Rapid Assembly of Resorcylic Acid Lactone Frameworks through Sequential Palladium‐Catalyzed Coupling Reactions

Abstract

Just three steps! The highly efficient synthesis of 15 analogues of resorcylic acid lactones has been achieved through sequential palladium-catalyzed coupling reactions based on the aromatic scaffolds and ring-closing metathesis reactions. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.