Abstract
A photochemical protocol for the alkylation of diazines (pyrimidines, pyrazines and pyridazines) with N-(acyloxy)phthalimides has been developed. The process is facilitated in the presence of triethylamine (Et3N) under irradiation with 427-390 nm light, enabling rapid cross-coupling reactions to construct a wide range of alkylated diazines.
Original language | English |
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Journal | Synthesis |
DOIs | |
Publication status | Accepted/In press - 2023 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2023 Georg Thieme Verlag. All rights reserved.
ASJC Scopus Subject Areas
- Catalysis
- Organic Chemistry
Keywords
- diazines
- electron-donoracceptor (EDA) complexes
- Minisci-type alkylation
- N-(acyloxy)phthalimides
- radicals