Chiral Hypervalent Iodines: Active Players in Asymmetric Synthesis
1Facultad de Ciencias, Departamento de Química Orgánica, Institute for Advance Research in Chemical Sciences (IAdChem) Universidad Autónoma de Madrid , 28049 Madrid , Spain.
Chiral hypervalent iodine reagents enable efficient asymmetric organocatalytic oxidations. This review covers their preparation and diverse reactivity in enantioselective synthesis.
Area of Science:
- Organic Chemistry
- Asymmetric Synthesis
- Catalysis
Background:
- Chiral hypervalent iodine reagents have significantly advanced asymmetric organocatalytic oxidations.
- These reagents offer advantages such as ease of handling, low toxicity, mild reaction conditions, and environmental friendliness.
Purpose of the Study:
- To provide a comprehensive overview of methods for preparing chiral iodine(III/V) compounds.
- To highlight the reactivity of these reagents in various enantioselective transformations.
Main Methods:
- Review of literature on the synthesis of chiral hypervalent iodine reagents.
- Analysis of reported catalytic and stoichiometric applications in asymmetric synthesis.
Main Results:
- Numerous approaches for synthesizing chiral iodine(III/V) species have been developed.
- These reagents facilitate a wide range of unprecedented enantioselective transformations.
Conclusions:
- Chiral hypervalent iodine(III/V) reagents are versatile tools in asymmetric organocatalysis.
- Their unique properties and reactivity continue to drive innovation in enantioselective synthesis.
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