的有效途径.
- 计算研究阐明了该机制,强调了C-H激活和类插入作为反选择性的关键.
- 这项工作克服了宏循环平面 - 性的合成的一个主要障碍.
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