| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1368799 | Bioorganic & Medicinal Chemistry Letters | 2016 | 4 Pages |
Abstract
Diversity-oriented construction of new indolizine scaffolds was accomplished by utilizing domino Knoevenagel condensation/intramolecular aldol cyclization. Biological evaluation revealed anticancer activity of these compounds through inhibition of β-catenin and activation of p53.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Seong-Hee Moon, Youngeun Jung, Seong Hwan Kim, Ikyon Kim,