Palladium‐Catalyzed Cascade Reaction for the Synthesis of Substituted Isoindolines

Abstract

Arylate then cyclize: A palladium(II)-catalyzed cascade sequence has been developed to provide highly diastereomerically enriched cis-1-aryl-3-vinyl isoindolines (see scheme). The method uses commercially available aryl boronic acids and boroxine compounds containing a variety of electron-rich, -neutral, or -poor aromatic groups. Ts=4-toluenesulfonyl. 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.