Ugi reaction synthesis of oxindole-lactam hybrids as selective butyrylcholinesterase inhibitors
Molecular hybridization is a valuable approach in drug discovery. Combining it with multicomponent reactions is highly desirable, since structurally diverse libraries can be attained efficiently in an eco-friendly manner. In this work, isatin is used as the key building block for the Ugi 4-center 3-...
| Autor principal: | |
|---|---|
| Outros Autores: | , , , , , |
| Formato: | article |
| Idioma: | eng |
| Publicado em: |
2022
|
| Assuntos: | |
| Texto completo: | http://hdl.handle.net/10174/30930 |
| País: | Portugal |
| Oai: | oai:dspace.uevora.pt:10174/30930 |