Synthesis of Hexahydroindoles by Intramolecular CH Alkenylation: Application to the Synthesis of the Core of Aeruginosins

Abstract

Vorstoß zum Kern: Pd-katalysierte intramolekulare C-H-Arylierungen wurden auf Alkenylierungen ausgeweitet. Die Methode ist bemerkenswert selektiv und liefert nützliche Hexahydroindole, wie durch die Synthese des Octahydroindolkerns der Aeruginosin-Naturstofffamilie veranschaulicht wurde (siehe Schema). 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.