被催化物捕获的基:马尔科夫尼科夫的-反应的方法
Rong-Jin Zhang1, Xiang-Rui Li1, Rong-Bin Liang1
1College of Chemistry and Chemical Engineering, and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, Shantou 515063, P. R. China.
Organic letters
|January 12, 2024
概括
这项研究介绍了一种新的催化马尔科夫尼科夫醇-反应,使用基,克服典型的反马尔科夫尼科夫选择性. 这种高效的协议为复杂分子合成提供了广泛的范围和可扩展性.
科学领域:
- 有机化学 有机化学
- 催化剂是一种催化剂.
- 激进的反应 激进的反应
背景情况:
- 硫醇-乙烯反应是有机合成中的通用工具.
- 由于固有的反马尔科夫尼科夫偏好,在激进的乙烯反应中实现马尔科夫尼科夫的选择性是具有挑战性的.
- 现有的方法通常需要特定的氧化剂或缺乏区域选择性.
研究的目的:
- 举报一个罕见的马尔科夫尼科夫的乙烯反应的例子,由基介导.
- 开发一种催化协议,实现独特的马尔科夫尼科夫地区选择性.
- 证明开发方法的广泛适用性和可扩展性.
主要方法:
- 使用催化剂来控制烯反应的区域选择性.
- 在催化条件下使用基中间体.
- 探索各种各样的基质,以确定反应范围.
主要成果:
- 成功开发了一种新的催化马尔科夫尼科夫乙烯反应.
- 该协议只能产生马尔科夫尼科夫的加法产品,克服固有的激进路径偏差.
- 反应表明了广泛的基质范围,避免了需要专门的氧化剂.
结论:
- 这项工作为马尔科夫尼科夫的烯反应建立了一个实用和区域选择性的方法.
- 催化方法为通过后期修改合成复杂分子提供了有价值的工具.
- 该协议的可扩展性和效率突显了其合成效用.
相关概念视频
Radical Reactivity: Nucleophilic Radicals
2.1K
Radicals adjacent to electron-donating groups are called nucleophilic radicals. These radicals readily react with electrophilic alkenes. The SOMO–LUMO interactions are the driving force for the reaction, where the high-energy SOMO of the electron-rich, nucleophilic radicals interacts with the low-energy LUMO of the electron-deficient, electrophilic alkenes. Such SOMO–LUMO interactions are the basis of reactive radical traps, affecting the selectivity in radical reactions. For...
2.1K
Radical Anti-Markovnikov Addition to Alkenes: Mechanism
3.8K
The reaction of hydrogen bromide with alkenes in the presence of hydroperoxides or peroxides proceeds via anti-Markovnikov addition. The radical chain reaction comprises initiation, propagation, and termination steps.
The mechanism starts with chain initiation, which involves two steps. In the first chain initiation step, a weak peroxide bond is homolytically cleaved upon mild heating to form two alkoxy radicals. In the second initiation step, a hydrogen atom is abstracted by the alkoxy...
The mechanism starts with chain initiation, which involves two steps. In the first chain initiation step, a weak peroxide bond is homolytically cleaved upon mild heating to form two alkoxy radicals. In the second initiation step, a hydrogen atom is abstracted by the alkoxy...
3.8K
Radical Anti-Markovnikov Addition to Alkenes: Overview
3.4K
The addition of hydrogen bromide to alkenes in the presence of hydroperoxides or peroxides proceeds via an anti-Markovnikov pathway and yields alkyl bromides.
3.4K
Preparation and Reactions of Thiols
6.2K
Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol.
6.2K
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
1.8K
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation...
1.8K
Radical Reactivity: Intramolecular vs Intermolecular
1.7K
Radical reactions can occur either intermolecularly or intramolecularly. In an intermolecular radical reaction, a nucleophilic radical adds to an electrophilic alkene or vice versa. In such reactions, the radical and generally the alkene, which is also called the radical trap, are two different molecules. Additionally, for such intermolecular reactions to occur, the radical trap must be active, present in an excess concentration, and the radical starting material must have a weak...
1.7K


