International Journal on Minority and Group Rights. Том 10. 2003. С. 203-220
1-(2-Furyl)-3, 4-dihydroisoquinolines, easily prepared from readily available phenethylamines undergo tandem alkylation/[4+2]-cycloaddition with allyl halides. The reaction proceeds via 2-allyl-1-furyl-3, 4- dihydroisoquinolinium salt formation and subsequent intramolecular exo-Diels-Alder reaction of furan with the allyl fragment (IMDAF reaction). The adducts formed include the basic structural element of the isoindolo[1, 2-a]isoquinoline alkaloids jamtine and hirsutine. © 2010 Elsevier Ltd. All rights reserved.