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 Introduction2 Classical Conditions for the Diels–Alder Cycloaddition2.1 Thermal Promotion2.2 High-Pressure Promotion2.3 Brønsted Acid Catalysis3 Modern Approaches to the Diels–Alder Cycloaddition3.1 Electron-Transfer Initiation3.2 Silver-Nanoparticle Catalysis3.3 Chiral-Boron-Complex Promotion4 Conclusion
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
