Abstract
The successful use of sulfamic acid as a catalyst in the inter- and intramolecular Inverse Electron Demand Diels-Alder reactions of iminodienes is described. A one-pot synthesis of tetrahydroquinolines was achieved by three component coupling of benzaldehyde and anilines with electron-rich dienophiles such as 2,3-dihydrofuran, dihydropyran and cyclopentadiene catalyzed by sulfamic acid (H 2 NSO 3 H). The intramolecular cycloaddition of imines, derived from O-prenylsalicylaldehyde with anilines catalyzed by sulfamic acid proceeds smoothly and yielded the diastereomeric tetrahydrochromanoquinolines in good yields.
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