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Transition Metal-Catalyzed C-H Activation/Functionalization of 8-Methylquinolines.
- Source :
-
Chemical record (New York, N.Y.) [Chem Rec] 2024 Nov; Vol. 24 (11), pp. e202400116. Date of Electronic Publication: 2024 Oct 18. - Publication Year :
- 2024
-
Abstract
- 8-Methylquinoline is regarded as an ideal substrate to participate in diversely C(sp <superscript>3</superscript> )-H functionalization reactions. The presence of the chelating nitrogen atom enables 8-methylquinoline to easily form cyclometallated complexes with various transition metals, leading to the selective synthesis of functionalized quinolines. Considering the great importance of quinoline cores in medicinal chemistry, in this review article, we have covered the publications related to the C-H activation and functionalization of 8-methylquinoline under transition metal catalysis during the last decade.<br /> (© 2024 The Chemical Society of Japan and Wiley-VCH GmbH.)
Details
- Language :
- English
- ISSN :
- 1528-0691
- Volume :
- 24
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Chemical record (New York, N.Y.)
- Publication Type :
- Academic Journal
- Accession number :
- 39422078
- Full Text :
- https://doi.org/10.1002/tcr.202400116