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One-pot Sequential Reaction for the Synthesis of Polysubstituted 3-(3-Nitro-2-phenylchroman-4-yl)-3-arylaminoacrylates
作者姓名:Lili Zhang  Jing Sun  Chaoguo Yan
作者单位:College of Chemistry & Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu 225002, China
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.

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One-pot Sequential Reaction for the Synthesis of Polysubstituted 3-(3-Nitro-2-phenylchroman-4-yl)-3-arylaminoacrylates
Lili Zhang,Jing Sun,Chaoguo Yan.One-pot Sequential Reaction for the Synthesis of Polysubstituted 3-(3-Nitro-2-phenylchroman-4-yl)-3-arylaminoacrylates[J].Chinese Journal of Chemistry,2013,31(12):1546-1550.
Authors:《Chinese Journal of Chemistry》
Institution:College of Chemistry & Chemical Engineering, Yangzhou University, Yangzhou, Jiangsu 225002, China
Abstract: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.
Keywords:chromene  propiolate  acrylate  arylamine  one-pot reaction  diastereoselectivity
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