Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

β-Dicarbonyl Compounds via Crossed Claisen Condensations01:18

β-Dicarbonyl Compounds via Crossed Claisen Condensations

3.1K
Crossed Claisen condensations are base-promoted reactions between two different ester molecules producing β-dicarbonyl compounds.  The reaction involving esters, with both containing α hydrogen, results in a mixture of four different products that are difficult to isolate. This reduces the synthetic utility of the reaction.
3.1K
Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview01:27

Vicinal Diols via Reductive Coupling of Aldehydes or Ketones: Pinacol Coupling Overview

1.8K
Wilhelm Rudolph Fittig discovered the pinacol coupling reaction in 1859. It is a radical dimerization reaction and involves the reductive coupling of aldehydes or ketones in the presence of hydrocarbon solvent to yield vicinal diols.
1.8K
Crossed Aldol Reactions: Overview01:04

Crossed Aldol Reactions: Overview

5.5K
Crossed aldol addition is the reaction between two different carbonyl compounds under acidic or basic conditions. Here, both the carbonyl compounds function as nucleophiles and electrophiles. As shown in Figure 1, such a reaction yields a mixture of products, two of which are formed via self-condensation, while the remaining two are formed via crossed-condensation. Without adjustment, the reaction's usefulness in organic chemistry is decreased.
5.5K
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation01:27

Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation

2.2K
Robinson annulation is a base-catalyzed reaction for the synthesis of 2-cyclohexenone derivatives from 1,3-dicarbonyl donors (such as cyclic diketones, β-ketoesters, or β-diketones) and α,β-unsaturated carbonyl acceptors. Named after Sir Robert Robinson, who discovered it, this reaction yields a six-membered ring with three new C–C bonds (two σ bonds and one π bond).
2.2K
Cycloaddition Reactions: MO Requirements for Thermal Activation01:16

Cycloaddition Reactions: MO Requirements for Thermal Activation

3.6K
Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.
3.6K
Cycloaddition Reactions: Overview01:16

Cycloaddition Reactions: Overview

2.6K
Cycloadditions are one of the most valuable and effective synthesis routes to form cyclic compounds. These are concerted pericyclic reactions between two unsaturated compounds resulting in a cyclic product with two new σ bonds formed at the expense of π bonds. The [4 + 2] cycloaddition, known as the Diels–Alder reaction, is the most common. The other example is a [2 + 2] cycloaddition.
2.6K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Modular enantioselective photocatalysts from privileged pybox scaffolds.

Science (New York, N.Y.)·2026
Same author

Oxygen migration into carbon-carbon single bonds by photochemical oxidation.

Nature synthesis·2026
Same author

Discovery of an ITK and TRK kinase inhibitor for the potential topical treatment of atopic dermatitis.

Nature communications·2026
Same author

Annulative Skeletal Diversification of Pyrimidines to Expanded Heteroaromatic Space.

Journal of the American Chemical Society·2025
Same author

Intermolecular transposed Paternò-Büchi reactions enabled by triplet sensitization.

Chemical science·2025
Same author

Direct C─H Lactonization of Carboxylic Acids Enabled by LMCT Photoactivation.

Angewandte Chemie (International ed. in English)·2025

相关实验视频

Updated: Jul 18, 2025

Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols
10:12

Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols

Published on: April 4, 2014

13.0K

铁介导的模块化脱碳化交叉核友合器.

Grace A Lutovsky1,2, Samuel N Gockel1,3, Mark W Bundesmann4

  • 1Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, WI 53706, USA.

Chem
|August 28, 2023
PubMed
概括
此摘要是机器生成的。

这项研究引入了一种使用铁盐和光化学直接合碳酸盐的新方法. 这种方法避免了昂贵的预功能化,并减少了化学合成中的有问题的副产品.

更多相关视频

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
11:44

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions

Published on: March 20, 2014

25.5K
A Two-Step Protocol for Umpolung Functionalization of Ketones Via Enolonium Species
08:12

A Two-Step Protocol for Umpolung Functionalization of Ketones Via Enolonium Species

Published on: August 16, 2018

10.0K

相关实验视频

Last Updated: Jul 18, 2025

Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols
10:12

Retropinacol/Cross-pinacol Coupling Reactions - A Catalytic Access to 1,2-Unsymmetrical Diols

Published on: April 4, 2014

13.0K
Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions
11:44

Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions

Published on: March 20, 2014

25.5K
A Two-Step Protocol for Umpolung Functionalization of Ketones Via Enolonium Species
08:12

A Two-Step Protocol for Umpolung Functionalization of Ketones Via Enolonium Species

Published on: August 16, 2018

10.0K

科学领域:

  • 有机化学 有机化学
  • 合成化学 合成化学
  • 摄影化学的使用.

背景情况:

  • 碳酸在制药发现中非常重要,因为它们的稳定性和多样性.
  • 目前的脱碳化合方法通常需要预功能化,增加成本和复杂性.
  • 现有的方法可以产生对环境的有机副产品.

研究的目的:

  • 开发一种直接脱碳化交叉合方法,用于原生碳素酸.
  • 使用廉价,丰富且无毒的铁 (III) 盐作为介质.
  • 为了实现多功能功能化,而无需预先功能化步骤.

主要方法:

  • 碳酸的光化学脱碳化.
  • 极端-极端交叉机制. 极端-极端交叉机制.
  • 使用Fe (III) 催化,与核友性伴侣进行交叉合.

主要成果:

  • 多种不同碳酸的成功直接脱碳化交叉合.
  • 碳-碳,碳-氧和碳-键的形成.
  • 证明Fe (III) 中介方法的普遍性和效率.

结论:

  • 开发的方法为碳酸功能化提供了一个可持续和高效的替代方案.
  • 这种方法简化了图书馆的合成,并减少了对环境的影响.
  • (III) 催化光化学为有机合成提供了一种多功能工具.