期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 69, 期 19, 页码 6474-6477出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo049118e
关键词
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A simple and efficient methodology for the synthesis Of C-2,N-3-disubstituted-4 quinazolones from anilines and N-acylanthranilic acids was developed. The new cyclization conditions are much milder than any other reported protocols and resulted in excellent yields (87-98%) without chromatography.
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