Abstract
(Benzyloxycarbonyl)-protected 3,4-benzo-7-hydroxy-2,9-diazabicyclo[3.3.1]non-7-enes were prepared by one-pot cyclizations of 1,3-bis(silyl enol ethers) with quinazolines. Subsequent hydrogenation resulted in one-pot deprotection and rearrangement to give 2-(2-aminophenyl)-2,3-dihydropyridin-4(1H)-ones.
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