Eight-Step Asymmetric Synthesis of (–)-Berkelic Acid

Abstract

AbstractWe herein report an eight-step asymmetric synthesis of (–)-berkelic acid. This work features a sequential Catellani-type reaction/oxa-Michael addition with epoxides as dual-functionalized alkylating reagents for synthesizing the isochroman framework, a one-pot, acid-catalyzed deprotection/spiroacetalization process for the construction of a tetracyclic core intermediate, and a late-stage Ni-catalyzed reductive coupling reaction for the installation of the side chain. Remarkably, during the deprotection/spiroacetalization process, four new stereocenters are created with high stereocontrol from a single existing chiral center.