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作 者:张志豪 姜芯 李清寒[1,2,3] Zhang Zhihao;Jiang Xina;Li Qinghan(College of Chemistry and Environment,Southwest Minzu University,Chengdu 610041;Key Laboratory of General Chemistry of the National Ethnic Affairs Commission,College of Chemistry and Environment,Southwest Minzu University,Chengdu 610041;Key Laboratory of pollution Control Chemistry and Environmental Functional Materials for Qinghai-Tibet Plateau of the National Ethnic Affairs Commission,College of Chemistry and Environment,Southwest Minzu University,Chengdu 610041)
机构地区:[1]西南民族大学化学与环境学院,成都610041 [2]西南民族大学化学与环境学院国家民委基础化学重点实验室,成都610041 [3]西南民族大学化学与环境学院青藏高原污染控制化学与环境功能材料重点实验室,成都610041
出 处:《有机化学》2022年第4期945-964,共20页Chinese Journal of Organic Chemistry
基 金:西南民族大学研究生创新基金(No.CX2020SZ18);四川省科技支撑计划(No.2015NZ0033)资助项目。
摘 要:许多天然产物和具有生物活性的化合物中均含有苯并[b]呋喃结构.苯并[b]呋喃衍生物具有抗病毒、抗癌、杀虫、抗炎镇痛和抗氧化等生物活性,因而受到了药物化学工作者的青睐,并且成为近年来有机合成研究的热点领域之一.目前已有许多有效的合成方法被报道.综述了近十年来,在过渡金属催化及无催化剂的条件下,通过环化或偶联反应制备取代苯并[b]呋喃衍生物的合成研究进展.Benzo[b]furan structure is found in many natural products and bioactive compounds. Benzo[b]furan derivatives have attracted the attention of pharmaceutical chemists because of their antiviral, anticancer, insecticidal and anti inflammatory, analgesic and antioxidant activities. At present, many effective synthetic methods have been reported and become one of the hot topics of organic synthesis research in recent years. The research progress in the synthesis of substituted benzo[b]-furan derivatives by cyclization or coupling reaction under the conditions of transition metal catalysis and catalysts free in recent ten years is reviewed.
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