高级检索
(3R,4R,5S)-4,5-环氧基-3-(1-乙基丙氧基)-1-环己烯-1-甲酸乙酯的合成[J]. 中国药科大学学报, 2003, (6): 101-102.
引用本文: (3R,4R,5S)-4,5-环氧基-3-(1-乙基丙氧基)-1-环己烯-1-甲酸乙酯的合成[J]. 中国药科大学学报, 2003, (6): 101-102.
Synthesis of Ethyl(3R,4R,5S)-4,5-epoxy-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylate[J]. Journal of China Pharmaceutical University, 2003, (6): 101-102.
Citation: Synthesis of Ethyl(3R,4R,5S)-4,5-epoxy-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylate[J]. Journal of China Pharmaceutical University, 2003, (6): 101-102.

(3R,4R,5S)-4,5-环氧基-3-(1-乙基丙氧基)-1-环己烯-1-甲酸乙酯的合成

Synthesis of Ethyl(3R,4R,5S)-4,5-epoxy-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylate

  • 摘要: 目的:(3R,4R,5S)-4,5-环氧基-3-(1-乙基丙氧基)-1-环己烯-1-甲酸乙酯是合成抗流感病毒新药奥塞米韦的关键中间体,本文对其不对称合成方法进行研究和改进。方法:以(-)莽草酸为起始物,经酯化、转酮化、还原开环、环氧化等6步反应生成立体专一的目标产物。结果:产物的化学结构经FT-IR,^1HNMR和^13CNMR得以确证。结论:本方法较文献方法反应条件温和,产率提高且成本降低。

     

    Abstract: AIM:Ethyl(3R,4R,5S)-4,5-epox y-3-(1-ethylpropoxy)-1-cyclohexene-1-carboxylate is a key intermediate f or the preparation of novel anti-influenza drug oseltamivir and this study is to improve the chiral synthetic procedure of i t. METHOD:Title compound was

     

/

返回文章
返回