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Synthesis 2015; 47(11): 1519-1533
DOI: 10.1055/s-0034-1378696
DOI: 10.1055/s-0034-1378696
review
Recent Advances in the Total Synthesis of Prenylflavonoid and Related Diels–Alder Natural Products
Further Information
Publication History
Received: 27 January 2015
Accepted after revision: 02 March 2015
Publication Date:
13 April 2015 (online)
Abstract
This review summarizes the application of different strategies for the key Diels–Alder cycloaddition in prenylflavonoid and related Diels–Alder natural products synthesis, highlighting the application of novel methodologies and innovative strategies in the synthesis of these natural products and their analogues.
1 Introduction
2 Classical Conditions for the Diels–Alder Cycloaddition
2.1 Thermal Promotion
2.2 High-Pressure Promotion
2.3 Brønsted Acid Catalysis
3 Modern Approaches to the Diels–Alder Cycloaddition
3.1 Electron-Transfer Initiation
3.2 Silver-Nanoparticle Catalysis
3.3 Chiral-Boron-Complex Promotion
4 Conclusion
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For selected references on biological activities of Diels–Alder type natural products:
For recent hunts for the Diels–Alderase, see: