105-13-5 = 123-11-5 反应条件:1.1C:2048-37-5,C:1109-15-5,S:Mecn,7 H,Rt 标题:Discovery Of The Quinoxalinone-B(C6F5)3.H2O Combo As A Photocatalyst By Acidochromism Strategy: Aerobic Oxidation Of Alcohol,Alkene,And Thiols 作者:By Huang,Jie Et Al 参考文献:Organic Letters 日期:2023 卷标:25(30) 页码:5613-5618]
105-13-5 = 123-11-5 + 38493-59-3 反应条件:1.1R:Me4-Piperidoxyl,R:Nabr,R:Nahco3,S:H2O,S:Ch2Cl2 标题:Lessons From An Array: Using An Electrode Surface To Control The Selectivity Of A Solution-Phase Chemical Reaction 作者:By Feng,Enqi Et Al 参考文献:Angewandte Chemie 日期:2022 卷标:61(10) 页码:E202116351]
105-13-5 = 123-11-5 反应条件:1.1C:39368-32-6,C:Tio2,S:H2O,4 H,Rt 标题:Facile Preparation Of Cubi2O4/tio2 Hetero-Systems Employed For Simulated Solar-Light Selective Oxidation Of 4-Methoxybenzyl Alcohol Model Compound 作者:By Djaballah,Ahmed Malek Et Al 参考文献:Molecular Catalysis 日期:2023 卷标:546 页码:113251]
696-62-8 = 123-11-5 反应条件:1.1R:Phsih3,R:Et3N,C:29934-17-6,C:19437-26-4,S:Dmf,18 H,75°C 标题:Palladium-Catalyzed Reductive Formylation Of Aryl Iodides With Co2 Under Mild Conditions 作者:By Li,Dan Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(8) 页码:5231-5237]
105-13-5 = 123-11-5 反应条件:1.1R:T-Buok,C:2922795-44-4,S:Phme,24 H,50°C 标题:Alcohol Dehydrogenation-Triggered Selective C3-Alkylation Of Indoles By Homogeneous Azo-Aromatic Cobalt Catalysts 作者:By Kamal Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(9) 页码:5827-5843]
637-69-4 = 123-11-5 反应条件:1.1R:O2,C:Nan3,S:H2O,16 H,Rt 标题:Photo-Induced Cleavage Of Alkenes To Carbonyls In Water 作者:By Yue,Xiaoguang Et Al 参考文献:Asian Journal Of Organic Chemistry 日期:2023 卷标:12(6) 页码:E202300124]
104-93-8 = 123-11-5 反应条件:1.1R:T-Buooh,C:64554-19-4,S:Me(Ch2)8Me,37 H,30°C 标题:Selective Peroxygenase-Catalysed Oxidation Of Toluene Derivates To Benzaldehydes 作者:By Wang,Yutong Et Al 参考文献:Chemcatchem 日期:2023 卷标:15(13) 页码:E202300645]
100-06-1 = 123-11-5 反应条件:1.1R:C5H5N,R:Seo2,110°C1.2R:HCL,S:H2O,Ph 22.1R:Bu4N+ -Oac,C:2867607-77-8,C:22693-41-0,S:Clch2Ch2Cl,8 H,35-40°C 标题:Visible-Light Photoredox-Catalyzed Decarboxylation Of α-Oxo Carboxylic Acids To C1-Deuterated Aldehydes And Aldehydes 作者:By Hu,Chun-Hong And Li,Yang 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(10) 页码:6401-6406]
105-13-5 = 123-11-5 反应条件:1.1C:2923917-23-9 (Nonstoichiometric),S:Phme,24 H,343K,1 Atm 标题:Reversible Low-Temperature Redox Activity And Selective Oxidation Catalysis Derived From The Concerted Activation Of Multiple Metal Species On Cr And Rh-Incorporated Ceria Catalysts 作者:By Ikemoto,Satoru Et Al 参考文献:Physical Chemistry Chemical Physics 日期:2019 卷标:21(37) 页码:20868-20877]
105-13-5 = 123-11-5 反应条件:1.1R:Koh,C:2920937-52-4,S:M-C6H4Me2,5 H,120°C 标题:Synthesis And Structural Characterization Of Palladium Pincer Complexes: Sustainable Synthesis Of Benzothiazoles 作者:By Anandaraj,Pennamuthiriyan Et Al 参考文献:Applied Organometallic Chemistry 日期:2023 卷标:37(5) 页码:E7062]
653586-50-6 = 123-11-5 + 82560-12-1 反应条件:1.1 Reagents: Potassium Hydroxide Solvents: Dimethylformamide; -10 °C; 20 Min,-10 °C1.2 Reagents: Hydroxylamine-O-Sulfonic Acid; -10 °C; -10 °C -> Rt; 2 H,Rt 标题:Synthesis And Chemistry Of 3-Tert-Butyl-1,5-Diaminopyrazole 作者:Blake,Alexander J.; Et Al 参考文献:Organic & Biomolecular Chemistry 日期:2003 卷标:1(23) 页码:4268-4274]
530-62-1 + 696-62-8 = 123-11-5 反应条件:1.1S:Thf,15 Min,Rt; 1 H,Rt2.1R:Et3N,C:Pd2(Dba)3,S:Dmf,5 H,70°C 标题:Use Of Carbonyldiimidazole As An Activator Of Formic Acid In A Tris(Dibenzylideneacetone)Dipalladium-Catalyzed Formylation Of Aryl Iodides 作者:By Nadhagopal,Sundar Et Al 参考文献:Synlett 日期:2023 卷标:34(15) 页码:1809-1813]
104-46-1 = 123-11-5 反应条件:1.1R:O2,C:693794-98-8,S:Mecn,12 H,Rt 标题:Visible Light Photocatalysis For Aerobic Oxidative Cleavage Of Alkenes 作者:By Li,Huili Et Al 参考文献:Tetrahedron Letters 日期:2023 卷标:125 页码:154624]
126443-12-7 = 123-11-5 + 13195-79-4 反应条件:1.1R:Bromosuccinimide,C:Cu(Cf3So3)2,S:Me2Co,S:H2O,3 H,Rt2.1C:Cu(Cf3So3)2,C:150529-93-4,S:Me2Co,1 H,Rt2.2R:Bromosuccinimide,30 Min,Rt 标题:Kinetic Resolution Of Electron-Deficient Bromohydrins Via Copper(Ii)-Catalyzed C-C Bond Cleavage 作者:By Choudhary,Kavita Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(16) 页码:12041-12053]
105-13-5 = 123-11-5 反应条件:1.1R:O2,C:2952542-28-6,S:Mecn,12 H,Rt -> 120°C,0.8 Mpa 标题:Additive-Free Selective Oxidation Of Aromatic Alcohols With Molecular Oxygen Catalyzed By A Mixed-Valence Polyoxovanadate-Based Metal-Organic Framework 作者:By Tian,Hongrui Et Al 参考文献:Dalton Transactions 日期:2023 卷标:52(26) 页码:9121-9130]
105-13-5 = 123-11-5 反应条件:1.1R:O2,C:1361312-45-9,C:K2Co3,C:Me4-Piperidoxyl,S:Dmso,6 H,40°C 标题:Copper Pyrithione (Cupt)-Catalyzed Oxidation Of Secondary And Primary Benzyl Alcohols With Molecular Oxygen Or Air Under Mild Conditions 作者:By Peng,Qionghui Et Al 参考文献:Catalysis Letters 日期:2023 卷标:153(9) 页码:2665-2673]
105-13-5 = 123-11-5 反应条件:1.1C:1416881-52-1,C:19788-49-9,S:Acoet,3 H,Rt 标题:Photochemical Hydrogen Atom Transfer Catalysis For Dehydrogenation Of Alcohols To Form Carbonyls 作者:By Yang,Xiaona Et Al 参考文献:Organic Letters 日期:2023 卷标:25(29) 页码:5486-5491]
105-13-5 = 123-11-5 反应条件:1.1S:Mecn,5 H,28°C,1 Bar; 30 Min,28°C 标题:Molten Salt Synthesis Of A Highly Crystalline Graphitic Carbon Nitride Homojunction From A Deep Eutectic Solvent For Selective Photocatalytic Oxidation 作者:By Chen,Yanglin Et Al 参考文献:Journal Of Materials Chemistry A: Materials For Energy And Sustainability 日期:2023 卷标:11(23) 页码:12342-12353]
4180-23-8 = 123-11-5 反应条件:1.1R:R:O2,C:9029-60-1 标题:Co-Oxidative Transformation Of Piperine To Piperonal And 3,4-Methylenedioxycinnamaldehyde By A Lipoxygenase From Pleurotus Sapidus 作者:By Krahe,Nina-Katharina Et Al 参考文献:Chembiochem 日期:2021 卷标:22(19) 页码:2857-2861]
105-13-5 = 123-11-5 反应条件:1.1R:T-Buooh,C:327-97-9 (Complex With Copper),C:Cu (Complex With Chlorogenate),30 Min,45°C 标题:Dual Role Of Chlorogenic Acid As An Influential Precursor In Synthesizing Nano-Sized Cu(Ii) Complexes And Investigating Its Catalytic Role In The Oxidation Of Alcohols And Its Antibacterial Activity 作者:By Shafaghatlonbar,Masoud And Bagherzade,Ghodsieh 参考文献:Journal Of Organometallic Chemistry 日期:2023 卷标:996 页码:122758]
100-09-4 = 123-11-5 反应条件:1.1C:Cucl,C:Me4-Piperidoxyl,S:Dmso 标题:Development And Pilot Scale Implementation Of Safe Aerobic Cu/tempo Oxidation In A Batch Reactor 作者:By Lemaitre,Sylvain Et Al 参考文献:Green Chemistry 日期:2023 卷标:25(14) 页码:5698-5711]
637-69-4 = 123-11-5 反应条件:1.1R:O2,C:2937334-19-3,S:Meoh,S:Mecn,72 H,25°C,0.1 Mpa 标题:Designing Polyoxometalate-Based Metal-Organic Framework For Oxidation Of Styrene And Cycloaddition Of Co2 With Epoxides 作者:By Yan,Xiaomei Et Al 参考文献:Chinese Chemical Letters 日期:2023 卷标:34(7) 页码:107851]
105-13-5 = 123-11-5 反应条件:1.1R:Me4-Piperidoxyl,R:O2,C:Fe(No3)3,S:Acoh,90 H,80°C,1 Bar 标题:Honeycomb Reactor: A Promising Device For Streamlining Aerobic Oxidation Under Continuous-Flow Conditions 作者:By Hosoya,Masahiro Et Al 参考文献:Beilstein Journal Of Organic Chemistry 日期:2023 卷标:19 页码:752-763]
2186-92-7 = 123-11-5 + 115240-92-1 反应条件:1.1C:2515173-80-3 (Deprotected),S:H2O,S:Dmso,2 H,90°C 标题:Mixtures Of Acid- And Base-Functionalized Microparticles For One-Pot Cascade Reaction 作者:By Chen,Chen Et Al 参考文献:Macromolecular Rapid Communications 日期:2023 卷标:44(12) 页码:2300063]
105-13-5 = 123-11-5 反应条件:1.1R:H2O2,C:89485-18-7,4 H,65°C 标题:Selective Oxidation Of Alcohols Promoted By Cis-Dioxomolybdenum (Vi) Ono Complexes 作者:By Liu,Xiaoxia Et Al 参考文献:Afinidad 日期:2023 卷标:80(598) 页码:35-50]
105-13-5 = 123-11-5 反应条件:1.1R:O2,C:20344-49-4,C:Cds,S:Mecn,30 Min,19-21°C; 2 H,19-21°C 标题:Selectively Permeable Feooh Amorphous Layer Coating Cds For Enhancing Photocatalytic Conversion Of Benzyl Alcohol And Selectivity To Benzaldehyde 作者:By Li,Yan Et Al 参考文献:Chemsuschem 日期:2023 卷标:16(9) 页码:E202202355]
105-13-5 = 123-11-5 反应条件:1.1R:T-Buooh,C:2927523-66-6,30 Min,Rt 标题:Quercetin As A Precursor For The Synthesis Of Novel Nanoscale Cu (Ii) Complex As A Catalyst For Alcohol Oxidation With High Antibacterial Activity 作者:By Moodi,Zahra Et Al 参考文献:Bioinorganic Chemistry And Applications 日期:2021 卷标:From Bioinorganic Chemistry And Applications 页码:8818452]
637-69-4 = 123-11-5 反应条件:1.1R:O2,C:15243-48-8,S:Clch2Ch2Cl,14 H,Rt 标题:Visible-Light Photocatalytic Aerobic C=c Bond Cleavage Of Alkenes To Carbonyls By Cspbbr3 Nanocrystals 作者:By Fan,Qiangwen Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(11) 页码:7391-7400]
105-13-5 = 123-11-5 反应条件:1.1R:Koh,C:2924718-43-2,S:Phme,10 H,80°C; 80°C -> 23°C1.2R:HCL,S:H2O 标题:A Catecholaldimine-Based Niii-Complex As An Effective Catalyst For The Direct Conversion Of Alcohols To Trans-Cinnamonitriles And Aldehydes 作者:By Sharma,Vivek Et Al 参考文献:Journal Of Organic Chemistry 日期:2023 卷标:88(11) 页码:7448-7453]
105-13-5 = 123-11-5 反应条件:1.1R:O2,C:7787-59-9,S:Mecn,2 H,Rt 标题:Chelated Ion-Exchange Strategy Toward Biocl Mesoporous Single-Crystalline Nanosheets For Boosting Photocatalytic Selective Aromatic Alcohols Oxidation 作者:By Li,Wei Et Al 参考文献:Advanced Materials (Weinheim 日期:2023 卷标:35(18) 页码:2300396]
403-42-9 + 105-13-5 = 123-11-5 + 81170-13-0 反应条件:1.1 Reagents: 2,6-Lutidine ,Tetrabutylammonium Bromide ,Tetrabutylammonium Perchlorate ,Tempo Solvents: Acetonitrile; 5.5 H,5 °C1.2 Reagents: Hydrochloric Acid Solvents: Water; Acidified 标题:Pairing Electrocarboxylation Of Unsaturated Bonds With Oxidative Transformation Of Alcohol And Amine 作者:Zhang,Xin; Et Al 参考文献:Chemsuschem 日期:2023 卷标:16(19)
专利号:US-11926589-B2 优先权日:2019-07-09 标 题 :Process for the synthesis of non-racemic cyclohexenes 发明人:REISMAN SARAH; ROMBOLA MICHAEL; LADD CAROLYN L; MCLAUGHLIN MARTIN JOHN; ZUEND STEPHAN; GOETZ ROLAND 权利人:BASF CORP; CALIFORNIA INST OF TECHN 摘要:This invention relates to a process for the synthesis of a non-racemic cyclohexene compound of formula (I) by a Diels-Alder reaction of a compound of formula (II) with a compound of formula (III) wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and Y have the meanings as defined in the description in the presence of a catalyst comprising at least one m-valent metal cation M m+ wherein the metal M is selected from Scandium (Sc), Yttrium (Y), Lanthanum (La), Cerium (Ce), Praseodymium (Pr), Neodymium (Nd), Promethium (Pm), Samarium (Sm), Europium (Eu), Gadolinium 15 (Gd), Terbium (Tb), Dysprosium (Dy), Holmium (Ho), Erbium (Er), Thulium (Tm), Ytterbium (Yb), Lutetium (Lu), Gallium (Ga) and Indium (In), and m is an integer of 1, 2 or 3, and a chiral ligand of the formula (IV) wherein R 10a , R 10b , R 10c , R 10d , R 10a′ , R 10b′ , R 10c′ , R 10d′ , Z and Z′ have the meanings as defined in the description.
专利号:US-11866398-B2 优先权日:2018-05-15 标 题:Total synthesis of prostaglandin J natural products by stereoretentive metathesis 发明人:LI JIAMING; CHEN XU; AHMED TONIA S; STOLTZ BRIAN M; GRUBBS ROBERT H 权利人:CALIFORNIA INST OF TECHN 摘要:This invention relates generally to the synthesis of Δ12-Prostaglandin J product using stereoretentive ruthenium olefin metathesis catalysts supported by dithiolate ligands. Δ12-Prostaglandin J products were generated with excellent selectivity (>99% Z) and in moderate to high/good yields (47% to 80% yield; 58% to 80% yield).
专利号:US-10995049-B2 优先权日:2019-07-19 标 题 :Total synthesis of prostaglandin J natural products and their intermediates 发明人:LI JIAMING; XU CHEN; AHMED TONIA S; GRUBBS ROBERT H; STOLTZ BRIAN M 权利人:CALIFORNIA INST OF TECHN 摘要:The present disclosure is directed to methods of preparing prostaglandin J natural products by stereoretentive metatheses reactions and intermediates used in the synthesis of these natural products, including the use of intermediates of Formula (I-A), where R 1 is defined in the specification
专利号:US-7301006-B2 优先权日:2002-07-16 标 题 :Methods and materials for the synthesis of modified peptides 发明人:YOUNG TRAVIS G; KIESSLING LAURA L 权利人:WISCONSIN ALUMNI RES FOUND 摘要:Methods and protected amino acids useful as building blocks (protected monomers) for the synthesis of peptides and proteins that are selectively modified at one or more side-chain hydroxyl groups. Azide-bearing protecting groups allow the selective deprotection of side-chain hydroxyl groups of amino acids after synthesis of a peptide. Reaction conditions for removal of the azide-bearing protecting group can be selected which are substantially orthogonal to those that will remove α-amino protecting groups typically employed in peptide synthesis, such that hydroxyl groups protected with the azide-bearing protecting group remain protected during synthesis of the peptide chain. Various protecting groups which are readily available can be used for protecting potentially reactive side chain groups of amino acids in the peptide or protein to be modified. Preferred side-chain protecting groups are chemically distinguishable from the azide-bearing protecting group and substantially orthogonal reaction conditions can be selected such that side-chain protection of other amino acids is maintained when the azide-bearing protecting group is removed. The use of the azide-bearing protecting group of this invention for one or more hydroxy amino acids during peptide synthesis allows the selective unmasking of those azide-protected side-chain hydroxyl groups and selective modification of the hydroxyl groups that are selectively unmasked. The methods and materials herein are particularly used in synthesis of sulfated, phosphorylated and glycosylated peptides and proteins. Kits and methods of synthesizing a modified peptide or protein using the kits are also provided.
专利号:US-11548898-B2 优先权日:2017-07-06 标题 :Synthesis of halichondrins 发明人:KISHI YOSHITO; AI YANRAN; YE NING; WANG QIAOYI; YAHATA KENZO; ISO Kentaro; NAINI SANTHOSH REDDY; YAMASHITA SHUJI; LEE JIHOON; OHASHI ISAO; FUKUYAMA TAKASHI 权利人:HARVARD COLLEGE; EISAI R&D MAN CO LTD 摘要:The present invention provides methods for the synthesis of ketones involving a Ni/Zr-mediated coupling reaction. The Ni/Zr-mediated ketolization reactions can be used in the synthesis of halichondrins (e.g., halichondrin A, B, C; homohalichondrin A, B, C; norhalichondrin A, B, C), and analogs thereof. Therefore, the present invention also provides synthetic methods useful for the synthesis of halichondrins, and analogs thereof. Also provided herein are compounds (i.e., intermediates) useful in the synthesis of halichondrins, and analogs thereof. In particular, the present invention provides methods and compounds useful in the synthesis of compound of Formula (H3-A).
专利号:US-7183417-B2 优先权日:2004-04-09 标题:Simple stereocontrolled synthesis of salinosporamide A 发明人:COREY ELIAS J 权利人:HARVARD COLLEGE 摘要:A simple and effective stereocontrolled synthesis of salinosporamide A(1) n nhas been developed which follows the pathway outlined in the FIGURE. The process, the first total synthesis of salinosporamide A, is capable of providing the compound in substantial quantities for further biological studies. In addition to the method of Scheme I, the present invention also includes several novel synthetic intermediate compounds, several intermediate steps of the preferred synthetic process; and the uses of these compounds in the preparation of synthetic derivatives of the compound Salinosporamide A. Salinosporamide A is of special interest as a synthetic target because of its protein in vitro cytotoxic activity against many tumor cell lines (IC 50 values of 10 nM or less).
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合成参考文献
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