One-pot Sequential Reaction for the Synthesis of Polysubstituted 3-(3-Nitro-2-phenylchroman-4-yl)-3-arylaminoacrylates  

One-pot Sequential Reaction for the Synthesis of Polysubstituted 3-(3-Nitro-2-phenylchroman-4-yl)-3-arylaminoacrylates

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作  者:Lili Zhang Jing Sun Chaoguo Yan 

机构地区:[1]College of Chemistry & Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu 225002, China

出  处:《Chinese Journal of Chemistry》2013年第12期1546-1550,共5页中国化学(英文版)

基  金:This work was financially supported by the National Natural Science Foundation of China,the Priority Academic Program Development of Jiangsu Higher Education Institutions

摘  要:The one-pot sequential reaction of arylamines, methyl propiolate and 2-aryl-3-nitrochromenes without any catalyst in refluxing ethanol afforded the polysubstituted 3-(3-nitro-2-phenylchroman-4-yl)-3-arylaminoacrylates in good yields and with high diastereoselectivity. Reaction mechanism was believed involving the initial formation of β-enamino ester and sequential Michael addition.The one-pot sequential reaction of arylamines, methyl propiolate and 2-aryl-3-nitrochromenes without any catalyst in refluxing ethanol afforded the polysubstituted 3-(3-nitro-2-phenylchroman-4-yl)-3-arylaminoacrylates in good yields and with high diastereoselectivity. Reaction mechanism was believed involving the initial formation of β-enamino ester and sequential Michael addition.

关 键 词:CHROMENE propiolate ACRYLATE ARYLAMINE one-pot reaction DIASTEREOSELECTIVITY 

分 类 号:O625[理学—有机化学] O626.13[理学—化学]

 

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