700-16-3 = 372-47-4 + 76469-41-5 + 71902-33-5 + 3512-18-3 + 84476-99-3 反应条件:1.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C2.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C 标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates 作者:Zamostna,Lada; Et Al 参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
6485-79-6 = 372-47-4 + 76469-41-5 + 71902-33-5 + 3512-18-3 + 84476-99-3 反应条件:1.1 Solvents: Toluene-D8; 2 H,Rt2.1 Solvents: Toluene; 3 D,Rt3.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C 标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates 作者:Zamostna,Lada; Et Al 参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
617-86-7 = 372-47-4 + 76469-41-5 + 71902-33-5 + 3512-18-3 + 84476-99-3 反应条件:1.1 Solvents: Toluene-D8; -30 °C; 20 H,-15 °C2.1 Solvents: Toluene-D8; 2 H,Rt3.1 Solvents: Toluene; 3 D,Rt4.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C 标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates 作者:Zamostna,Lada; Et Al 参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
6485-79-6 = 372-47-4 + 76469-41-5 + 71902-33-5 + 3512-18-3 + 84476-99-3 反应条件:1.1 Solvents: Toluene-D8; -30 °C; 20 H,-15 °C2.1 Solvents: Toluene-D8; 8 H,Rt -> 50 °C3.1 Solvents: Toluene; 3 D,Rt4.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C 标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates 作者:Zamostna,Lada; Et Al 参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
2875-18-5 = 372-47-4 + 76469-41-5 + 71902-33-5 + 3512-18-3 + 84476-99-3 反应条件:1.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C 标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates 作者:Zamostna,Lada; Et Al 参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
700-16-3 + 99476-19-4 = 372-47-4 + 76469-41-5 + 71902-33-5 + 3512-18-3 + 84476-99-3 反应条件:1.1 Solvents: Toluene; 3 D,Rt2.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C 标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates 作者:Zamostna,Lada; Et Al 参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
= 372-47-4 + 76469-41-5 + 71902-33-5 + 3512-18-3 + 84476-99-3 反应条件:1.1 Solvents: Toluene-D8; 8 H,Rt -> 50 °C2.1 Solvents: Toluene; 3 D,Rt3.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C 标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates 作者:Zamostna,Lada; Et Al 参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142]
= 372-47-4 + 76469-41-5 + 71902-33-5 + 3512-18-3 + 84476-99-3 反应条件:1.1 Solvents: Toluene-D8; 8 H,Rt -> 50 °C2.1 Solvents: Toluene; 3 D,Rt3.1 Reagents: Triethylsilane Catalysts: Di-μ-Hydrobis[1,1′-(1,3-Propanediyl)Bis[1,1-Bis(1-Methylethyl)Phosphine-Kp]]Dirh... Solvents: Benzene-D6; 48 H,Rt -> 50 °C 标题:Catalytic Hydrodefluorination Of Fluoroaromatics With Silanes As Hydrogen Source At A Binuclear Rhodium Complex: Characterization Of Key Intermediates 作者:Zamostna,Lada; Et Al 参考文献:Journal Of Fluorine Chemistry 日期:2013 卷标:155 页码:132-142
3-吡啶基三氟甲磺酸酯置于c94H134O4P2Pd2,Cesium Fluoride体系中,用 甲苯 用作溶剂,化学反应 14.0H,以30%的收率获得3-氟吡啶 参考文献:An Improved Catalyst System For The Pd-Catalyzed Fluorination Of (Hetero)Aryl Triflates 标题:An Improved Catalyst System For The Pd-Catalyzed Fluorination Of (Hetero)Aryl Triflates 摘要:The Stable Pd(0) Species [(1,5-Cyclooctadiene)(L.Pd)(2)] (L = Adbrettphos) Has Been Prepared And Successfully Evaluated As A Precatalyst For The Fluorination Of Aryl Triflates Derived From Biologically Active And Heteroaryl Phenols,Challenging Substrates For Our Previously Reported Catalyst System. Additionally,This Precatalyst Activates At Room Temperature Under Neutral Conditions,Generates 1,5-Cyclooctadiene As The Only Byproduct,And Leads To Overall Cleaner Reaction Profiles. Doi:10.1021/ol402859K
专利号:US-10011567-B1 优先权日:2017-03-09 标题 :Method for the synthesis of acrylate derivatives 发明人:WANG MINGWEN; ZHANG YUE 权利人:INNOSCI LLC 摘要:The present invention provides an improved synthesis of a salt of acrylate derivatives. The synthesis generally includes the preparation of an ester or an amide containing a leaving group followed by the formation of a salt.
专利号:WO-2025122636-A1 优先权日:2023-12-04 标题:Method for the synthesis of acrylate derivatives 发明人:CAICEDO-CARVAJAL CARLOS; KATZ JORDAN; CHOI SEAN 权利人:ORTHOBOND CORP 摘要:The disclosure relates to the synthesis of quaternary salts of various acrylates in high yield and high purity.
专利号:US-12275733-B2 优先权日:2016-11-07 标 题:Substituted pyrido[3,4-b]indoles for the treatment of cartilage disorders 发明人:GRETZKE DIRK; RITZELER OLAF; HEINELT UWE; WEHNER VOLKMAR; SCHMIDT FRIEDEMANN 权利人:SANOFI SA 摘要:The present invention relates to 8-aryl-substituted and 8-heteroaryl-substituted 9H-pyrido[3,4-b]indoles of the formula (I), in which A, E, G, R1 to R6 and R10 are as defined in the claims, which stimulate chondrogenesis and cartilage matrix synthesis and can be used in the treatment of cartilage disorders and conditions in which a regeneration of damaged cartilage is desired, for example joint diseases such as osteoarthritis. The invention furthermore relates to processes for the synthesis of the compounds of the formula (I), their use as pharmaceuticals, and pharmaceutical compositions comprising them.
专利号:US-5591867-A 优先权日:1992-12-04 标 题 :Synthesis of kainic acid 发明人:MONN JAMES A 权利人:LILLY CO ELI 摘要:This invention provides a process for preparing kainic acid and provides intermediates in the synthesis thereof.
专利号:WO-2016005892-A1 优先权日:2014-07-08 标题 :Process for the preparation of substituted polyazamacrocycles 发明人:SANTARELLI SAMUELE; CHIABERGE STEFANO 权利人:ENI SPA 摘要:Process for the preparation of a polyazamacrocycle substituted with at least one aryl or heteroaryl group comprising reacting at least one unsubstituted polyazamacrocycle with at least one halogenated aryl or heteroaryl compound. Said polyazamacrocycle substituted with at least one aryl or heteroaryl group may advantageously be used in the synthesis of anionic or cationic complexes and/or of supramolecular adducts useful in the construction of luminescent solar concentrators (LSCs), which in their turn may advantageously be used together, for example, with photovoltaic cells (or solar cells), or with photoelectrolytic cells, in solar devices (i.e. devices for exploiting solar energy). Moreover, said polyazamacrocycle may be used in other fields such as, for example, the analytical field, the medical or biomedical field, the biological field, the field of detergents (both for household use and for personal care use). Formula I
专利号:US-9676783-B2 优先权日:2008-10-22 标 题:Method of treatment using substituted pyrazolo[1,5-A] pyrimidine compounds 发明人:HAAS JULIA; ANDREWS STEVEN W; JIANG YUTONG; ZHANG GAN 权利人:ARRAY BIOPHARMA INC 摘要:Compounds useful in the synthesis of compounds for treating pain, cancer, inflammation, neurodegenerative disease or Typanosoma cruzi infection in a mammal.