Synthesis of sulfones via selective C-H-functionalization
Saad Shaaban1, Shuai Liang2, Nai-Wei Liu2
1Institute of Organic Chemistry and Chemical Biology, Goethe-University Frankfurt, Max-von-Laue-Str. 7, D-60438 Frankfurt am Main, Germany. g.manolikakes@chemie.uni-frankfurt.de and Organic Chemistry Division, Department of Chemistry, Faculty of Science, Mansoura University, El-Gomhorya Street, 35516 Mansoura, Egypt.
Direct C-H bond sulfonylation offers a powerful alternative for synthesizing sulfones. Recent advances showcase both metal-catalyzed and metal-free methods for C(sp2)-H and C(sp3)-H bond functionalization.
Area of Science:
- Organic Chemistry
- Synthetic Chemistry
Background:
- Sulfones are crucial compound classes in pharmaceuticals and materials science.
- Classical sulfone synthesis methods often require pre-functionalized substrates.
- Direct C-H bond functionalization offers a more atom-economical and efficient synthetic strategy.
Purpose of the Study:
- To review recent advancements in the direct sulfonylation of C-H bonds.
- To highlight both metal-catalyzed and metal-free methodologies.
- To cover transformations involving C(sp2)-H and C(sp3)-H bonds.
Main Methods:
- Review of literature on metal-catalyzed C-H sulfonylation.
- Analysis of metal-free C-H sulfonylation strategies.
- Focus on direct functionalization of aliphatic and aromatic C-H bonds.
Main Results:
- Significant progress in selective C-H sulfonylation over the past decade.
- Development of diverse catalytic systems for efficient sulfone synthesis.
- Emergence of metal-free protocols offering greener alternatives.
Conclusions:
- Direct C-H sulfonylation is a rapidly evolving and powerful synthetic approach.
- Both catalytic and non-catalytic methods provide versatile routes to sulfones.
- This strategy significantly streamlines the preparation of sulfone-containing molecules.
More Related Videos
12:30Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
Published on: April 9, 2018
05:34Efficient Synthesis of Polyfunctionalized Benzenes in Water via Persulfate-promoted Benzannulation of α,β-Unsaturated Compounds and Alkynes
Published on: December 16, 2019
Related Concept Videos
Preparation and Reactions of Sulfides
Electrophilic Aromatic Substitution: Sulfonation of Benzene
Preparation and Reactions of Thiols
Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions
Structure and Nomenclature of Thiols and Sulfides
Electrophilic Aromatic Substitution: Fluorination and Iodination of Benzene
