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Functional group translocation: moving functionalities without changing molecular scaffolds.
Eito Moriya1, Junichiro Yamaguchi1
1Department of Applied Chemistry, Waseda University, 513 Wasedatsurumakicho, Shinjuku, Tokyo 162-0041, Japan. junyamaguchi@waseda.jp.
Functional group translocation enables direct synthesis of positional isomers, crucial for drug discovery and materials science. This molecular editing strategy bypasses traditional inefficient routes, offering new possibilities in chemical synthesis.
Area of Science:
- Organic Chemistry
- Synthetic Chemistry
Background:
- Functional group position critically impacts molecular properties and biological activity.
- Synthesizing positional isomers traditionally requires inefficient, independent synthetic pathways.
- Positional isomers are vital for drug discovery and materials chemistry.
Purpose of the Study:
- To define and review functional group translocation reactions.
- To differentiate translocation from other isomerization processes.
- To highlight recent advances and future directions in the field.
Main Methods:
- Review of recent literature on functional group translocation.
- Categorization of reactions by molecular scaffold, functional group, and migration distance.
- Emphasis on transition metal catalysis and photoredox chemistry.
Main Results:
- Functional group translocation allows direct relocation of functional groups within a molecule.
- These reactions offer a concise strategy for accessing positional isomers from common precursors.
- Advances enable these transformations beyond classical stoichiometric methods.
Conclusions:
- Functional group translocation is a powerful synthetic tool for accessing positional isomers.
- This methodology streamlines synthesis for drug discovery and materials science.
- Further research can expand capabilities in synthesis and applications.

