CAS: 736140-70-8; 1-(4-Methoxycinnamoyl)Pyrrole

结构式图片

上下游产品

4-methoxy-benzaldehyde 1-(1H-pyrrol-1-yl)-2-(triphenylphosphoranylidene)ethanone 1,1'-carbonyldiimidazole (1S,2R,3R)-2-(4-methoxyphenyl)-5-methylene-3-(1H-pyrrole-1-carbonyl)cyclopentanecarbonitrile ((1S,2S)-2-(4-methoxyphenyl)-4-methylenecyclopentyl)(1H-pyrrol-1-yl)methanone ((1S,2S,3R)-2-(4-methoxyphenyl)-4-methylene-3-((trimethylsilyl)ethynyl)cyclopentyl)(1H-pyrrol-1-yl)methanone

合成工艺路线路线简述

    📜二-1H-吡咯-1-基甲酮 以 四氢呋喃,乙醚,甲苯 作为反应溶剂,化学反应 84.0H,反应生成 (2E)-3-(4-甲氧基苯基)-1-(1H-吡咯-1-基)-2-丙烯-1-酮
    参考文献:重复利用wittig烯烃化催化不对称环氧化,再利用废ph3P(o):应用α,β-不饱和n-酰基吡咯作为酯替代物.
    标题:重复利用wittig烯烃化催化不对称环氧化,再利用废ph3P(o):应用α,β-不饱和n-酰基吡咯作为酯替代物.
    摘要:
    DOI:10.1002/anie.200352509

    海关参考信息

    供应商参考报价(招募中)

    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

    主要参考文献

    参考标题:Development Of An Asymmetric Trimethylenemethane Cycloaddition Reaction: Application In The Enantioselective Synthesis Of Highly Substituted Carbocycles
    作者:Barry M. Trost,Steven M. Silverman,James P. Stambuli |发布日期:2011.12.7
    摘要:Azetidine Structures, Is Discussed. The Conditions Developed To Effect An Asymmetric Tmm Reaction Using 2-Trimethylsilylmethyl Allyl Acetate Were Shown To Be Tolerant Of A Wide Variety Of Alkene Acceptors, Providing The Desired Methylenecyclopentanes With High Levels Of Enantioselectivity. The Donor Scope Was Also Explored, And Substituted Systems Were Tolerated, Including One Bearing A Nitrile Moiety. These

    合成参考文献

    参考DOI号:10.1002/anie.200352509
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知