Category: 103-25-3

An article Cobalt(II)-Catalyzed Alkoxycarbonylation of Aliphatic Amines via C-N Bond Activation WOS:000485089300068 published article about CATALYZED CARBONYLATIVE SYNTHESIS; BENZYLIC AMINES; CROSS-COUPLINGS; ALKYL IODIDES; FUNCTIONALIZATION; TRANSFORMATIONS; HETEROCYCLES; RADICALS; ALCOHOLS in [Li, Chong-Liang; Wu, Xiao-Feng] Zhejiang Sci Tech Univ, Dept Chem, Xiasha Campus, Hangzhou 310018, Peoples R China; [Li, Chong-Liang; Wu, Xiao-Feng] Univ Rostock, Leibniz Inst Katalyse eV, Albert Einstein Str 29a, D-18059 Rostock, Germany; [Jiang, Xuan; Lu, Liang-Qiu; Xiao, Wen-Jing] Cent China Normal Univ, Coll Chem, Minist Educ, Key Lab Pesticide & Chem Biol, 152 Luoyu Rd, Wuhan 430079, Hubei, Peoples R China in 2019.0, Cited 51.0. Recommanded Product: 103-25-3. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

The first cobalt-catalyzed deaminative alkoxycarbonylation reaction was described for the conversion of readily available primary alkyl amines to synthetically versatile esters with moderate to high yields. This transformation shows good functional group compatibility and can serve as a powerful tool for the modification of alkyl amine-containing complex natural products and drug molecules.

Bye, fridends, I hope you can learn more about C10H12O2, If you have any questions, you can browse other blog as well. See you lster.. Recommanded Product: 103-25-3

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

HPLC of Formula: C10H12O2. In 2019.0 GREEN CHEM published article about LIQUID-PHASE HYDROGENATION; HIGHLY-ACTIVE HYDROGENATION; ORGANIC FRAMEWORK NODES; ASYMMETRIC HYDROGENATION; SELECTIVE HYDROGENATION; CATALYTIC-HYDROGENATION; COMPLEXES; ISOOCTENES; KINETICS; CO in [Pews-Davtyan, Anahit; Scharnagl, Florian Korbinian; Hertrich, Maximilian Franz; Kreyenschulte, Carsten; Bartling, Stephan; Lund, Henrik; Jackstell, Ralf; Beller, Matthias] Univ Rostock, Leibniz Inst Katalyse eV, Albert Einstein Str 29a, D-18059 Rostock, Germany in 2019.0, Cited 62.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3.

Catalytic hydrogenation of olefins using noble metal catalysts or pyrophoric RANEY (R) nickel is of high importance in the chemical industry. From the point of view of green and sustainable chemistry, design and development of Earth-abundant, less toxic, and more environmentally friendly catalysts are highly desirable. Herein, we report the convenient preparation of active cobalt catalysts and their application in hydrogenations of a wide range of terminal and internal carbon-carbon double bonds in water under mild conditions. Catalysts are prepared on multi-gram scale by pyrolysis of cobalt acetate and uracil, guanine, adenine or l-tryptophan. The most active material Co-Ura/C-600 showed good productivity in industrially relevant hydrogenation of diisobutene to isooctane and in natural oil hardening.

Welcome to talk about 103-25-3, If you have any questions, you can contact Pews-Davtyan, A; Scharnagl, FK; Hertrich, MF; Kreyenschulte, C; Bartling, S; Lund, H; Jackstell, R; Beller, M or send Email.. HPLC of Formula: C10H12O2

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Iron-catalyzed stereospecific arylation of enol tosylates using Grignard reagents WOS:000508933700018 published article about CROSS-COUPLING REACTIONS; SELECTIVE SYNTHESIS; ALKENYL; EFFICIENT; ALKYNES; ROBUST in [Wei, Yi-Ming; Ma, Xiao-Di; Wang, Lei; Duan, Xin-Fang] Beijing Normal Univ, Coll Chem, Beijing 100875, Peoples R China in 2020.0, Cited 56.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3. Application In Synthesis of Methyl 3-phenylpropionate

The stereospecific Fe-catalyzed arylation of enol tosylates was reported. Various tri- or tetrasubstituted Z or E-enol tosylates of beta-keto esters were arylated using common and Knochel-type Grignard reagents with complete stereofidelity. The precursors for Z/E-zimelidine, tamoxifen and other bioactive compounds were facilely prepared without precious and toxic transition metals.

Application In Synthesis of Methyl 3-phenylpropionate. Welcome to talk about 103-25-3, If you have any questions, you can contact Wei, YM; Ma, XD; Wang, L; Duan, XF or send Email.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Engineering Catalysts for Selective Ester Hydrogenation WOS:000526347200008 published article about TETRADENTATE BIPYRIDINE LIGANDS; OXA-MICHAEL REACTION; RUTHENIUM COMPLEXES; ASYMMETRIC HYDROGENATION; EFFICIENT CATALYSTS; CARBOXYLIC ESTERS; ACID; MECHANISM; LITHIUM; TRIFLUOROACETALDEHYDE in [Dub, Pavel A.; Batrice, Rami J.; Gordon, John C.] Los Alamos Natl Lab, Chem Div, Los Alamos, NM 87545 USA; [Scott, Brian L.] Los Alamos Natl Lab, Mat & Phys Applicat Div, Los Alamos, NM 87545 USA; [Minko, Yury; Schmidt, Jurgen G.; Williams, Robert F.] Los Alamos Natl Lab, Biochem Div, Los Alamos, NM 87545 USA in 2020.0, Cited 116.0. Safety of Methyl 3-phenylpropionate. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

The development of efficient catalysts and processes for synthesizing functionalized (olefinic and/or chiral) primary alcohols and fluoral hemiacetals is currently needed. These are valuable building blocks for pharmaceuticals, agrochemicals, perfumes, and so forth. From an economic standpoint, bench-stable Takasago Int. Corp.’s Ru-PNP, more commonly known as RuMACHO, and Gusev’s Ru-SNS complexes are arguably the most appealing molecular catalysts to access primary alcohols from esters and H-2 (Waser, M. et al. Org. Proc. Res. Dev. 2018, 22, 862). This work introduces economically competitive Ru-SNP(O)(z) complexes (z = 0, 1), which combine key structural elements of both of these catalysts. In particular, the incorporation of SNP heteroatoms into the ligand skeleton was found to be crucial for the design of a more product-selective catalyst in the synthesis of fluoral hemiacetals under kinetically controlled conditions. Based on experimental observations and computational analysis, this paper further extends the current state-of-the-art understanding of the accelerative role of KO-t-C4H9 in ester hydrogenation. It attempts to explain why a maximum turnover is seen to occur starting at similar to 25 mol % base, in contrast to only similar to 10 mol % with ketones as substrates.

Welcome to talk about 103-25-3, If you have any questions, you can contact Dub, PA; Batrice, RJ; Gordon, JC; Scott, BL; Minko, Y; Schmidt, JG; Williams, RF or send Email.. Safety of Methyl 3-phenylpropionate

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Authors Kraevaya, OA; Peregudov, AS; Troyanov, SI; Godovikov, I; Fedorova, NE; Klimova, RR; Sergeeva, VA; Kameneva, LV; Ershova, ES; Martynenko, VM; Claes, S; Kushch, AA; Kostyuk, SV; Schols, D; Shestakov, AF; Troshin, PA in ROYAL SOC CHEMISTRY published article about CHLOROFULLERENE C60CL6; DERIVATIVES; VIRUS; FUNCTIONALIZATION; INHIBITION; CHEMISTRY; BIOLOGY; C-60; 1ST in [Kraevaya, Ol’ga A.; Troshin, Pavel A.] Skolkovo Inst Sci & Technol, Nobel St 3, Moscow 143026, Russia; [Kraevaya, Ol’ga A.; Martynenko, Vyacheslav M.; Shestakov, Alexander F.; Troshin, Pavel A.] RAS, IPCP, Semenov Prospect 1, Chernogolovka 141432, Russia; [Peregudov, Alexander S.; Godovikov, Ivan] RAS, INEOS, Vavylova St 28,B-334, Moscow 119991, Russia; [Troyanov, Sergey I.] Moscow Lomonosov State Univ, Dept Chem, Moscow, Russia; [Fedorova, Natalya E.; Klimova, Regina R.; Kushch, Alla A.] Minist Hlth Russian Federat, Honored Academcian NF Gamaleya Natl Res Ctr Epide, Gamaleya St 18, Moscow 123098, Russia; [Sergeeva, Vasilina A.; Kameneva, Larisa V.; Ershova, Elizaveta S.; Kostyuk, Svetlana V.] RAMS, Res Ctr Med Genet, Moskvoreche St 1, Moscow 115478, Russia; [Claes, Sandra; Schols, Dominique] Katholieke Univ Leuven, Rega Inst Med Res, Herestr 49, B-3000 Leuven, Belgium; [Shestakov, Alexander F.] Moscow Lomonosov State Univ, Fac Fundamental Phys & Chem Engn, GSP 1,1-51 Leninskie Gory, Moscow 119991, Russia in 2019.0, Cited 43.0. Application In Synthesis of Methyl 3-phenylpropionate. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

We report an inversed Arbuzov reaction of the fullerene derivatives C60Ar5Cl with trialkyl phosphites P(OR)(3) producing alkylated fullerene derivatives C60Ar5R (R = Me, Et, iPr, nBu) with almost quantitative yields. This reaction provides a convenient synthetic route for the preparation of a large variety of functionalized fullerene derivatives with tailored properties, e.g. water-soluble compounds demonstrating promising antiviral activities against HCMV, HSV1, HIV and several influenza virus strains.

Application In Synthesis of Methyl 3-phenylpropionate. Bye, fridends, I hope you can learn more about C10H12O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Safety of Methyl 3-phenylpropionate. I found the field of Chemistry very interesting. Saw the article Site-Selective Silylation of Arenes Mediated by Thianthrene S-Oxide published in 2020.0, Reprint Addresses Wang, P (corresponding author), Ctr Excellence Mol Synth, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China.; Wang, P (corresponding author), Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Energy Regulat Mat, Shanghai 200032, Peoples R China.. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate.

The thianthrene S-oxide (TTSO)-mediated site-selective silylation of arenes has been realized via a thianthrenation/Pd-catalyzed silylation sequence. This method features a broad substrate scope and wide functional group tolerance under mild conditions and allows the synthesis of a set of (hetero)arylsilanes with operationally simple manipulations. The application and generality of the approach were further demonstrated by the late-stage functionalization of marketed drugs. This reaction also represents the first example of a Pd-catalyzed silylation reaction of aryl sulfonium salts.

Safety of Methyl 3-phenylpropionate. About Methyl 3-phenylpropionate, If you have any questions, you can contact Wu, YC; Huang, YH; Chen, XY; Wang, P or concate me.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

I found the field of Chemistry very interesting. Saw the article Pd-Catalyzed Selective Carbonylation of gem-Difluoroalkenes: A Practical Synthesis of Difluoromethylated Esters published in 2019.0. SDS of cas: 103-25-3, Reprint Addresses Beller, M (corresponding author), Univ Rostock, Leibniz Inst Katalyse, Albert Einstein Str 29a, D-18059 Rostock, Germany.. The CAS is 103-25-3. Through research, I have a further understanding and discovery of Methyl 3-phenylpropionate

The first catalyst for the alkoxycarbonylation of gem-difluoroalkenes is described. This novel catalytic transformation proceeds in the presence of Pd(acac)(2)/1,2-bis((di-tert-butylphosphan-yl)methyl)benzene (btbpx) (L4) and allows for an efficient and straightforward access to a range of difluoromethylated esters in high yields and regioselectivities. The synthetic utility of the protocol is showcased in the practical synthesis of a Cyclandelate analogue using this methodology as the key step.

SDS of cas: 103-25-3. Welcome to talk about 103-25-3, If you have any questions, you can contact Liu, JW; Yang, J; Ferretti, F; Jackstell, R; Beller, M or send Email.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Engineering Catalysts for Selective Ester Hydrogenation WOS:000526347200008 published article about TETRADENTATE BIPYRIDINE LIGANDS; OXA-MICHAEL REACTION; RUTHENIUM COMPLEXES; ASYMMETRIC HYDROGENATION; EFFICIENT CATALYSTS; CARBOXYLIC ESTERS; ACID; MECHANISM; LITHIUM; TRIFLUOROACETALDEHYDE in [Dub, Pavel A.; Batrice, Rami J.; Gordon, John C.] Los Alamos Natl Lab, Chem Div, Los Alamos, NM 87545 USA; [Scott, Brian L.] Los Alamos Natl Lab, Mat & Phys Applicat Div, Los Alamos, NM 87545 USA; [Minko, Yury; Schmidt, Jurgen G.; Williams, Robert F.] Los Alamos Natl Lab, Biochem Div, Los Alamos, NM 87545 USA in 2020.0, Cited 116.0. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3. Name: Methyl 3-phenylpropionate

The development of efficient catalysts and processes for synthesizing functionalized (olefinic and/or chiral) primary alcohols and fluoral hemiacetals is currently needed. These are valuable building blocks for pharmaceuticals, agrochemicals, perfumes, and so forth. From an economic standpoint, bench-stable Takasago Int. Corp.’s Ru-PNP, more commonly known as RuMACHO, and Gusev’s Ru-SNS complexes are arguably the most appealing molecular catalysts to access primary alcohols from esters and H-2 (Waser, M. et al. Org. Proc. Res. Dev. 2018, 22, 862). This work introduces economically competitive Ru-SNP(O)(z) complexes (z = 0, 1), which combine key structural elements of both of these catalysts. In particular, the incorporation of SNP heteroatoms into the ligand skeleton was found to be crucial for the design of a more product-selective catalyst in the synthesis of fluoral hemiacetals under kinetically controlled conditions. Based on experimental observations and computational analysis, this paper further extends the current state-of-the-art understanding of the accelerative role of KO-t-C4H9 in ester hydrogenation. It attempts to explain why a maximum turnover is seen to occur starting at similar to 25 mol % base, in contrast to only similar to 10 mol % with ketones as substrates.

Name: Methyl 3-phenylpropionate. Welcome to talk about 103-25-3, If you have any questions, you can contact Dub, PA; Batrice, RJ; Gordon, JC; Scott, BL; Minko, Y; Schmidt, JG; Williams, RF or send Email.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

An article Linear-regioselective hydromethoxycarbonylation of styrene using Ru-clusters/CeO2 catalyst WOS:000531430200007 published article about METAL-SUPPORT INTERACTIONS; ISOMERIZING ALKOXYCARBONYLATION; OXIDATIVE DEHYDROGENATION; RU/CEO2 CATALYSTS; ALCOHOLS; EFFICIENT; CERIA; CO; NANOPARTICLES; CEO2 in [An, Jinghua; Wang, Yehong; Zhang, Zhixin; Zhang, Jian; Wang, Feng] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian Natl Lab Clean Energy, Dalian 116023, Liaoning, Peoples R China; [An, Jinghua] Univ Chinese Acad Sci, Beijing 100049, Peoples R China; [Gocyla, Martin; Dunin-Borkowski, Rafal E.] Forschungszentrum Julich, Ernst Ruska Ctr Microscopy & Spect Electron, D-52425 Julich, Germany; [Gocyla, Martin; Dunin-Borkowski, Rafal E.] Forschungszentrum Julich, Peter Grunberg Inst, D-52425 Julich, Germany in 2020.0, Cited 45.0. Safety of Methyl 3-phenylpropionate. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3

Hydroalkoxycarbonylation of olefins has been considered to be one of the most attractive methods to synthesize esters. Controlling the regioselectivities of linear esters (L) and branched esters (B) is a challenging project for researchers working in this reaction. Although most of the attention has been paid to control the regioselectivity through ligand design in homogeneous catalytic systems, study in the area is still limited. Herein, Ru-clusters/CeO2 is employed as a heterogeneous catalyst for the hydromethoxycarbonylation of styrene without any additives. After optimization of the reaction conditions, the conversion of styrene is > 99% with 83% and 12% regioselectivity of linear and branched ester, respectively. By using different supports (CeO2 (nanoparticle), CeO2-rod, and CeO2-cube), three catalysts including Ru-clusters/CeO2, Ru/CeO2-rod, and Ru/CeO2-cube are prepared and applied in the reaction. Structural characterizations demonstrate that the L/B ratio is related to the Ru size of supported Ru catalysts. Further Raman characterization and NH3-TPD demonstrate that the metal-support interaction and the concentration of oxygen vacancy of the catalyst have a great influence on the Ru size. The mechanism and kinetic analysis for this reaction are also investigated in this work. (C) 2020, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

Safety of Methyl 3-phenylpropionate. Welcome to talk about 103-25-3, If you have any questions, you can contact An, JH; Wang, YH; Zhang, ZX; Zhang, J; Gocyla, M; Dunin-Borkowski, RE; Wang, F or send Email.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Tamang, SR; Cozzolino, AF; Findlater, M in [Tamang, Sem Raj; Cozzolino, Anthony F.; Findlater, Michael] Texas Tech Univ, Dept Chem & Biochem, Lubbock, TX 79409 USA published Iron catalysed selective reduction of esters to alcohols in 2019.0, Cited 45.0. Application In Synthesis of Methyl 3-phenylpropionate. The Name is Methyl 3-phenylpropionate. Through research, I have a further understanding and discovery of 103-25-3.

The reaction of (dppBIAN) FeCl2 with 3 equivalents of n-BuLi affords a catalytically active anionic Fe complex; the nature of the anionic complex was probed using EPR and IR experiments and is proposed to involve a dearomatized, radical, ligand scaffold. This complex is an active catalyst for the hydrosilylation of esters to afford alcohols; loadings as low as 1 mol% were employed.

Application In Synthesis of Methyl 3-phenylpropionate. Welcome to talk about 103-25-3, If you have any questions, you can contact Tamang, SR; Cozzolino, AF; Findlater, M or send Email.

Reference:
Patent; SANOFI; US2011/294788; (2011); A1;,
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics