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(1R,3R)-(-)-1-甲氧基-5,6-亚甲二氧基-3-(3,4,5-三甲氧苯基)-异苯并二氢呋喃的选择性合成
引用本文:李前荣.(1R,3R)-(-)-1-甲氧基-5,6-亚甲二氧基-3-(3,4,5-三甲氧苯基)-异苯并二氢呋喃的选择性合成[J].中国科学技术大学学报,1995(4).
作者姓名:李前荣
摘    要:在LiAlH4及光学活性物质(5R)-孟氧基-2(5H)-呋喃酮(5)存在下,将6-(3′,4′,5′-三甲氧基羟卞基)-胡椒醛二甲缩醛(4)的甲苯溶液加热回流8小时,可得旋光性的(1R,3R)-(-)-1-甲氧基-5,6-亚甲二氧基-3-(3,4,5-三甲氧苯基)-异苯并二氢呋喃晶体(1),产率61.8%.

关 键 词:(1R,3R)-(-)-1-甲氧基-5,6-亚甲二氧基-3-(3,4,5-三甲氧苯基)-异苯并二氢呋喃,选择性合成

Stereospecific Synthesis of (-)-1-(R)-Methoxy-5,6-Methylene Dioxyl-3-(R)-(3,4,5-Trimethoxyphenyl) Isobenzodihydrofuran
Li Qianrong.Stereospecific Synthesis of (-)-1-(R)-Methoxy-5,6-Methylene Dioxyl-3-(R)-(3,4,5-Trimethoxyphenyl) Isobenzodihydrofuran[J].Journal of University of Science and Technology of China,1995(4).
Authors:Li Qianrong
Institution:Structure research Laboratory
Abstract:n the presence of LiAlH4 and optically active (5R)menthyloxy-2(5H)-furanone(5), asolution of 6-(3',4',5'-trimethoxyhydroxyoenzyl) -piperonal dimethyl acetal in toluene is refluxed for 8 hours to afford an optically active crystal of the title name with a yield of 61.8 %.
Keywords:R)-methoxy-5  6-methylene dioxyl-3-(R)-(3  4  5-trimethoxyphenyl) isobenzodihydrofuran  stereospecific Synthesis  
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