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Recent developments in decarboxylative C(aryl)-X bond formation from (hetero)aryl carboxylic acids
1Department of Chemistry, Indian Institute of Technology Delhi, Hauz Khas, New Delhi, 110016, India. ramuyadav@chemistry.iitd.ac.in.
Decarboxylative coupling reactions offer an efficient and greener method for creating new chemical bonds by releasing carbon dioxide. This review covers recent advances in forming carbon-heteroatom bonds using (hetero)aryl carboxylic acids.
Area of Science:
- Organic Chemistry
- Green Chemistry
Background:
- Decarboxylative coupling reactions provide efficient synthetic routes for C-C and C-X bond formation.
- Utilizing readily available (hetero)aryl carboxylic acids offers a sustainable alternative to traditional coupling methods.
- These reactions generate CO2 as the sole byproduct, aligning with green chemistry principles.
Purpose of the Study:
- To review recent advancements in ipso-decarboxylative C-X bond formations.
- To highlight the scope and limitations of using (hetero)aryl carboxylic acids in these coupling reactions.
- To identify future research directions in aryl-decarboxylative coupling.
Main Methods:
- Literature review of recent developments in decarboxylative coupling reactions.
- Focus on ipso-decarboxylative C-X (X = O/N/halo/S/Se/P/CN) bond formations.
- Analysis of reactions involving (hetero)aryl carboxylic acids.
Main Results:
- Summary of efficient C-C and C-X bond formations via decarboxylation.
- Demonstration of greener synthetic pathways with CO2 as a byproduct.
- Compilation of recent progress in ipso-decarboxylative coupling reactions.
Conclusions:
- Decarboxylative coupling reactions are a powerful tool for C-X bond formation.
- The use of (hetero)aryl carboxylic acids presents a sustainable and efficient approach.
- Further research is needed to overcome current limitations and expand the scope of these reactions.
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