Abstract
A one-pot procedure involving a four-component Ugi reaction followed by an intramolecular Diels–Alder reaction/HCl elimination cascade has been developed to provide rapid access to the isoindolinone framework in a diversity-oriented fashion. The scope of the process has been investigated with respect to all four components, and a comparison between the one-pot and sequential approaches is given. The possibility of a late-stage one-pot functionalization through Suzuki coupling has been explored.
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Huang, J., Du, X., Van Hecke, K., Van der Eycken, E. V., Pereshivko, O. P., & Peshkov, V. A. (2017). Ugi Reaction Followed by Intramolecular Diels–Alder Reaction and Elimination of HCl: One-Pot Approach to Arene-Fused Isoindolinones. European Journal of Organic Chemistry, 2017(30), 4379–4388. https://doi.org/10.1002/ejoc.201700747
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