1121-60-4 = 873-69-8 反应条件:1.1 Reagents: Sodium Acetate,Hydroxyamine Hydrochloride Solvents: Ethanol; 2 H,60 °C 标题:Design,Synthesis,Biological Evaluation And Molecular Docking Studies Of Phenylpropanoid Derivatives As Potent Anti-Hepatitis B Virus Agents 作者:Liu,Sheng; Et Al 参考文献:European Journal Of Medicinal Chemistry 日期:2015 卷标:95 页码:473-482]
109-06-8 = 873-69-8 反应条件:1.1 Reagents: Tert-Butyl Nitrite Catalysts: Cupric Acetate,N-Hydroxyphthalimide Solvents: Acetonitrile; 24 H,80 °C 标题:Copper(Ii)-Promoted Direct Conversion Of Methylarenes Into Aromatic Oximes 作者:Yu,Jiatao; Et Al 参考文献:Organic & Biomolecular Chemistry 日期:2015 卷标:13(27) 页码:7397-7401]
1758-54-9 = 873-69-8 反应条件:1.1 Reagents: Sodium Ethoxide,Hydroxyamine Hydrochloride Solvents: Ethanol 标题:2-Pyridyl Ketone Oximes In Iron(Iii) Carboxylate Chemistry: Synthesis,Structural And Physical Studies Of Tetranuclear Clusters Containing The [fe4(μ3-O)2]8+ 'Butterfly' Core 作者:Gkioni,Catherine; Et Al 参考文献:Polyhedron 日期:2009 卷标:28(15) 页码:3221-3226]
72196-03-3 = 873-69-8 反应条件:1.1 Reagents: Water Solvents: Water 标题:Preparation Of Bis(Quaternary Pyridinium Aldoximes) 作者:Joshi,H. C.; Et Al 参考文献:Indian Journal Of Chemistry 日期:1979 卷标:(2) 页码:162-3]
72196-04-4 = 873-69-8 反应条件:1.1 Reagents: Water Solvents: Water 标题:Preparation Of Bis(Quaternary Pyridinium Aldoximes) 作者:Joshi,H. C.; Et Al 参考文献:Indian Journal Of Chemistry 日期:1979 卷标:(2) 页码:162-3]
106-91-2 = 873-69-8 反应条件:1.1 Solvents: Tetrahydrofuran; 24 H,70 °C2.1 Catalysts: Calcium Chloride Solvents: Dimethylformamide; 30 Min,Rt2.2 Reagents: Potassium Carbonate; 1 H,Rt2.3 Solvents: Dimethylformamide; 1 H,Rt; 24 H,Rt 标题:Chemical Modification Of Glycidyl Methacrylate Copolymers With Oximes Containing Pyridine Groups 作者:Sattarzadeh,Sahar; Et Al 参考文献:Pharma Chemica 日期:2012 卷标:4(6) 页码:2340-2346]
65321-24-6 = 873-69-8 + 5424-19-1 + 100-70-9 + 71-50-1 反应条件:1.1 Solvents: Water 标题:Studies On The Decomposition Of Hgg 12 In Aqueous Solution 作者:Eyer,Peter; Et Al 参考文献:Archiv Der Pharmazie (Weinheim 日期:1986 卷标:319(6) 页码:558-66]
873-69-8 = 873-69-8 反应条件:1.1 Solvents: Ethanol; 2 H,60 °C 标题:Synthesis And Anti Pseudomonas Aeruginosa Activity Of Metal Complexes Of Oxime,Semicarbazone And Phenylhydrazone 作者:Hania,Majed M. 参考文献:Material Science Research India 日期:2006 卷标:3 页码:59-62]
3731-51-9 = 873-69-8 反应条件:1.1 Reagents: Oxygen Catalysts: Aldoxime,1,3,5-Trihydroxy-1,3,5-Triazine-2,4,6(1H,3H,5H)-Trione Solvents: Water; 42 H,100 °C 标题:Metal-Free: A Novel And Efficient Aerobic Oxidation Of Primary Amines To Oximes Using N,N',N''-Trihydroxyisocyanuric Acid And Acetaldoxime As Catalysts In Water 作者:Yu,Jiatao; Et Al 参考文献:Synlett 日期:2014 卷标:25(13) 页码:1873-1878]
3731-51-9 = 873-69-8 反应条件:1.1 Reagents: Oxygen Catalysts: Aldoxime,Tempo,Indium Trichloride Solvents: Toluene; 8 H,100 °C 标题:A Novel And Efficient Catalytic System Including Tempo/acetaldoxime/incl3 For Aerobic Oxidation Of Primary Amines To Oximes 作者:Yu,Jiatao; Et Al 参考文献:Tetrahedron Letters 日期:2014 卷标:55(42) 页码:5751-5755]
586-98-1 = 873-69-8 反应条件:1.1 Reagents: Hydrogen Peroxide,Hydroxylamine Catalysts: 2597233-34-4 Solvents: Acetonitrile,Water; 20 Min,Rt; 2 H,Rt -> 70 °C 标题:Dioxido-Vanadium(V) Complex Catalyzed Oxidation Of Alcohols And Tandem Synthesis Of Oximes: A Simple Catalytic Protocol For C-N Bond Formation 作者:Kurbah,Sunshine Dominic 参考文献:Journal Of Coordination Chemistry 日期:2021 卷标:74(4-6) 页码:905-918]
873-69-8 + 106-91-2 = 873-69-8 反应条件:1.1 Catalysts: Calcium Chloride Solvents: Dimethylformamide; 30 Min,Rt1.2 Reagents: Potassium Carbonate; 1 H,Rt1.3 Solvents: Dimethylformamide; 1 H,Rt; 24 H,Rt 标题:Chemical Modification Of Glycidyl Methacrylate Copolymers With Oximes Containing Pyridine Groups 作者:Sattarzadeh,Sahar; Et Al 参考文献:Pharma Chemica 日期:2012 卷标:4(6) 页码:2340-2346]
65321-24-6 = 873-69-8 [标题:Reaction Conditions 标题:Chemical Stability Of The Hagedorn Oximes Hgg-12 And Hi-6 作者:Eyer,Peter; Et Al 参考文献:Archiv Der Pharmazie (Weinheim 日期:1985 卷标:318(10) 页码:938-46]
72196-00-0 = 873-69-8 反应条件:1.1 Reagents: Water Solvents: Water 标题:Preparation Of Bis(Quaternary Pyridinium Aldoximes) 作者:Joshi,H. C.; Et Al 参考文献:Indian Journal Of Chemistry 日期:1979 卷标:(2) 页码:162-3]
873-69-8 = 873-69-8 反应条件:1.1 Reagents: Silica,Thionyl Chloride; 48 H,Reflux1.2 Solvents: Ethyl Acetate; 48 H,Rt 标题:Copper Complex Anchored On Sba-15 Matrix: An Efficient Catalyst In Green Synthesis Of Pyran-Annulated Spirooxindoles In Aqueous Medium 作者:Ghorbani,Sayedhosein; Et Al 参考文献:Journal Of Chemical 日期:2015 卷标:5(3) 页码:2762-2772]
98-98-6 = 873-69-8 反应条件:1.1 Reagents: Pyridine,Hydroxyamine Hydrochloride Solvents: Ethanol; Rt 标题:Laccase-Catalysed Biotransformation Of Collismycin Derivatives. A Novel Enzymatic Approach For The Cleavage Of Oximes 作者:Gonzalez-Sabin,Javier; Et Al 参考文献:Green Chemistry 日期:2016 卷标:18(4) 页码:989-994]
1121-60-4 = 873-69-8 反应条件:1.1 Reagents: Sodium Acetate,Hydroxyamine Hydrochloride Solvents: Ethanol,Water; 10 Min,80 - 90 °C2.1 Solvents: Ethanol; 2 H,60 °C 标题:Synthesis And Anti Pseudomonas Aeruginosa Activity Of Metal Complexes Of Oxime,Semicarbazone And Phenylhydrazone 作者:Hania,Majed M. 参考文献:Material Science Research India 日期:2006 卷标:3 页码:59-62
碳酸甲丙酯置于亚硝酸特丁酯,N-羟基邻苯二甲酰亚胺,Copper Diacetate体系中,用 乙腈 作为反应溶剂,化学反应 24.0H,以73%的收率获得产物2-吡啶甲醛肟 参考文献:Copper(II)-Promoted Direct Conversion Of Methylarenes Into Aromatic Oximes 标题:Copper(II)-Promoted Direct Conversion Of Methylarenes Into Aromatic Oximes 摘要:一个简单高效的催化体系已经开发出来,可以直接将甲基芳烃转化为芳香肟,使用cu(Oac)2作为催化剂,Nhpi(n-羟基邻苯二甲酰亚胺)作为添加剂,叔丁基硝rite(tbn)既作为氮源也作为氧化剂.该过程在温和条件下进行,能够容忍广泛的底物范围,以63-86%的收率获得产物相应的芳香肟. DOI:10.1039/c5Ob00923E
专利号:US-9755163-B2 优先权日:2010-04-30 标 题:Synthesis of four coordinated palladium complexes and their applications in light emitting devices thereof 发明人:LI JIAN; TURNER ERIC 权利人:ARIZONA BOARD OF REGENTS ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIV; ARIZONA BOARD OF REGENTS ACTING FOR OR ON BEHALF OF ARIZONA STATE UNIV 摘要:Synthesis of four coordinated palladium complexes and their applications in light emitting devices thereof.
专利号:US-9324957-B2 优先权日:2010-04-30 标 题:Synthesis of four coordinated gold complexes and their applications in light emitting devices thereof 发明人:LI JIAN; TUMER ERIC 权利人:LI JIAN; TUMER ERIC; UNIV ARIZONA STATE 摘要:Synthesis of four coordinated gold complexes and their applications in light emitting devices thereof.
专利号:US-9550801-B2 优先权日:2009-04-06 标 题:Synthesis of four coordinated platinum complexes and their applications in light emitting devices thereof 发明人:LI JIAN; WANG ZIXING; TURNER ERIC 权利人:ARIZONA BOARD OF REGENTS ACTING FOR AND ON BEHALF OF ARIZONA STATE UNIV 摘要:Platinum complexes that exhibit photoabsorption and photoemission, methods of making such complexes, and applications thereof are disclosed, including optical devices comprising the complexes.
专利号:WO-8601514-A1 优先权日:1984-08-28 标 题 :Solid phase synthesis linkage 发明人:SPROAT BRIAN STEPHEN 权利人:CELLTECH LTD 摘要:A method for the solid phase synthesis of an oligomer in which a first monomer unit is attached to a solid phase by a linkage characterised in that the linkage comprises at least one urethane bridge of formula (I), wherein X is O or S and the nitrogen atom is linked to the solid phase and products for use in this method.
专利号:US-8710210-B2 优先权日:2010-06-30 标题:Method of using N-thio compounds for oligonucleotide synthesis 发明人:HE YIGANG; SOROKIN VICTOR; MAZUR WIESLAW ADAM 权利人:HE YIGANG; SOROKIN VICTOR; MAZUR WIESLAW ADAM; GIRINDUS AMERICA INC 摘要:A method for synthesizing an oligonucleotide which comprises using a sulfurizing agent of general formula (I) for sulfurizing at least one phosphorus internucleotide linkage of a precursor of the oligonucleotide, wherein R is an aryl group or a heteroaryl group, which is bonded to the S-atom through an annular carbon atom; and R 1 and R 2 are independently organic residues, preferably a C1-C20 hydrocarbon residue. The method may further comprise purifying the oligonucleotide. Also included is a process for the synthesis of the sulfurizing agent.
专利号:US-7019127-B2 优先权日:1997-08-13 标 题 :Solution phase synthesis of oligonucleotides 发明人:REESE COLIN BERNARD; SONG QUANLAI 权利人:AVECIA LTD 摘要:A process for the synthesis in solution phase of a phosphorothioate triester is provided. The process comprises the solution phase coupling of an H-phosphonate with an alcohol in the presence of a coupling agent to form an H-phosphonate diester. The H-phosphonate diester is oxidised in situ with a sulfur transfer agent to produce the phosphorothioate triester. Preferably, the H-phosphonate and alcohol are protected nucleosides or oligonucleotides. Oligonucleotide H-phosphonates which can be used in the formation of phosphorothioate triesters are also provided.