Affiliation:
1. Molecular Synthesis Center & Key Laboratory of Marine Drugs Ministry of Education; School of Medicine and Pharmacy Laboratory for Marine Drugs and Bioproducts of Marine Natural Products Ocean University of China 5 Yushan road Qingdao 266003 China
2. School of Chemistry and Chemical Engineering Key Laboratory of Colloid and Interface Chemistry Ministry of Education Shandong University 27 Shandanan road Jinan 250100 China
Abstract
AbstractTransition‐metal‐catalyzed [4+4] cycloaddition leading to cyclooctanoids has centered on dimerization between 1,3‐diene‐type substrates. Herein, we describe a [4σ+4π−1] and [4σ+4π] cycloaddition strategy to access 7/8‐membered fused carbocycles through rhodium‐catalyzed coupling between the 4σ‐donor (benzocyclobutenones) and pendant diene (4π) motifs. The two pathways can be controlled by adjusting the solvated CO concentration. A broad range (>40 examples) of 5–6–7 and 5–6–8 polyfused carbocycles was obtained in good yields (up to 90 %). DFT calculations, kinetic monitoring and 13C‐labeling experiments were carried out, suggesting a plausible mechanism. Notably, one 5–6–7 tricycle was found to be a very rare, potent, and selective ligand for the liver X receptor β (KD=0.64 μM), which is a potential therapeutic target for cholesterol‐metabolism‐related fatal diseases.