Iridium‐Catalyzed Asymmetric Allylic Aromatization Reaction

• Published in: Angewandte Chemie 2019-07, Vol.131 (31), p.10603-10609
• Main Authors: Liu, Xi‐Jia, Zheng, Chao, Yang, Yi‐Han, Jin, Shicheng, You, Shu‐Li
• Format: Article
• Language: English
• Subjects: Allylverbindungen; Aromatic compounds; Asymmetrische Katalyse; Chemical reactions; Chemistry; Equivalence; Heterocyclen; Heterocyclic compounds; Iridium; Nucleophiles; Substitution reactions; Synthesemethoden
• ISSN: 0044-8249; 1521-3757
• DOI: 10.1002/ange.201904156

Described herein is an asymmetric allylic aromatization (AAAr) strategy that employs readily accessible equivalents of benzylic nucleophiles in iridium‐catalyzed allylic substitution reactions with the concomitant formation of aromatic rings by aromatization. The optimized reaction conditions involving a catalyst derived from a commercially available iridium precursor and the Carreira ligand are compatible with equivalents of benzylic nucleophiles derived from 4‐ or 5‐methyloxazoles, 5‐methylthiazoles, 4‐ or 5‐methylfurans, 2‐ or 3‐methylbenzofurans, 3‐methylbenzothiophene, 3‐methylindole, 1‐methylnaphthalene, and methylbenzene. This strategy provides straightforward accesses to valuable heterocyclic aromatic compounds, bearing a homobenzylic stereogenic center, in an enantiopure form and would be difficult to access otherwise. The versatility of the reaction was showcased by the further elaboration of the products into useful building blocks and a drug analogue. Eine asymmetrische allylische Aromatisierung (AAAr) wird beschrieben, die leicht zugängliche benzylische Nukleophile in Iridium‐katalysierten allylischen Substitutionen mit gleichzeitiger Bildung aromatischer Ringe einsetzt. Diese Strategie ermöglicht den einfachen Zugang zu wertvollen Heteroarenen mit homobenzylischem stereogenem Zentrum in enantiomerenreiner Form.