Related Experiment Video
Updated: Oct 7, 2025

Achieving Moderate Pressures in Sealed Vessels Using Dry Ice As a Solid CO2 Source
Published on: August 17, 2018
Enantioselective C-H Functionalization Reactions under Gold Catalysis.
1Department of Chemistry, Indian Institute of Science Education and Research Bhopal Bhauri, Bhopal, 462 066, India.
Gold catalysis enables enantioselective functionalization of C-H bonds, offering efficient synthesis of chiral molecules. This review highlights key advances in gold-catalyzed asymmetric C-H functionalization and its mechanistic underpinnings.
Area of Science:
- Organic Chemistry
- Catalysis
- Asymmetric Synthesis
Background:
- C-H bond functionalization is crucial for creating complex molecules efficiently.
- Gold catalysis offers unique reactivity for asymmetric transformations.
- Enantioselective synthesis is vital for pharmaceuticals and materials.
Purpose of the Study:
- To review recent advances in gold-catalyzed enantioselective C-H functionalization.
- To highlight the scope and limitations of these methodologies.
- To provide mechanistic insights into gold-catalyzed asymmetric reactions.
Main Methods:
- Literature review of enantioselective C-H functionalization reactions catalyzed by gold.
- Analysis of reaction mechanisms and catalyst performance.
- Discussion of key examples and synthetic strategies.
Main Results:
- Gold catalysts facilitate a variety of enantioselective C-H functionalization reactions.
- These methods provide access to valuable chiral building blocks.
- Mechanistic studies reveal the role of gold in controlling selectivity.
Conclusions:
- Gold catalysis is a powerful tool for asymmetric C-H functionalization.
- Continued development promises new synthetic routes to chiral compounds.
- Understanding mechanisms is key to designing improved catalytic systems.
More Related Videos
11:02Synthesis and Catalytic Performance of Gold Intercalated in the Walls of Mesoporous Silica
Published on: July 9, 2015
12:08Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
Published on: June 24, 2022
Related Concept Videos
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Regioselectivity of Electrophilic Additions-Peroxide Effect
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.
Preparation of 1° Amines: Hofmann and Curtius Rearrangement Mechanism
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn...
Limitations of Friedel–Crafts Reactions