CAS: 19898-41-0; H-D-Glu(Obzl)-Obzl

该化合物是一种受保护的谷状酸衍生物,其特点是α-carboxyl和侧链式碳苯基功能中的苯基酯组,以及一个聚苯乙烯反作用器.该化合物主要用于peptide合成,其保护组在混合反应中加强选择性,同时尽量减少侧反应.p-sylate盐形式提高了有机溶剂的溶解性,便利了固相和溶解相合成的处理.在标准的peptide混合条件下,其稳定性使它成为建造复杂的聚苯二酸酯结构的可靠建筑块.在温度氢化条件下可以有选择地清除苯基酯组,允许在多步相合成中有节制的保护.

结构式图片

上下游产品

D-Glutamic acid toluene-4-sulfonic acid benzyl alcoholB°C-Cha-D-Glu(Bzl)-OBzl benzyloxycarbonyl-γ-benzyl-α-L-glutamyl-D-glutamic acid dibenzyl ester benzyloxycarbonyl-α-benzyl-γ-L-glutamyl-D-glutamic acid dibenzyl ester dibenzyl N-[[(1R,S)-1-(N-(9-fluorenylmethoxycarbonyl)amino)ethyl]methoxyphosphinyl]-D-glutamate

合成工艺路线路线简述

    📜D-谷氨酸,对甲苯磺酸,苯甲醇 以 甲苯 用作溶剂,化学反应生成D-谷氨酸双苄酯对甲苯磺酸盐
    参考文献:Synthesis And Structure Reassignment Of Malylglutamate,A Recently Discovered Earthworm Metabolite
    标题:Synthesis And Structure Reassignment Of Malylglutamate,A Recently Discovered Earthworm Metabolite
    摘要:Malylglutamate,A Newly Identified Metabolite In Earthworms,Was Synthesized Using A Traditional Peptide Coupling Approach For Assembling The Amide From Protected Malate And Glutamate Precursors. The Proposed Structure (1) And A Diastereomer Were Synthesized,But Their NMR Spectra Did Not Match The Natural Sample. Further Analysis Of The Natural Sample Using Hmbc Spectroscopy Suggested An Alternative Attachment Of The Malyl Moiety,And Beta-Malylglutamate (2) Diastereomers Were Synthesized,L,L-2 And D,D-2. NMR Spectra Were An Excellent Match With The Natural Sample,And Chiral-Phase Chromatography Was Employed To Identify (-)-Beta-L-Malyl-L-Glutamate (2) As The Isomer Native To Eisenia Fetida.
    Doi:10.1021/acs.Jnatprod.8B01083

    海关参考信息

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献

    合成方法参考DOI号:10.1016/j.ejmech.2008.01.032
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