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摘要
Diversity-oriented synthesis of the biologically intriguing imidazo[1,2-alpha]pyridine-fused isoquinoline systems from readily available starting materials was achieved through the Groebke-Blackburn-Bienayme reaction followed by a gold-catalyzed cyclization strategy. The synthetic approach is characterized by mild reaction conditions and a broad substrate scope, allowing for the rapid construction of structurally complex and diverse heterocycles in moderate to good yields.
- 出版日期2017-5-4
- 单位北京大学
