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作 者:Shaojun Liu Pei Xie Leifang Wu Jixing Zhao Zhihua Cai Lin He
机构地区:[1]Key Laboratory for Green Processing of Chemical Engineering of Xinjiang Bingtuan,School of Chemistry and Chemical Engineering,Shihezi University,Xinjiang Uygur Autonomous Region 832000,People’s Republic of China [2]Analysis and Testing Center of Shihezi University,Xinjiang Uygur Autonomous Region,832000,China
出 处:《Organic Chemistry Frontiers》2022年第6期1550-1555,共6页有机化学前沿(英文)
基 金:supported by the National Natural Science Foundation of China(No.22161039);the Excellent Young Teachers Plan of Bingtuan(2017CB001 and CZ027203,CZ002203);the International Cooperation Project of Shihezi University(No.GJHZ201801).
摘 要:A facile and transition-metal-free method for the synthesis of 4-amino isoquinolin-1(2H)-ones has beendeveloped. Arynes react with 4,5-disubstituted oxazoles through a tandem Diels–Alder reaction/dehydrogenation–aromatization/tautamerization process to produce 4-amino isoquinolin-1(2H)-ones in moderate to excellent yields. The reaction can be easily scaled up and the product can be transformed to isoquinoline derivatives efficiently.
关 键 词:synthesis TRANSITION
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