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Enantioselective [2π + 2σ] Photocycloaddition Enabled by Brønsted Acid Catalyzed Chromophore Activation

Ellie F. Plachinski, Ruoyu Zoe Qian, Rodrigo Villanueva, Darren L. Poole, Tay Rosenthal, Tehshik P. Yoon

2024Journal of the American Chemical Society53 citationsDOIOpen Access PDF

Abstract

Bicyclo[2.1.1]hexanes have emerged as valuable scaffolds for the design of new pharmaceutical and agrochemical active ingredients. These structures can be efficiently synthesized via [2π + 2σ] photocycloadditions; however, control over the absolute stereochemistry of these strain-releasing reactions has remained challenging. Herein, we demonstrate that Brønsted acid catalyzed chromophore activation of C -acyl imidazoles enables highly enantioselective [2π + 2σ] photocycloadditions. Because this approach is agnostic to the identity of the coupling partner, the same strategy can be used to synthesize several other medicinally relevant strained small-ring structures.

Topics & Concepts

ChemistryEnantioselective synthesisChromophoreBrønsted–Lowry acid–base theoryCatalysisStereochemistryPhotochemistryOrganic chemistryRadical Photochemical ReactionsOxidative Organic Chemistry ReactionsCatalytic C–H Functionalization Methods
Enantioselective [2π + 2σ] Photocycloaddition Enabled by Brønsted Acid Catalyzed Chromophore Activation | Litcius