在有机,制药,分析和环境用途中加速C2-H化
Shengkai Chen1, Jiannan Sun1, Hongmei Hu2
1College of Material, Chemistry and Chemical Engineering, Key Laboratory of Organosilicon Chemistry and Material Technology, Ministry of Education, Hangzhou Normal University, Hangzhou 311121, China.
Analytical chemistry
|June 12, 2025
概括
微滴化学有效地化弱极化合物,如异构和. 这种绿色化学方法为合成有价值的化化合物和药物提供了高效率.
科学领域:
- 有机化学 有机化学
- 绿色化学 绿色化学
- 分析化学 分析化学
背景情况:
- 微滴化学表现出独特的特性,如加速和极端的pH条件.
- 目前的应用主要集中在极性化合物上,对非极性或弱极性基板的研究有限.
研究的目的:
- 为了证明微滴化学对于涉及弱极化合物的反应的适用性.
- 使用微滴技术探索异构和的化.
主要方法:
- 使用微滴化学,用N-halosuccinimide来化和异.
- 开发了一种在线衍生策略,集成化和木合用于质谱.
主要成果:
- 成功合成了19种化 (异质) (3.22 g h-1 尺度).
- 制造了6种晚期化/化药物 (1.26 g h-1 尺度) 和5种单/多化碳醇.
- 在化反应中实现了高效率,温和条件和格拉姆可扩展性.
结论:
- 微滴化学非常适合化弱极化合物,扩大其合成效用.
- 这种方法提供了一种绿色,可持续和高效的途径,用于生产各种应用的化化合物.
相关概念视频
Halogenation of Alkenes
15.4K
Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence of inert and non-nucleophilic solvents, such as methylene chloride, chloroform, or carbon tetrachloride.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
15.4K
Electrophilic Addition to Alkynes: Hydrohalogenation
9.8K
Electrophilic addition of hydrogen halides, HX (X = Cl, Br or I) to alkenes forms alkyl halides as per Markovnikov's rule, where the hydrogen gets added to the less substituted carbon of the double bond. Hydrohalogenation of alkynes takes place in a similar manner, with the first addition of HX forming a vinyl halide and the second giving a geminal dihalide.
9.8K
Reactions at the Benzylic Position: Halogenation
2.4K
Benzylic halogenation takes place under conditions that favor radical reactions such as heat, light, or a free radical initiator like peroxide.
2.4K
Formation of Halohydrin from Alkenes
12.8K
An alkene, such as propene, reacts with bromine in the presence of water to yield a halohydrin. Halohydrins contain a halogen and a hydroxyl group attached to adjacent carbons. When the halogen is bromine, it is called a bromohydrin, while a chlorohydrin has chlorine as the halogen.
12.8K
Base-Promoted α-Halogenation of Aldehydes and Ketones
3.4K
α-Halogenation of aldehydes and ketones is a reaction involving the substitution of α hydrogens with halogens in the presence of a base. The reaction begins with the abstraction of α hydrogen by the base to produce a nucleophilic enolate ion. This intermediate undergoes a subsequent nucleophilic substitution with the halogen to produce a monohalogenated carbonyl compound. If the starting substrate has more than one α hydrogen, it is difficult to stop the reaction...
3.4K
Alkyl Halides
16.3K
Structural Properties
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
Alkyl halides are halogen-substituted alkanes wherein one or more hydrogen atoms of an alkane is replaced by a halogen atom such as fluorine, chlorine, bromine, or iodine. The carbon atom in an alkyl halide is bonded to the halogen atom, which is sp3-hybridized and exhibits a tetrahedral shape.
Unlike alkyl halides, compounds in which a halogen atom is bonded to an sp2 -hybridized carbon atom of a carbon-carbon double bond (C=C) are called vinyl halides. Whereas aryl...
16.3K


