CAS: 93423-88-2; 1-Ethyl 2-Methyl (S)-Pyrrolidine-1,2-Dicarboxylate

该化合物是一种有机化合物,其特点是五人组成的环状环状结构,有五人环状环状的五分环状金属结构,该化合物有两种与甲基组同化的碳盒状板状,有助于二甲基酯分类."2S"标志表明,对阳极环的第二碳具有特殊的立体化学作用,这对它的生物活动和再活动至关重要.该化合物一般是无色的,无色可粉黄色液体或固体,取决于其纯度和温度.它溶于极地有机溶剂中,在各种化学反应中有用,特别是在合成更复杂的分子时.二甲基(2S)-丙烯-1-2-二异丙基烯酸酯由于它作为手动建筑块的能力,经常用于医药化学和有机合成中.在处理时,应参考安全数据,如任何化学物质一样,以确保在使用期间采取适当的预防措施.

结构式图片

相似化合物

59936-29-7 73323-65-6 145681-01-2

上下游产品

N-tert-butoxycarbonyl-L-phenylalanineN-tert-butoxycarbonyl-L-phenylalanine B°C-Orn(Z)-OH L-proline methyl ester monohydr°Chloride chloroformic acid ethyl ester -1-pyrrolidinecarboxylateethyl (S)-(-)-2--1-pyrrolidinecarboxylate oxazol-2-one7,7-diphenyl-4,5,6,6a-tetrahydro-1H,3H-pyrrolo1,2-coxazol-2-one (S)-(-)-α,α-di(4-vinylphenyl)-2-[(N-ethoxycarbonyl)pyrrolidine]methanol oxazol-2-one7,7-di(2-naphthyl)-4,5,6,6a-tetrahydro-1H,3H-pyrrolo1,2-coxazol-2-one

合成工艺路线路线简述

  • 147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Methanol; 0 °C; Overnight,0 °C -> Rt
    标题:Asymmetric Reduction Of Ketimines With Trichlorosilane Employing An Imidazole Derived Organocatalyst
    作者:Gautier,Francois-Moana; Jones,Simon; Martin,Stephen J.
    参考文献:Organic & Biomolecular Chemistry 日期:2009 卷标:7(2) 页码:229-231]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Methanol; Overnight,Rt
    标题:Catalytic Asymmetric Synthesis Of Optically Active α-Halo-Carbonyl Compounds
    参考文献:World Intellectual Property Organization]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Methanol; 0 °C -> Rt
    标题:Diaryl-2-Pyrrolidinemethanols Catalyzed Enantioselective Epoxidation Of α,β-Enones: New Insight Into The Effect Of Structural Modification Of The Catalyst On Reaction Efficiency
    作者:Lattanzi,Alessandra; Russo,Alessio
    参考文献:Tetrahedron 日期:2006 卷标:62(52) 页码:12264-12269]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate1.2 Solvents: Methanol
    标题:Enantiopure Erythro- And Threo-1-Aryl-1-[2-Pyrrolidinyl]Methanols: Synthesis From L-Proline
    作者:Solladie-Cavallo,Arlette; Azyat,Khalid; Schmitt,Michel; Welter,Richard
    参考文献:Tetrahedron: Asymmetry 日期:2005 卷标:16(5) 页码:1055-1060]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate; 2 H,Rt; 1 H,Rt1.2 Reagents: Sulfuric Acid Solvents: Water; 5 H,Acidified
    标题:Asymmetric Synthesis Of (R)-Fluoxetine: A Practical Approach Using Recyclable And In-Situ Generated Oxazaborolidine Catalyst
    作者:Padiya,Kamlesh; Gagare,Pravin; Gagare,Manjiri; Lal,Bansi
    参考文献:Chinese Journal Of Chemistry 日期:2009 卷标:27(6) 页码:1137-1140]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate; 30 Min,5 °C; 12 H,Rt
    标题:Dual Catalyst System For Asymmetric Alternating Copolymerization Of Carbon Dioxide And Cyclohexene Oxide With Chiral Aluminum Complexes: Lewis Base As Catalyst Activator And Lewis Acid As Monomer Activator
    作者:Nishioka,Kiyoshi; Goto,Hidetoshi; Sugimoto,Hiroshi
    参考文献:Macromolecules (Washington 日期:2012 卷标:45(20) 页码:8172-8192]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Methanol
    标题:Convenient Method For The Synthesis Of N-(Ethyloxycarbonyl) Ester Derivatives From Amino Acids
    作者:Bhaskar,J. V.; Periasamy,Mariappan
    参考文献:Synthetic Communications 日期:1995 卷标:25(10) 页码:1523-30]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Methanol; 7.5 H,0 °C -> Rt
    标题:Chiral Aminophosphines As Catalysts For Enantioselective Double-Michael Indoline Syntheses
    作者:Khong,San N.; Kwon,Ohyun
    参考文献:Molecules 日期:2012 卷标:17 页码:5626-5650]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Methanol
    标题:Diastereospecific Synthesis Of (S,S)-2-Substituted-4,4-Diphenyl-3,1-Oxazabicyclo[3.3.0]Octanes
    作者:Zuo,Gang; Zhang,Qihan; Xu,Jiaxi
    参考文献:Heteroatom Chemistry 日期:2003 卷标:14(1) 页码:42-45]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Methanol; Rt -> 0 °C; 30 Min,0 °C; 4 H,0 °C; 12 H,Rt
    标题:Towards A General Understanding Of Carbonyl-Stabilized Ammonium Ylide-Mediated Epoxidation Reactions
    作者:Novacek,Johanna; Roiser,Lukas; Zielke,Katharina; Robiette,Raphael; Waser,Mario
    参考文献:Chemistry - A European Journal 日期:2016 卷标:22(32) 页码:11422-11428]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate; Rt; Rt -> 0 °C; 2 H,0 °C
    标题:Synthesis And Application Of A Functionalized Resin For Flow Injection/f Aas Copper Determination In Waters
    作者:Cassella,Ricardo J.; Magalhaes,Otto I. B.; Couto,Marcos Tadeu; Lima,Edson Luiz S.; Neves,Marcia Angelica F. S.; Et Al
    参考文献:Talanta 日期:2005 卷标:67(1) 页码:121-128]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Methanol; Overnight,Rt1.2 Solvents: Water1.3 Solvents: Chloroform
    标题:Asymmetric Carbonyl Reduction With Borane Catalyzed By Chiral Phosphinamides Derived From L-Amino Acid
    作者:Li,Kangying; Zhou,Zhenghong; Wang,Lixin; Chen,Qifa; Zhao,Guofeng; Et Al
    参考文献:Tetrahedron: Asymmetry 日期:2003 卷标:14(1) 页码:95-100]

    147-85-3 = 93423-88-2
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Methanol
    标题:Asymmetric Alkenyl Zirconocene/zinc Additions To Aldehydes And Synthetic Efforts Toward Pseudotrienic Acid A
    作者:Jayasuriya,Nilukshi Renuka
    参考文献:2007 卷标:68(9)

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

合成参考文献

参考DOI号:10.1021/jo034228r
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知