Synthesis of C4-functionalized 1,2,3,4-tetrahydroacridine-based Pfitzinger acid derivatives in deep eutectic solvents and their biological evaluation as dual cholinesterase and α-glucosidase inhibitors
Herein, we report an efficient strategy for the synthesis of C4-functionalized novel Pfitzinger acid derivatives via C(sp 3 )–H bond functionalization.
Authors
- Thangellapally Shirisha (ORCID: https://orcid.org/0000-0002-4496-8211)
- K. Divakar (ORCID: https://orcid.org/0000-0002-7387-6228)
- Dhurke Kashinath (ORCID: https://orcid.org/0000-0002-2509-0386)
- Subir Majhi (ORCID: https://orcid.org/0009-0001-7132-8017)
Institutions
- National Institute of Technology Warangal (IN)
Publication Details
- Journal
- New Journal of Chemistry
- Published
- 2024-12-12
- DOI
- https://doi.org/10.1039/d4nj04137b
- Citations
- 3
- Primary Topic
- Cholinesterase and Neurodegenerative Diseases
- Type
- article
- Field-Weighted Citation Impact
- 1.34
Funders
- Science and Engineering Research Board