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作 者:FAN Chenli HE Xinwei LIAO Kaisheng WANG Cui'e SHANG Yongjia
机构地区:[1]Department of Material Engineering, Wuhu Institute of Technology, Wuhu 241003, P. R. China [2]Key Laboratory of Functional Molecular Solids, Ministry of Education, Anhui Key Laboratory of Molecule-based Materials, College of Chemistry and Materials Science, Anhui Normal University, Wuhu 241000, P. R. China
出 处:《Chemical Research in Chinese Universities》2016年第1期62-67,共6页高等学校化学研究(英文版)
基 金:Supported by the National Natural Science Foundation of China(Nos.21172001, 21372008), the Program for the New Century Excellent Talents in University of China(No.NCET-10-0004) and the Natural Science Foundation of Anhui Province of China(No. 1308085QB39).
摘 要:A convenient and efficient method was developed for the synthesis of naphtho[2,1-blfurans via 4-dimethylaminopyridine(DMAP)-catalyzed cascade reaction of 2-hydroxy-l-naphthaldehydes and a-halogenated ketones in moderate to good yields in the presence of Na2CO3 at 80 ~C for 6 h. The mechanism for this process was briefly discussed with a tentative catalytic cycle proposed. Moreover, this method features organocatalysts and high step-economy, which makes it practical and attractive.A convenient and efficient method was developed for the synthesis of naphtho[2,1-blfurans via 4-dimethylaminopyridine(DMAP)-catalyzed cascade reaction of 2-hydroxy-l-naphthaldehydes and a-halogenated ketones in moderate to good yields in the presence of Na2CO3 at 80 ~C for 6 h. The mechanism for this process was briefly discussed with a tentative catalytic cycle proposed. Moreover, this method features organocatalysts and high step-economy, which makes it practical and attractive.
关 键 词:4-DIMETHYLAMINOPYRIDINE a-Halogenated ketone Cascade reaction Naphthofuran ORGANOCATALYSIS
分 类 号:TQ028.8[化学工程] TN915.05[电子电信—通信与信息系统]
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