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相关概念视频

Oxidation of Phenols to Quinones01:17

Oxidation of Phenols to Quinones

4.4K
In the presence of oxidizing agents, phenols are oxidized to quinones. Quinones can be easily reduced back to phenols using mild reducing agents. The electron-donating hydroxyl group enhances the reactivity of the aromatic ring, enabling oxidation of the ring even in the absence of an α hydrogen.
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
4.4K
Electron Transport Chain: Complex III and IV01:43

Electron Transport Chain: Complex III and IV

8.9K
During the electron transport chain, electrons from NADH and FADH2 are first transferred to complexes I and II, respectively. These two complexes then transfer the electrons to ubiquinol, which carries them further to complex III. Complex III passes the electrons across the intermembrane space to Cyt c, which carries them further to complex IV. Complex IV donates electrons to oxygen and reduces it to water. As electrons pass through complexes I, III, and IV, the energy released aids the pumping...
8.9K
The Electron Transport Chain01:30

The Electron Transport Chain

19.4K
The electron transport chain or oxidative phosphorylation is an exothermic process in which free energy released during electron transfer reactions is coupled to ATP synthesis. This process is a significant source of energy in aerobic cells, and therefore inhibitors of the electron transport chain can be detrimental to the cell's metabolic processes.
Inhibitors of the electron transport chain
Rotenone, a widely used pesticide, prevents electron transfer from Fe-S cluster to ubiquinone or Q...
19.4K
Electron Transport Chain: Complex I and II01:46

Electron Transport Chain: Complex I and II

18.3K
The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
18.3K
Electron Transport Chains01:28

Electron Transport Chains

111.1K
The final stage of cellular respiration is oxidative phosphorylation that consists of two steps: the electron transport chain and chemiosmosis. The electron transport chain is a set of proteins found in the inner mitochondrial membrane in eukaryotic cells. Its primary function is to establish a proton gradient that can be used during chemiosmosis to produce ATP and generate electron carriers, such as NAD+ and FAD, that are used in glycolysis and the citric acid cycle.
The ETC is comprised of...
111.1K
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

3.1K
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
3.1K

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Facile Preparation of 4-Substituted Quinazoline Derivatives
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Facile Preparation of 4-Substituted Quinazoline Derivatives

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化学酶的甲基形成

Tyler J Doyon, Jonathan C Perkins, Summer A Baker Dockrey

    Journal of the American Chemical Society
    |December 17, 2019
    PubMed
    概括

    使用特定的铁酶进行生物催化,在温和的条件下产生反应性o甲基中间体. 这使得选择性C-H键功能化在复杂分子合成的化学酶级联中.

    科学领域:

    • 有机化学
    • 生物催化
    • 合成化学

    背景情况:

    • 大自然利用反应性中间体来实现分子复杂性.
    • 在温和条件下选择性生成反应性物种仍然是一个合成挑战.

    研究的目的:

    • 证明生物催化剂产生具有高化学选择性的o甲基中间体.
    • 开发一种温和的水性方法来实现C-H键的功能化.

    主要方法:

    • 使用了依赖α-甲酸的非血铁酶 (CitB和Clad).
    • 在o-cresol基质中使用基C-H键的生物催化化.
    • 在单化酶级联中促进核/二基因的拦截.

    主要成果:

    • 在温和的水性条件下实现基C-H键的选择性修饰.
    • 证明了C-H债券转换为C-C,C-N,C-O和C-S债券的一次性转换.
    • 展示了选择性改和合成的天然产品 (-) - xyloketal D.

    结论:

    • 生物催化提供了一个强大的平台来产生具有精确化学选择性的反应性中间体.
    • 这种化学酶方法能够有效和温和地发挥C-H键的作用.

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  • 该方法适用于复杂分子合成,包括天然产品和.