Selective Synthesis of C4-Functionalized Benzofurans by Rhodium-Catalyzed Vinylene Transfer: Computational Study on the Cyclopentadienyl Ligand.
Junya KitanoYuji NishiiMasahiro MiuraPublished in: Organic letters (2022)
Benzofuran is a privileged structure in many bioactive compounds; however, the controlled synthesis of C2,C3-nonsubstituted benzofurans has been scarce. In particular, cumbersome multistep processes are inevitable for the most inaccessible C4-substituted isomers. Herein, we report a Rh-catalyzed direct vinylene annulation of readily available m -salicylic acid derivatives with vinylene carbonate to achieve selective construction of C4-substituted benzofurans. The Weinreb amide directing group facilitated the following product derivatization. The reaction mechanism was investigated by DFT calculations.
Keyphrases
- molecular docking
- density functional theory
- room temperature
- molecular dynamics simulations
- ms ms
- molecular dynamics
- quantum dots
- high performance liquid chromatography
- liquid chromatography
- gas chromatography mass spectrometry
- simultaneous determination
- tandem mass spectrometry
- atomic force microscopy
- molecularly imprinted
- monte carlo
- high resolution mass spectrometry