Chemoselective and Regioselective Synthesis of Spiroisoindolinone Indenes via an Intercepted Meyer–Schuster Rearrangement/Intramolecular Friedel–Crafts Alkylation Relay
Nikola Topolovčan, Marina Degač, Ana Čikoš, Matija Gredičak
Abstract
A Brønsted acid-catalyzed reaction between isoindolinone-derived propargylic alcohols and external aromatic nucleophiles for the construction of spiroisoindolinone indenes is described. The reaction proceeds rapidly with a broad range of substrates to generate spiroindenes chemoselectively and regioselectively in moderate to high yields. Key to the success of this transformation is an intercepted Meyer-Schuster rearrangement/intramolecular Friedel-Crafts alkylation relay that offers a modular approach in the synthesis of target compounds.
Topics & Concepts
ChemistryRegioselectivityIntramolecular forceFriedel–Crafts reactionAlkylationCope rearrangementNucleophileCombinatorial chemistryStereochemistryOrganic chemistryCatalysisSynthetic Organic Chemistry MethodsSynthesis and pharmacology of benzodiazepine derivativesOxidative Organic Chemistry Reactions