Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5279883 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
A rapid, microwave-assisted synthesis of β-carbolines via a successive condensation/cyclization/dehydrogenation approach is described. This methodology involves the coupling of various tryptamines with aromatic aldehydes/glyoxals. The product imine undergoes a Pictet-Spengler cyclization followed by a final dehydrogenation to yield β-carbolines in a three-step domino reaction. The use of the bifunctional catalyst Pd/C/K-10 combined with microwave irradiation enabled the synthesis of β-carbolines in short reaction times and in good to excellent yields.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Aditya Kulkarni, Mohammed Abid, Béla Török, Xudong Huang,