Synthesis 2004(1): 69-74  
DOI: 10.1055/s-2003-44367
PAPER
© Georg Thieme Verlag Stuttgart · New York

Inter- and Intramolecular Imino Diels-Alder Reactions Catalyzed by Sulfamic Acid: A Mild and Efficient Catalyst for a One-Pot Synthesis of Tetrahydroquinolines

Rajagopal Nagarajan, Chinnan J. Magesh, Paramasivan T. Perumal*
Organic Chemistry Division, Central Leather Research Institute, Adyar, Chennai - 600 020, India
Fax: +91(44)24911589; e-Mail: ptperumal@hotmail.com;
Further Information

Publication History

Received 4 October 2003
Publication Date:
09 December 2003 (online)

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 (H2NSO3H). 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.