Related Experiment Video
Updated: Jul 6, 2026

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs)
Published on: January 17, 2020
Carboxylic acids as substrates in homogeneous catalysis.
Lukas J Goossen1, Nuria Rodríguez, Käthe Goossen
1FB Chemie-Organische Chemie, TU Kaiserslautern, Erwin-Schrödinger-Strasse Geb. 54, 67663 Kaiserslautern, Germany. goossen@chemie.uni-kl.de
Carboxylic acids are versatile organic building blocks. New catalytic methods enable their direct use in synthesis, expanding accessible product classes without prior activation, simplifying organic reactions.
Area of Science:
- Organic Chemistry
- Catalysis
- Synthetic Methodology
Background:
- Carboxylic acid groups are common in organic molecules.
- Activated derivatives are traditionally used for derivatization and carbon framework construction.
- Recent advances enable direct use of carboxylic acids without activation.
Purpose of the Study:
- To review catalytic transformations of carboxylic acids.
- To highlight derivatives accessible in situ.
- To encourage further development and application of these methods.
Main Methods:
- Catalytic transformations of carboxylic acids.
- In situ generation of derivatives.
- Organometallic catalysis involving acyl and carboxylate complexes.
Main Results:
- Carboxylic acids can serve as synthetic equivalents for acyl, aryl, or alkyl halides and organometallic reagents.
- Catalytic cycles can release carbon monoxide or carbon dioxide, forming diverse organometallic species.
- A wide range of product classes are accessible from carboxylic acids.
Conclusions:
- Catalytic methods significantly enhance the utility of carboxylic acids in organic synthesis.
- These transformations offer multifaceted reaction pathways.
- The review invites further research and application of these novel synthetic strategies.
Related Concept Videos
Reactions of Carboxylic Acids: Introduction
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...
Heterogeneous Catalysis
Preparation of Carboxylic Acids: Overview
Preparation of Carboxylic Acids: Hydrolysis of Nitriles

