Palladium-Catalyzed Tandem Reaction of Yne-Propargylic Carbonates with Boronic Acids: A Simple Method for the Synthesis of Fused Aromatic Rings through Allene-Mediated Electrocyclization

The palladium‐catalyzed tandem reactions of yne–propargylic carbonates with aryl boronic acids, 2‐furyl boronic acid, and 2‐thiopheneboronic acid, followed by 6π‐electrocyclization to give fused ring aromatic products such as naphthalene, benzofuran, and benzothiophene derivatives are realized. Screening of the reaction conditions revealed that the combination of [Pd(PPh3)4] in THF gave the best results in terms of reactivity and product yields in the reaction of yne–propargylic carbonates with phenylboronic acid. The reaction is sensitive toward steric hindrance when substituted phenylboronic acids are emplyed. However, when we take 2‐furyl boronic acid as the organometallic reagent, most substrates perform very well to give benzofuran derivatives. In addition, 2‐thiopheneboronic acid is also a very effective coupling reagent to give bezothiophenes in high yields. A mechanism is proposed that involves the formation of an allenylpalladium complex from Pd0 and propargylic carbonate, followed by insertion of an intramolecular triple bond and the Suzuki coupling reaction, and then electrocyclization. Synthesis of fused ring compounds made easy: A series of fused ring compounds was easily prepared directly from palladium‐catalyzed coupling reactions of aryl boronic acids and linear yne–propargylic carbonates followed by electrocyclization (see scheme).