Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5222369 | Tetrahedron | 2011 | 6 Pages |
Abstract
An efficient one-pot method for the synthesis of tetrahydrothieno[3,2-f]quinolines is described, using the imino Diels-Alder reaction between ethyl-5-aminobenzothiophene-2-carboxylate, aromatic aldehydes and cyclic enol ethers. Furthermore, hydroxyalkyl-substituted tetrahydrothieno[3,2-f]quinolines were synthesized in good yields, by performing the same imino Diels-Alder reaction in absence of aldehydes. The intramolecular aza-Diels-Alder reaction of 5-aminobenzothiophene with o-(allyloxy)benzaldehyde was also performed resulting in the fully oxidized thienoquinoline derivative.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Wim Van Snick, Anastasia Parchina, Wim Dehaen,