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Visible‐Light‐Induced C2 Alkylation of Heterocyclic N‐Oxides with N‐Hydroxyphthalimide Esters under Metal‐Free Conditions.
- Source :
- Advanced Synthesis & Catalysis; 11/4/2020, Vol. 362 Issue 21, p4707-4715, 9p
- Publication Year :
- 2020
-
Abstract
- A visible‐light‐induced site selective C−H alkylation of heterocyclic N‐oxides with N‐hydroxyphthalimide esters was developed using Eosin Y as the photocatalyst in the presence of Cs2CO3 under redox‐neutral and mild conditions. Using N‐hydroxyphthalimide esters as the radical precursors, quinoline and pyridine N‐oxides were readily coupled with a wide range of primary, secondary, and tertiary radicals to afford the desired alkylated heterocyclic N‐oxides in moderated to excellent yields. Importantly, this reaction protocol also successfully demonstrated its applications for the construction of glycosyl or bioactive natural dehydroabietic acid containing heterocyclic N‐oxides, as well as the pharmaceutical and agrochemical active alkylated quinine‐based functional molecules (potential antimalarial drug). [ABSTRACT FROM AUTHOR]
- Subjects :
- ALKYLATION
EOSIN
MOLECULES
RADICALS (Chemistry)
Subjects
Details
- Language :
- English
- ISSN :
- 16154150
- Volume :
- 362
- Issue :
- 21
- Database :
- Complementary Index
- Journal :
- Advanced Synthesis & Catalysis
- Publication Type :
- Academic Journal
- Accession number :
- 146831054
- Full Text :
- https://doi.org/10.1002/adsc.202000517