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Recent advances in Pd-catalyzed asymmetric cyclization reactions
Bing Xu1,2, Quanpu Wang1, Chao Fang1
1Department of Chemistry, Fudan University, 2005 Songhu Road, Shanghai, 200438, P. R. China. zhanmingzhang@fudan.edu.cn.
Recent progress in transition metal-catalyzed asymmetric cyclization reactions provides access to chiral molecules. Chiral palladium catalysts are key to these enantioselective transformations, driving innovation in synthesis.
Area of Science:
- Organic Chemistry
- Catalysis
- Asymmetric Synthesis
Background:
- Chiral carbo- and hetero-cycles are crucial building blocks in pharmaceuticals, agrochemicals, and materials.
- Transition metal-catalyzed asymmetric cyclization reactions offer efficient routes to these valuable structures.
- Chiral palladium catalysts exhibit remarkable efficacy in promoting enantioselective cyclization.
Purpose of the Study:
- To review the latest advancements in enantioselective palladium-catalyzed cyclization reactions.
- To cover developments over the past eleven years.
- To organize findings based on distinct transformation types.
Main Methods:
- Comprehensive literature survey of enantioselective palladium-catalyzed cyclization reactions.
- Categorization of reactions based on the specific transformations involved.
- Analysis of recent developments and key catalytic systems.
Main Results:
- Significant progress has been made in developing diverse chiral carbo- and hetero-cycles.
- Chiral palladium catalysis has proven highly effective for numerous enantioselective cyclizations.
- A wide array of transformations has been achieved with high enantioselectivity.
Conclusions:
- Enantioselective palladium-catalyzed cyclization reactions are powerful tools for synthesizing complex chiral molecules.
- The field has seen substantial innovation in the last eleven years.
- This review consolidates recent progress, highlighting the versatility and impact of palladium catalysis in asymmetric synthesis.
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