Expeditious Synthesis of Tetrasubstituted Helical Alkenes by a Cascade of Palladium‐Catalyzed CH Activations

Nach einem modularen Ansatz wurden tetrasubstituierte helicale Alkene hergestellt. Dabei ermöglicht eine intermolekulare, Pd-katalysierte und Norbornen-vermittelte Dominoreaktion die Bildung dreier C-C-Bindungen in einem einzigen Arbeitsschritt über eine Sequenz aus C-H-Aktivierung, Carbopalladierung und erneuter C-H-Aktivierung. 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.