Molybdenum–Quinone-Catalyzed Deoxygenative Coupling of Aromatic Carbonyl Compounds

In the presence of triphenylphosphine as a mild reductant, the use of catalytic amounts of Mo­(CO)6 and an ortho-quinone ligand enables the intermolecular reductive coupling of aromatic aldehydes and the intramolecular coupling of aromatic ketones to produce functionalized alkenes. Diaryl- and diheteroaryl alkenes are synthesized with high (E)-selectivity and a tolerance toward bromide, iodide, and steric hindrance. Intramolecular coupling of dicarbonyl compounds under similar conditions affords mono- and disubstituted phenanthrenes

Additional file 1 of A feasibility study of provider-level implementation strategies to improve access to colorectal cancer screening for patients with schizophrenia: ACCESS2 (N-EQUITY 2104) trial

Additional file 1: Supporting file. A guide for encouraging cancer screening at psychiatric institutions