脱氢
废止
芳基
酒
苯甲酰胺
化学
药物化学
有机化学
组合化学
立体化学
催化作用
烷基
作者
P Hima,Michele Tomasini,Albert Poater,Raju Dey
标识
DOI:10.1002/slct.202400468
摘要
Abstract Herein we report an atom‐economical, transition metal‐free method for synthesizing 2‐aryl quinazolinones through a cascade annulation of 2‐amino benzamide and benzyl alcohol. The reaction proceeds via KO t Bu‐mediated acceptorless alcohol dehydrogenation pathways. The procedure tolerates a wide variety of functional groups and provides a convenient method for the synthesis of 2‐aryl quinazolinones. Mechanistic insights by experiments and DFT calculations lead to unveil the reaction mechanism.
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