CAS: 476-33-5; (4Br,5S,11Bs)-1,2-Dimethoxy-12-Methyl-5,6,11B,13-Tetrahydro-4Bh-[1,3]Benzodioxolo[5,6-C]Phenanthridin-5-Ol

该化合物是自然产生的藻类,主要产自帕帕夫罗塞亚家族的植物,特别是原生细胞,其特点是结构复杂,包括一个四环框架,其特点是许多异丙酮藻类典型的四环框架,该化合物展示了一系列生物活动,包括止痛,抗炎和潜在的抗癌特性,从而引起了药理研究的兴趣.已知同性激素与各种生物目标相互作用,影响细胞路径,对...

结构式图片

MSDS等安全信息

    上下游产品

    benzyl (4bR,4cR,5aS,10bS)-1,2-dimethoxy-4b,5a,10b,12-tetrahydro[1,3]benzodioxolo[5,6-c]oxireno[a]phenanthridine-11(4cH)-carboxylate benzyl (5S,6R)-6-(3,4-dimethoxy-2-((methoxymethoxy)methyl)phenyl)-5,6-dihydronaphtho[2,3-d][1,3]dioxol-5-ylcarbamate benzyl (5S,6R)-6-[2-(hydroxymethyl)-3,4-dimethoxyphenyl]-5,6-dihydronaphtho[2,3-d][1,3]dioxol-5-ylcarbamate benzyl (4bR,11bS)-1,2-dimethoxy-4b,13-dihydro[1,3]benzodioxolo[5,6-c]phenanthridine-12(11bH)-carboxylate

    合成工艺路线路线简述

      📜2,3-二甲氧基苄醇置于双(乙腈)氯化钯(II) 盐酸,N-溴代丁二酰亚胺(Nbs),Lithium Aluminium Tetrahydride,正丁基锂,四溴化碳,Potassium Tert-Butylate,Sodium Hydride,氯化铵,Caesium Carbonate,对甲苯磺酸,三苯基膦,Lithium Bromide体系中,用 四氢呋喃,1,4-二氧六环,甲醇,正己烷,二氯甲烷,水,N,N-二甲基甲酰胺,异丙醇 作为反应溶剂,化学反应 63.83H,反应生成 β-高白屈菜碱
      参考文献:对苯二氮杂双环烯烃与芳基硼酸的pdii催化不对称开环反应,对映体选择性合成(+)-全曲烯碱.
      标题:对苯二氮杂双环烯烃与芳基硼酸的pdii催化不对称开环反应,对映体选择性合成(+)-全曲烯碱.
      摘要:
      DOI:10.1002/anie.200603945

      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:Concise Enantioselective Total Syntheses Of (+)-Homochelidonine, (+)-Chelamidine, (+)-Chelidonine, (+)-Chelamine And (+)-Norchelidonine By A Pdii-Catalyzed Ring-Opening Strategy
      作者:Matthew J. Fleming,Helen A. Mcmanus,Alena Rudolph,Walter H. Chan,Jérémy Ruiz,Chris Dockendorff,Mark Lautens |发布日期:2008.2.27
      摘要:Ii-Catalyzed Asymmetric Ring-Opening Reaction Of A Meso-Azabicyclic Alkene With An Aryl Boronic Acid As The Key Step. By Screening A Variety Of Functionalized Ortho-Substituted Aryl Boronic Acids, Chiral Ligands And Reaction Conditions We Were Able To Prepare The Requisite Cis-1-Amino-2-Aryldihydronaphthalenes In High Yield And In Up To 90 % Ee. Early Attempts To Complete The Synthesis Of (+)-Homochelidonine

      合成参考文献


      摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
      📝 需求与反馈
      尽可能描述清楚需求与问题信息
      ×

      通知