| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1254520 | Chinese Chemical Letters | 2014 | 4 Pages |
Abstract
Tetrahydro-β-carbolines with strictosamide skeleton have been synthesized via intermolecular condensation, selective reduction, and intramolecular cyclization starting from phthalic anhydrides and tryptamine. The reactions are carried out under mild conditions with a wide range of substrates and functional groups.
Graphical abstractStarting from phthalic anhydride and tryptamine, the synthesis of tetrahydro-β-carbolines has been described via intermolecular condensation, selective reduction and intramolecular cyclization.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Yan-Ni Sun, Cui-Ling Wang, Ning Zhang, Zheng Wang, Zhu-Lan Liu, Jian-Li Liu,