CAS: 877-65-6; (4-(Tert-Butyl)Phenyl)Methanol
该化合物是第三级苯基酒精衍生物,其特征是苯环的副位置上存在一个三丁基乙基乙醇组,这一结构特征增强了其发育障碍和稳定性,使其成为有机合成中的宝贵中间体,特别是用于生产香料,药品和特殊化学品.其高纯度和一贯性能确保了诸如酯化,乙化和氧化等反应的可靠性能. 化合物在标准条件下的低挥发性和对降解的抗药性进一步增强了其在精良化学应用中的效用. 建议适当处理和储存以保持其完整性.
物理性质
MSDS等安全信息
欧盟法规
ECHA物质C&L通报REACH预注册上下游产品
CAS号624286-50-6 (4-tert-butylph... | CAS号939-97-9 对叔丁基苯甲醛 | CAS号18880-00-7 4-叔丁基苄溴 | CAS号107-18-6 烯丙醇 | CAS号108-95-2 苯酚 | CAS号39895-55-1 4-叔丁基苄胺 | CAS号71-43-2 苯 | CAS号1058648-68-2 4-tert-butyl-1-... | CAS号98-51-1 4-叔丁基甲苯 | CAS号105359-79-3 2-(4-tert-butyl... | CAS号56108-12-4 4-(叔丁基)苯甲酰胺 | CAS号78015-86-8 Urea,N,N'-bis[4... | CAS号3288-99-1 对叔丁基苯乙腈 | CAS号939-97-9 对叔丁基苯甲醛 | CAS号808784-70-5 p-tert-butylben... | CAS号4210-32-6 对叔丁基苯甲腈 | CAS号18880-06-3 (4-tert-butylph... | CAS号98-51-1 4-叔丁基甲苯 | CAS号5406-86-0 4-叔丁基苯乙醇合成工艺路线路线简述
- 合成目标产物 4-Tert-Butylbenzyl Alcohol 主要起始原料 Formaldehyde And 4-Tert-Butylphenylboronic Acid
- 26537-19-9 = 877-65-6
反应条件:1.1 Reagents: (Dimethyl Sulfide)Trihydroboron Solvents: 2-Methyltetrahydrofuran; 20 Min,90 °C
标题:Continuous-Flow Amide And Ester Reductions Using Neat Borane Dimethylsulfide Complex
作者:Oetvoes,Sandor B.; Et Al
参考文献:Chemsuschem 日期:2020 卷标:13(7) 页码:1800-1807]
98-73-7 = 877-65-6
反应条件:1.1 Reagents: Lithium Aluminum Hydride Solvents: Tetrahydrofuran; 0 °C; 6 H,0 °C; Overnight,25 °C; 25 °C -> 0 °C1.2 Reagents: Sodium Hydroxide Solvents: Water; 0 °C; 10 Min,0 °C
标题:Tertiary-Butylbenzene Functionalization As A Strategy For β-Sheet Polypeptides
作者:Nisal,Rahul; Et Al
参考文献:Biomacromolecules 日期:2022 卷标:23(6) 页码:2667-2684]
98-73-7 = 877-65-6
反应条件:1.1 Reagents: Phenylsilane Catalysts: 1816266-78-0 Solvents: Tetrahydrofuran; 20 H,30 °C; 30 °C -> Rt1.2 Reagents: Sodium Hydroxide Solvents: Water; 1 H,Rt
标题:Chelating Bis(1,2,3-Triazol-5-Ylidene) Rhodium Complexes: Versatile Catalysts For Hydrosilylation Reactions
作者:Nguyen,Thanh V. Q.; Et Al
参考文献:Advanced Synthesis & Catalysis 日期:2016 卷标:358(3) 页码:452-458]
624286-50-6 = 877-65-6
反应条件:1.1 Reagents: Silica,Water Catalysts: Nafion H Solvents: Hexane; 20 Min,Rt
标题:The Use Of Nafion-H As An Efficient Catalyst For The Deprotection Of Trimethylsilyl Ethers To Their Corresponding Alcohols Under Mild And Heterogeneous Conditions
作者:Zolfigol,Mohammad Ali; Et Al
参考文献:Phosphorus 日期:2004 卷标:179(11) 页码:2189-2193]
1058648-68-2 = 877-65-6
反应条件:1.1 Catalysts: 12-Tungstophosphoric Acid Solvents: Ethanol; 3.5 H,Reflux
标题:H3Pw12O40 - A Selective,Environmentally Benign,And Reusable Catalyst For The Preparation Of Methoxymethyl And Ethoxymethyl Ethers And Their Deprotection Under Mild Conditions
作者:Mohammadpoor-Baltork,Iraj; Et Al
参考文献:Canadian Journal Of Chemistry 日期:2008 卷标:86(8) 页码:831-840]
18880-00-7 = 877-65-6
反应条件:1.1 Reagents: Silica,Sodium Iodide Solvents: Acetone
标题:Oxidative Transformation Of Arylmethyl Bromides And Alcohols With A Combination Of Mesoporous Silica Fsm-16 And Alkali Iodides Under Photoirradiation
作者:Itoh,Akichika; Et Al
参考文献:Organic Letters 日期:2001 卷标:3(17) 页码:2653-2656]
18880-00-7 = 877-65-6
反应条件:1.1 Reagents: Oxygen Catalysts: Eosin Solvents: Dimethyl Sulfoxide; 12 H,25 °C
标题:Metal-Free,Visible-Light Photoredox Catalysis: Transformation Of Arylmethyl Bromides To Alcohols And Aldehydes
作者:Li,Jian; Et Al
参考文献:Rsc Advances 日期:2014 卷标:4(91) 页码:49974-49978]
= 877-65-6
反应条件:1.1 Reagents: Hantzsch Ester,Lithium Tetrafluoroborate Catalysts: Fac-Tris(2-(2-Pyridinyl)Phenyl)Iridium Solvents: Acetone; 2 H,22 - 27 °C
标题:Electrochemical Pinoylation Of Methylarenes: Improving The Scope And Utility Of Benzylic Oxidation Through Mediated Electrolysis
作者:Hoque,Asmaul Md; Et Al
参考文献:Journal Of The American Chemical Society 日期:2022 卷标:144(33) 页码:15295-15302]
39895-55-1 = 877-65-6
反应条件:1.1 Reagents: Methanol Catalysts: Sodium Hydroxide Solvents: Water; 2 H,7 Atm,240 °C1.2 Reagents: Hydrochloric Acid Solvents: Water; Neutralized
标题:Base-Catalyzed Direct Transformation Of Benzylamines Into Benzyl Alcohols
作者:Kanbara,Yutaka; Et Al
参考文献:Synlett 日期:2012 卷标:23(5) 页码:706-710]
1058648-72-8 = 877-65-6
反应条件:1.1 Catalysts: 1-Methylimidazolium Hydrogen Sulfate; 2 Min,120 °C
标题:Microwave-Assisted Rapid And Efficient Deprotection And Direct Esterification And Silylation Of Mom And Eom Ethers Catalyzed By [hmim][hso4] As A Bronsted Acidic Ionic Liquid
作者:Mohammadpoor-Baltork,Iraj; Et Al
参考文献:Monatshefte Fuer Chemie 日期:2010 卷标:141(10) 页码:1083-1088]
1058648-72-8 = 877-65-6
反应条件:1.1 Catalysts: 12-Tungstophosphoric Acid Solvents: Ethanol; 4 H,Reflux
标题:H3Pw12O40 - A Selective,Environmentally Benign,And Reusable Catalyst For The Preparation Of Methoxymethyl And Ethoxymethyl Ethers And Their Deprotection Under Mild Conditions
作者:Mohammadpoor-Baltork,Iraj; Et Al
参考文献:Canadian Journal Of Chemistry 日期:2008 卷标:86(8) 页码:831-840]
32857-63-9 = 877-65-6
反应条件:1.1 Reagents: Sodium Bicarbonate,Ceric Ammonium Nitrate Catalysts: Silver Carbonate,4,4′-Dimethyl [2,2′-Bipyridine]-4,4′-Dicarboxylate Solvents: Acetonitrile,Water; 12 H,55 °C1.2 Reagents: N-Methylformamide Solvents: Water; 12 H,100 °C
标题:Synthesis Of Benzylic Alcohols By Decarboxylative Hydroxylation
作者:Yu,Qian; Et Al
参考文献:Organic Letters 日期:2023 卷标:25(1) 页码:47-52]
3972-65-4 = 877-65-6
反应条件:1.1 Reagents: Butyllithium Solvents: Tetrahydrofuran,Hexane; -78 °C; 1 H,-78 °C1.2 1 H,-78 °C; -78 °C -> Rt; Overnight,Rt1.3 Reagents: Ammonium Chloride Solvents: Water; Rt2.1 Reagents: Sodium Borohydride Solvents: Ethanol; 0 °C; 45 Min,Rt2.2 Reagents: Sodium Hydroxide Solvents: Water; Rt
标题:Formamide-Catalyzed Nucleophilic Substitutions: Mechanistic Insight And Rationalization Of Catalytic Activity
作者:Kohlmeyer,Corinna; Et Al
参考文献:Acs Catalysis 日期:2020 卷标:10(19) 页码:11567-11577]
26537-19-9 = 877-65-6
反应条件:1.1 Reagents: Diethylsilane Catalysts: Potassium Tert-Butoxide,(Sp-5-12)-[n2,N6-Bis(1,1-Dimethylethyl)-2,6-Pyridinedimethanamine-Kn1,Kn2,Kn6]Di... Solvents: Toluene; 20 Min,50 °C; 50 °C -> Rt1.2 Reagents: Hydrochloric Acid Solvents: Tetrahydrofuran; 2 H,Rt
标题:Cobalt-Catalysed Selective Synthesis Of Aldehydes And Alcohols From Esters
作者:Pattanaik,Sandip; Et Al
参考文献:Chemical Communications (Cambridge 日期:2020 卷标:56(53) 页码:7345-7348]
939-97-9 = 877-65-6
反应条件:1.1 Catalysts: Platinum,Copper Solvents: Isopropanol; 3 H,10 Bar,110 °C
标题:Ultrahigh Selective Hydrogenation Of Furfural Enabled By Modularizing Hydrogen Dissociation And Substrate Activation
作者:Wang,Shuai; Et Al
参考文献:Acs Catalysis 日期:2023 卷标:13(13) 页码:8720-8730]
939-97-9 = 877-65-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: Ethanol; 30 Min,Rt1.2 Reagents: Sodium Hydroxide Solvents: Water; Rt
标题:Direct Allylation Of Benzyl Alcohols,Diarylmethanols,And Triarylmethanols Mediated By Xtalfluor-E
作者:Lebleu,Thomas; Et Al
参考文献:Tetrahedron Letters 日期:2017 卷标:58(5) 页码:442-444]
939-97-9 = 877-65-6
反应条件:1.1 Reagents: Sodium Borohydride Solvents: Ethanol; 0 °C -> Rt; 2 - 3 H,Rt1.2 Reagents: Sodium Hydroxide Solvents: Water; 10 Min,Rt
标题:Snar Catalysis Enhanced By An Aromatic Donor-Acceptor Interaction; Facile Access To Chlorinated Polyfluoroarenes
作者:Senaweera,Sameera; Et Al
参考文献:Chemical Communications (Cambridge 日期:2017 卷标:53(54) 页码:7545-7548]
624286-50-6 = 877-65-6
反应条件:1.1 Reagents: Silica,Thionyl Chloride (Silica-Supported),Water Solvents: Hexane; 20 Min,Rt
标题:Deprotection Of Trimethylsilyl Ethers To Corresponding Alcohols Promoted By Silica Chloride: A Heterogeneous And Eco-Friendly Protocol
作者:Bamoniri,A.; Et Al
参考文献:Journal Of The Iranian Chemical Society 日期:2007 卷标:4(3) 页码:332-335]
624286-50-6 = 877-65-6
反应条件:1.1 Reagents: Silica Solvents: Hexane; 18 Min,Rt
标题:The Use Of Silica Sulfuric Acid As An Efficient Catalyst For Deprotection Of Trimethylsilyl Ethers To The Corresponding Alcohols Under Mild And Heterogeneous Conditions
作者:Bamoniri,A.; Et Al
参考文献:Journal Of The Iranian Chemical Society 日期:2006 卷标:3(1) 页码:85-88]
1058648-68-2 = 877-65-6
反应条件:1.1 Catalysts: 1-Methylimidazolium Hydrogen Sulfate; 2.5 Min,120 °C
标题:Microwave-Assisted Rapid And Efficient Deprotection And Direct Esterification And Silylation Of Mom And Eom Ethers Catalyzed By [hmim][hso4] As A Bronsted Acidic Ionic Liquid
作者:Mohammadpoor-Baltork,Iraj; Et Al
参考文献:Monatshefte Fuer Chemie 日期:2010 卷标:141(10) 页码:1083-1088]
18880-00-7 = 877-65-6
反应条件:1.1 Catalysts: Rhodamine B Solvents: Acetonitrile; 10 Min,Rt1.2 Reagents: Potassium Bicarbonate,Water; 34 H,Rt
标题:Visible-Light Driven Hydrolysis Of Benzyl Halides With Water For Preparation Of Benzyl Alcohols
作者:Xu,Jianbin; Et Al
参考文献:Asian Journal Of Organic Chemistry 日期:2019 卷标:8(2) 页码:261-264]
123324-71-0 = 877-65-6
反应条件:1.1 Reagents: Cesium Carbonate Catalysts: Di-μ-Chlorobis(η3-2-Propenyl)Dipalladium,1H-Imidazolium,1-[2,6-Bis(1-Methylethyl)Phenyl]-3-(2-Bromophenyl)-4,5-Dihydro-,... Solvents: Tetrahydrofuran,Water; 2 H,100 °C
标题:Palladium-Catalyzed Arylation Of Aldehydes With Bromo-Substituted 1,3-Diaryl-Imidazoline Carbene Ligand
作者:Yamamoto,Tetsuya; Et Al
参考文献:Tetrahedron 日期:2015 卷标:71(1) 页码:19-26]
3972-65-4 + 118496-00-7 = 877-65-6
反应条件:1.1 Reagents: Magnesium Solvents: Diethyl Ether,Dichloromethane
标题:Stabilization Of Reactive Aldehydes By Complexation With Methylaluminum Bis(2,6-Diphenylphenoxide) And Their Synthetic Application
作者:Maruoka,Keiji; Et Al
参考文献:Journal Of The American Chemical Society 日期:1993 卷标:115(10) 页码:3943-9]
118496-00-7 + 63488-10-8 = 877-65-6 [标题:Reaction Conditions
标题:Product Subclass 4: Aluminum Alkoxides And Phenoxides
作者:Ooi,T.; Et Al
参考文献:Science Of Synthesis 日期:2004 卷标:7 页码:131-195]
1710-98-1 = 877-65-6 [标题:Reaction Conditions
标题:The Synthesis Of Aldehydes By Means Of A Modified Rosenmund Reduction Of Acid Chlorides
作者:Peters,J. A.; Et Al
参考文献:Recueil Des Travaux Chimiques Des Pays-Bas 日期:1981 卷标:100(1) 页码:21-4]
600730-80-1 = 877-65-6
反应条件:1.1 Reagents: N-Methylformamide Solvents: Water; 12 H,100 °C
标题:Synthesis Of Benzylic Alcohols By Decarboxylative Hydroxylation
作者:Yu,Qian; Et Al
参考文献:Organic Letters 日期:2023 卷标:25(1) 页码:47-52]
98-73-7 + 25015-63-8 = 877-65-6
反应条件:1.1 12 H,Rt2.1 Reagents: Silica Solvents: Methanol; 6 H,50 °C
标题:Catalyst-Free Approach For Hydroboration Of Carboxylic Acids Under Mild Conditions
作者:Xu,Xiaojuan; Et Al
参考文献:Acs Omega 日期:2019 卷标:4(4) 页码:6775-6783]
524-38-9 = 877-65-6
反应条件:1.1 Reagents: Pyridine,Borate(1-),Tetrafluoro-,Hydrogen,Compd. With Pyridine (1:1:1),Oxygen Solvents: Acetonitrile,Dichloromethane; 40 - 60 Min,Rt2.1 Reagents: Hantzsch Ester,Lithium Tetrafluoroborate Catalysts: Fac-Tris(2-(2-Pyridinyl)Phenyl)Iridium Solvents: Acetone; 2 H,22 - 27 °C
标题:Electrochemical Pinoylation Of Methylarenes: Improving The Scope And Utility Of Benzylic Oxidation Through Mediated Electrolysis
作者:Hoque,Asmaul Md; Et Al
参考文献:Journal Of The American Chemical Society 日期:2022 卷标:144(33) 页码:15295-15302
对叔丁基氯苄置于sodium Hydroxide,水体系中,用 1,4-二氧六环 作为反应溶剂,化学反应生成 4-叔丁基苄醇
参考文献:Hojo,Masashi; Ueda,Tadaharu; Inoue,Sunao,Journal Of The Chemical Society. Perkin Transactions 2 (2001),2000,# 8,P. 1735-1740
标题:Hojo,Masashi; Ueda,Tadaharu; Inoue,Sunao,Journal Of The Chemical Society. Perkin Transactions 2 (2001),2000,# 8,P. 1735-1740
海关参考信息
- 2902600000-乙苯
2902700000-异丙基苯
2905110000-甲醇
2906210000-苄醇 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:US-10308588-B2
优先权日:2014-12-15
标 题 :Synthesis of amides and amines from aldehydes or ketones by heterogeneous metal catalysis
发明人：CÓRDOVA ARMANDO; PALO-NIETO CARLOS; AFEWERKI SAMSON
权利人:ORGANOFUEL SWEDEN AB
摘要:A mild and efficient synthesis of primary amines and amides from aldehydes or ketones using a heterogeneous metal catalyst and amine donor is disclosed. The initial heterogeneous metal-catalyzed reaction between the carbonyl and the amine donor components is followed by the addition of a suitable acylating agent component in one-pot, thus providing a catalytic one-pot three-component synthesis of amides. Integration of enzyme catalysis allows for eco-friendly one-pot co-catalytic synthesis of amides from aldehyde and ketone substrates, respectively. The process can be applied to asymmetric synthesis or to the co-catalytic one-pot three-component synthesis of capsaicin and its analogues from vanillin or vanillyl alcohol. A co-catalytic reductive amination/dynamic kinetic resolution (dkr) relay sequence for the asymmetric synthesis of optically active amides from ketones is disclosed. Implementation of a catalytic reductive amination/kinetic resolution (kr) relay sequence produces the corresponding optically active amide product and optical active primary amine product with the opposite stereochemistry from the starting ketones.
专利号:US-6172226-B1
优先权日:1993-12-22
标 题:Synthons for the synthesis and deprotection of peptide nucleic acids under mild conditions
发明人：COULL JAMES M; EGHOLM MICHAEL; HODGE RICHARD P; ISMAIL MOHAMED; RAJUR S B
权利人:PERSEPTIVE BIOSYSTEMS INC
摘要:A method is disclosed for preparing novel PNA synthons having protecting groups capable of removal under mild conditions. The PNA synthons are prepared by coupling novel N-substituted nucleobase intermediates having carbamate protection of the exocyclic amino group of the heterocycle to an amino protected backbone or an amino protected backbone ester of the amino acid N-(2-aminoethyl)-glycine. By the method of this invention, the resultant PNA synthons can have orthogonal protection of the carbamate protected nucleobase and the amino protected backbone. The PNA synthons are useful in the synthesis of peptide nucleic acids (PNAs) and other oligomers such as PNA-DNA chimeras, and may be used in automated synthesizers. Novel compositions of matter are also disclosed. In addition, a guanine PNA synthon having selective carbamate protection of the exocyclic 2-amino group with the C6 carbonyl group unprotected is disclosed.
专利号:US-6469133-B2
优先权日:1999-12-13
标题 :Process for the preparation of polymers of dimeric cyclic esters
发明人：BAKER GREGORY L; SMITH III MILTON R
权利人:UNIV MICHIGAN STATE
摘要:The present invention provides a process for the direct synthesis of high melting polymers made from dimeric cyclic esters. In particular, the present invention provides a process for synthesis of polylactic acid (PLA) from racemic materials such as racemic lactide and polymandelide from mandelide. The process further provides racemic metal organic ligand catalysts such as racemic salbinap that catalyzes the polymerization of racemic dimeric cyclic ester monomers to a polylactide stereocomplex. Polymandelide and mixed dimeric cyclic esters are also prepared in the presence of low amounts of water.
专利号:US-6147217-A
优先权日:1997-02-04
标题:Synthesis of terfenadine and derivatives
发明人：SENANAYAKE CHRIS HUGH; FANG QUN KEVIN; WILKINSON SCOTT HAROLD
权利人:SEPRACOR INC
摘要:Processes for preparing compounds having the general formula: ##STR1## wherein R 1a is protected carboxy, carboxy, hydroxymethyl, protected hydroxymethyl, or methyl are disclosed. Processes of the invention begin with a starting material of the general formula IV ##STR2## wherein R 1 and R 2 are as defined in the specification.
专利号:US-2011183958-A1
优先权日:2008-10-17
标 题 :Azetidine derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase
发明人：POWELL DAVID; TRANMER GEOFFREY K
权利人:MERCK FROSST CANADA LTD
摘要:Azetidine derivatives of structural formula I are inhibitors of stearoyl-coenzyme A delta-9 desaturase (SCD). The compounds of the present invention are useful for the prevention and treatment of conditions related to abnormal lipid synthesis and metabolism, including cardiovascular disease; atherosclerosis; obesity; diabetes; neurological disease; Metabolic Syndrome; insulin resistance; cancer; liver steatosis; and non-alcoholic steatohepatitis.
专利号:US-9533957-B2
优先权日:2012-04-06
标题:Tetrazines and method of synthezising the same
发明人：DEVARAJ NEAL K; YANG JUN
权利人:UNIV CALIFORNIA
摘要:Provided herein, inter alia, are compositions and methods of synthesis and detection of tetrazines, e.g., a tetrazine of formula n nand diazonorcaradienes.
网址: http://www.jinandayuchem.com
企业联系电话：0531-87153728👤
地址:济南市济阳区济北生命科技园
企业联系电话：0531-87153728👤
📞济南大宇化工有限公司控股公司 ⚠️参考联系方式
联系人：徐经理
电话：0531-87153728
手机：13805401165
传真：0531-87922099
邮箱：xufeng192@126.com
通信地址: 济南市济阳区济北生命科技园
邮编: 250022
电话：0531-87153728
手机：13805401165
传真：0531-87922099
邮箱：xufeng192@126.com
通信地址: 济南市济阳区济北生命科技园
邮编: 250022
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领，请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实，百琢研不参与任何交易。企业认领注册入口→
地址:济南市济阳区济北生命科技园
⚠️ 未注册 · 未认证企业
备注: 📌 数据来源说明：本展台内容基于各搜索引擎等公开数据整理，仅作展示用途。请用户自行辨别✉️ 若企业需抹除展台内容或有异议， 请通过页面底部联系方式告知我们，我们会尽快处理。
网址: http://www.jinandayuchem.com
企业联系电话：0531-87153728👤
地址:济南市天桥区新材料交易产业园区西副楼
企业联系电话：0531-87153728👤
📞济南大宇化工有限公司 ⚠️参考联系方式
联系人：徐经理
电话：0531-87153728
手机：13805401165
传真：0531-87922099
邮箱：xufeng192@126.com xufeng192@jinandayuchem.com
通信地址: 济南市天桥区新材料交易产业园区西副楼
邮编: 250022
电话：0531-87153728
手机：13805401165
传真：0531-87922099
邮箱：xufeng192@126.com xufeng192@jinandayuchem.com
通信地址: 济南市天桥区新材料交易产业园区西副楼
邮编: 250022
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领，请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实，百琢研不参与任何交易。企业认领注册入口→
地址:济南市天桥区新材料交易产业园区西副楼
⚠️ 未注册 · 未认证企业
备注: 📌 数据来源说明：本展台内容基于各搜索引擎等公开数据整理，仅作展示用途。请用户自行辨别✉️ 若企业需抹除展台内容或有异议， 请通过页面底部联系方式告知我们，我们会尽快处理。
第 1 / 1 页
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
合成参考文献
摘要:Kleoff, M.; Omoregbee, K.; Zimmer, R., Science of Synthesis Knowledge Updates, (2018) 4, 221.
摘要:Riva, R.; Banfi, L.; Basso, A., Science of Synthesis: Multicomponent Reactions, (2013) 1, 407.
摘要:Kaposi, M.; Witt, J.; Cokoja, M.; Kühn, F. E., Science of Synthesis: C-1 Building Blocks in Organic Synthesis, (2013) 2, 298.
摘要:Yi, C. S., Science of Synthesis: Catalytic Transformations via CH Activation, (2015) 1, 253.
摘要:Francke, R.; Prudlik, A.; Little, R. D., Science of Synthesis: Special Topics, (2021) 1, 305.
📝 需求与反馈
尽可能描述清楚需求与问题信息
