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α-酮酯和α-酮酰胺的Henry反应
引用本文:王亚军,沈宗旋,张雅文.α-酮酯和α-酮酰胺的Henry反应[J].有机化学,2006,26(9):1291-1294.
作者姓名:王亚军  沈宗旋  张雅文
作者单位:苏州大学化学化工学院,江苏省有机合成重点实验室,苏州,215006
基金项目:江苏省有机合成重点实验室开放课题(No.JSK015)资助项目.
摘    要:用三乙胺催化环状α-酮酯和α-酮酰胺同硝基甲烷的Henry反应, 首次合成了12个多官能团的β-硝基醇, 它们的结构用元素分析、红外光谱和核磁共振进行了表征. 这一反应速度较快, 室温下进行, 条件温和, 产率较好, 是合成多官能团硝基醇的有效方法.

关 键 词:Henry反应  三乙胺  α-酮酯  α-酮酰胺  β-硝基醇
收稿时间:10 17 2005 12:00AM
修稿时间:03 17 2006 12:00AM

Henry Reaction of α-Ketoesters and α-Ketoamides
WANG Ya-Jun,SHEN Zong-Xuan,ZHANG Ya-Wen.Henry Reaction of α-Ketoesters and α-Ketoamides[J].Chinese Journal of Organic Chemistry,2006,26(9):1291-1294.
Authors:WANG Ya-Jun  SHEN Zong-Xuan  ZHANG Ya-Wen
Institution:Key Laboratory of Organic Synthesis of Jiangsu Province, College of Chemistry and Chemical Engineering Suzhou University, Suzhou 215006
Abstract:The Henry reaction of cyclic α-ketoesters and α-ketoamides was achieved using triethylamine as a promoter. Twelve new multi-functional β-nitroalcohols were synthesized. Their structures were confirmed by elemental analyses, IR, 1H NMR or 13C NMR spectroscopy. β-Nitroalcohols were produced in high yields under mild reaction conditions.
Keywords:Henry reaction  triethylamine  α-ketoester  α-ketoamide  β-nitroalcohol
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