Kinetic Resolution of Tertiary Alcohols: Highly Enantioselective Access to 3‐Hydroxy‐3‐Substituted Oxindoles

Abstract

Enantioselektiv: Die erste hoch enantioselektive kinetische Racematspaltung von 3-Hydroxyoxindolen wurde mittels oxidativer Veresterung in Gegenwart eines N-heterocyclischen Carbens erreicht (siehe Bild). Die Methode liefert 3-substituierte Oxindole in hervorragender Eantiomerenreinheit. S=Selektivität 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.