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I2/CuO-catalyzed tandem cyclization strategy for one-pot synthesis of substituted 2-aminothiozole from easily available aromatic ketones/α,β-unsaturated ketones and thiourea

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成果类型:
期刊论文
作者:
Zhu, Yan-Ping;Yuan, Jing-Jing;Zhao, Qin;Lian, Mi;Gao, Qing-He;...
通讯作者:
Wu, An-Xin(吴安心
作者机构:
[Wu, An-Xin; Gao, Qing-He; Yang, Yan; Liu, Mei-Cai; Lian, Mi; Zhu, Yan-Ping; Yuan, Jing-Jing; Zhao, Qin] Cent China Normal Univ, Key Lab Pesticide & Chem Biol, Minist Educ, Wuhan 430079, Peoples R China.
通讯机构:
[Wu, An-Xin] C
Cent China Normal Univ, Key Lab Pesticide & Chem Biol, Minist Educ, Wuhan 430079, Peoples R China.
语种:
英文
关键词:
2-Aminothiazole;One-pot reaction;Tandem cyclization;alpha-Halogenation ketones;I-2/CuO
期刊:
Tetrahedron
ISSN:
0040-4020
年:
2012
卷:
68
期:
1
页码:
173-178
基金类别:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [20872042, 201032001]; PCSIRTProgram for Changjiang Scholars & Innovative Research Team in University (PCSIRT) [IRT0953]
机构署名:
本校为第一且通讯机构
院系归属:
化学学院
摘要:
A concise and efficient one-pot process from easily available methyl ketones/unsaturated methyl ketones and thiourea was developed for the synthesis of 2-aminothiazoles under the media of I-2/CuO. The method can highly stereoselectivity obtain the E-isomers of 4-ethenyl-2-aminothiazoles (5a-f). All these target molecules were characterized by NMR, HRMS and IR spectra. Furthermore, the target compounds 3c and 5b were further determined by X-ray crystallog...

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