期刊
SYNTHESIS-STUTTGART
卷 -, 期 -, 页码 -出版社
GEORG THIEME VERLAG KG
DOI: 10.1055/a-2182-7416
关键词
N -(acyloxy)phthalimides; diazines; radicals; electron donor-acceptor (EDA) complexes; Minisci-type alkylation
A photochemical protocol has been developed for the alkylation of diazines (pyrimidines, pyrazines, and pyridazines) with N-(acyloxy)phthalimides. The process is facilitated by the presence of triethylamine under irradiation with 427-390 nm light, enabling rapid cross-coupling reactions to construct a wide range of alkylated diazines.
A photochemical protocol for the alkylation of diazines (pyrimidines, pyrazines, and pyridazines) with N-(acyloxy)phthalimides has been developed. The process is facilitated by the presence of triethylamine under irradiation with 427-390 nm light; this enables rapid cross-coupling reactions to construct a wide range of alkylated diazines.
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