催化剂/金属/无溶剂的马尔科夫尼科夫马尔科夫尼科夫马尔科夫尼科夫的未激活基因用二甲基酸的化
Azim Ziyaei Halimehjani1, Ziya Dağalan2, Zahra Marjani3
1Department of Chemistry, Sharif University of Technology, Tehran 11155-9516, Iran.
这项研究引入了一种新的无催化剂方法,用于使用dithiocarbamic酸的Markovnikov选择性化未激活. 这种方法有效地产生基二甲基碳酸盐,扩大了点击化学反应的范围.
科学领域:
- 有机化学 有机化学
- 合成化学 合成化学
背景情况:
- 马尔科夫尼科夫的选择性对未被激活的基化具有挑战性.
- 现有的方法通常需要催化剂,金属或特定的溶剂.
研究的目的:
- 开发一种无催化剂,无金属和无溶剂的方法,用于马尔科夫尼科夫的化.
- 从未激活的基中合成广泛的基二甲基碳酸盐.
主要方法:
- 在现场制备的dithiocarbamic酸.
- 三组分反应,涉及基和dithiocarbamic 酸.
- 使用未激活的终端,内部,循环和非循环基.
主要成果:
- 成功地通过马尔科夫尼科夫的选择性化方法,对各种未被激活的基进行了化.
- 有效合成多种类型的二甲基碳酸盐.
- 一个新的点击反应家族的演示.
结论:
- 已经建立了一个新的,高效的无催化剂协议,用于马尔科夫尼科夫的化.
- 这种方法为基二甲基碳酸盐提供了一条通用的途径.
- 这种反应代表了乙烯点击化学的重大进步.
更多相关视频
12:30Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
Published on: April 9, 2018
07:50Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
Published on: May 26, 2019
相关概念视频
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Radical Anti-Markovnikov Addition to Alkenes: Mechanism
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...
Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Radical Anti-Markovnikov Addition to Alkenes: Overview
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
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...
