| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5212580 | Tetrahedron | 2017 | 8 Pages |
Abstract
Various novel polycyclic thiopyranoindol annulated [3,4-c]quinolone derivatives were synthesized via domino Knoevenagel-hetero-Diels-Alder reactions of indoline-2-thions and novel N-acrylated anthranilaldehydes in refluxing ethanol as a solvent in the presence of 20Â mol% ZnBr2 as a Lewis acid catalyst. All reactions proceed with high yields with excellent regio- and stereoselectivity.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mostafa Kiamehr, Batoul Alipour, Leyla Mohammadkhani, Behzad Jafari, Peter Langer,
![First Page Preview: ZnBr2 catalyzed domino Knoevenagel-hetero-Diels-Alder reaction: An efficient route to polycyclic thiopyranoindol annulated [3,4-c]quinolone derivatives ZnBr2 catalyzed domino Knoevenagel-hetero-Diels-Alder reaction: An efficient route to polycyclic thiopyranoindol annulated [3,4-c]quinolone derivatives](/preview/png/5212580.png)