Copper‐Catalyzed Arylative Meyer–Schuster Rearrangement of Propargylic Alcohols to Complex Enones Using Diaryliodonium Salts

Abstract

Kupplung nach Belieben: Eine Kupfer-katalysierte arylierende Meyer-Schuster-Umlagerung wird beschrieben, die mit einer Bandbreite von substituierten Propargylalkoholen und Diaryliodoniumsalzen kompatibel ist. Die Reaktion liefert komplexe trisubstituierte Enone selektiv als E-Isomere. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to 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.