Abstract
A facile and efficient strategy for visible light-induced synthesis of quinazolines has been developed via one-pot three-component reaction of 2-aminoaryl ketones, aldehydes and ammonium acetate. This method displays high efficiency and broad substrate tolerance, allowing quick accesses to quinazolines under catalyst-free condition. The results reported herein disclose an important new application of visible light-induced synthesis in the clean synthesis of valuable organic products.
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