Abstract
Copper(II) acetate/acetic acid/O2 and potassium iodide/tert-butylhydroperoxide systems are shown to affect the selective oxidation of ring-fused aminals to dihydroquinazolines and quinazolinones, respectively. These methods enable the facile preparation of a number of quinazoline alkaloid natural products and their analogues. © 2013 Richers et al.
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Richers, M. T., Zhao, C., & Seidel, D. (2013). Selective copper(II) acetate and potassium iodide catalyzed oxidation of aminals to dihydroquinazoline and quinazolinone alkaloids. Beilstein Journal of Organic Chemistry, 9, 1194–1201. https://doi.org/10.3762/bjoc.9.135
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