Category: 100-19-6

An article Composites of palladium nanoparticles and graphene oxide as a highly active and reusable catalyst for the hydrogenation of nitroarenes WOS:000518494800030 published article about NICKEL ALLOY NANOPARTICLES; SODIUM-BOROHYDRIDE; HETEROGENEOUS CATALYST; EFFICIENT CATALYST; CARBON NANOTUBE; DEHYDROGENATION; REDUCTION; POLYMER; NANOSPHERES; BORANE in [Bilgicli, Hayriye Genc; Diler, Fatma; Zengin, Mustafa] Sakarya Univ, Fac Arts & Sci, Dept Chem, Esentepe Campus, TR-54187 Serdivan, Sakarya, Turkey; [Burhan, Hakan; Cellat, Kemal; Kuyuldar, Esra; Sen, Fatih] Dumlupinar Univ, Biochem Dept, Sen Res Grp, Fac Arts & Sci, Evliya Celebi Campus, TR-43100 Kiltahya, Turkey in 2020.0, Cited 48.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Computed Properties of C8H7NO3

Herein, the composite of palladium nanoparticles and graphene oxide (CPG) has been synthesized by a facile and very efficient method that provided chemical selectivity and high catalytic activity. The synthesized CPG was characterized by several techniques such as transmission and high-resolution electron microscopy (TEM and HR-TEM), X-ray diffraction (XRD) and Raman spectroscopy, and Photoelectron spectroscopy (XPS). CPG was tested for selective reduction of nitroarenes at room temperature. After the addition of CPG to the reaction media, catalytic performances were depended upon the cooperative effect of hydrogen activation with Pd nanoparticles, where the lack of electrons favors an excellent performance. Nitroarenes can be bound to the energetically preferred adsorption site for the nitro group in electrically enriched graphene oxide. In addition, the Pd nanoparticles transfer electrons to the graphene oxide which increases the functions of metal and carbon support. CPG exhibits both chemoprotective and high catalytic performance for hydrogenation of nitroarenes at room temperature. Aniline derivatives were obtained with high yields under mild conditions and a practical catalytic system was developed by the use of CPG.

Welcome to talk about 100-19-6, If you have any questions, you can contact Bilgicli, HG; Burhan, H; Diler, F; Cellat, K; Kuyuldar, E; Zengin, M; Sen, F or send Email.. Computed Properties of C8H7NO3

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Cp*Co(III) catalyzed annulation of N-Cbz hydrazones for the redox-neutral synthesis of isoquinolines via C-H/N-N bond activation WOS:000484074000001 published article about H FUNCTIONALIZATION; INTERNAL ALKYNES; EFFICIENT SYNTHESIS; ACCESS in [Subhedar, Dnyaneshwar D.; Deshmukh, Dewal S.; Bhanage, Bhalchandra M.] Inst Chem Technol, Dept Chem, Nathalal Parekh Marg, Mumbai 400019, Maharashtra, India in 2019.0, Cited 41.0. Category: benzodioxans. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A new cascade oxidative cyclization reaction of N-Cbz hydrazones with internal alkynes has been explored for the preparation of isoquinoline derivatives using Cp*Co-III-catalyst through C-H and N-N bond functionalization. N-Cbz hydrazones are rarely explored as directing group for redox-neutral [4 + 2] cyclization reaction through the cyclometallation and this catalyst system does not require any external oxidizing agent, as well as, silver or antimony salt. The current efficient approach has been utilized for the synthesis of different isoquinoline derivatives with good regioselectivity and yields.

Welcome to talk about 100-19-6, If you have any questions, you can contact Subhedar, DD; Deshmukh, DS; Bhanage, BM or send Email.. Category: benzodioxans

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

I found the field of Chemistry very interesting. Saw the article Toward a Greener Barluenga-Valdes Cross-Coupling: Microwave-Promoted C-C Bond Formation with a Pd/PEG/H2O Recyclable Catalytic System published in 2019.0. Name: 1-(4-Nitrophenyl)ethanone, Reprint Addresses Alami, M; Hamze, A (corresponding author), Univ Paris Sud, BioCIS UMR 8076, Univ Paris Saclay,Fac Pharm,CNRS, Equipe Labellisee Ligue Canc,Lab Chim Therapeut, Rue JB Clement, F-92296 Chatenay Malabry, France.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

A green Barluenga-Valdes cross-coupling reaction for the synthesis of 1,1-diarylethylenes using palladium catalysis has been developed. The new catalytic system based on Pd/Xphos-SO3Na or Pd/MeDavephos-CF3SO3 in PEG/H2O under microwave irradiation was found to be the best conditions for this transformation. The recyclability of the palladium catalyst system was also studied, and it was found to be active over nine runs without significant loss in its activity.

Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.. Name: 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Quality Control of 1-(4-Nitrophenyl)ethanone. Fu, Y; Li, QZ; Li, MP; Du, ZY in [Fu, Ying; Li, Quan-Zhou; Li, Ming-Peng; Du, Zhengyin] Northwest Normal Univ, Coll Chem & Chem Engn, 967 Anning East Rd, Lanzhou, Peoples R China published Aerobic alpha-Sulfonylation of Ketones with Zinc Sulfinates in Aqueous Micellar Media: Highly Selective Access to beta-Keto Sulfones in 2020.0, Cited 52.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

An efficient, inexpensive and environmentally friendly synthesis of beta-ketosulfones, via NaI-catalyzed oxidative sulfonylation of ketones with zinc sulfinates, employing ethylene dibromide (EDB) and air as the oxidants, is described. EDB was shown to be a mild organic oxidant to convert NaI into molecular iodine that promote the cross-coupling reactions of zinc sulfinates with ketones, producing beta-ketosulfones. Mechanistic studies indicated that a radical pathway might be involved in the reaction process. The key feature of the present protocol is the far greater solubility of NaI and sulfinates in micellar arrays present in aqueous solution where the oxidative coupling reactions are taking place.

Welcome to talk about 100-19-6, If you have any questions, you can contact Fu, Y; Li, QZ; Li, MP; Du, ZY or send Email.. Quality Control of 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

In 2021 ADV SYNTH CATAL published article about REDUCTIVE N-HETEROCYCLIZATION; ONE-POT SYNTHESIS; 4(3H)-QUINAZOLINONE DERIVATIVES; CYCLIZATION REACTION; O-IODOANILINES; QUINAZOLINONES; CHEMISTRY; CYCLOCARBONYLATION; FLUORINE; AMINES in [Wang, Le-Cheng; Zhang, Yu; Chen, Zhengkai] Zhejiang Sci Tech Univ, Dept Chem, Hangzhou 310018, Peoples R China; [Wu, Xiao-Feng] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Liaoning, Peoples R China; [Wu, Xiao-Feng] Univ Rostock, Leibniz Inst Katalyse eV, Albert Einstein Str 29a, D-18059 Rostock, Germany in 2021, Cited 54. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Formula: C8H7NO3

A procedure on palladium-catalyzed carbonylative reaction of trifluoroacetimidoyl chlorides and nitro compounds for the construction of pharmaceutically valuable 2-(trifluoromethyl)quinazolin-4(3H)-ones has been achieved. In this transformation, Mo(CO)(6) has been used both as a convenient CO source and a reducing reagent. This newly developed protocol is compatible with various nitro compounds and can be readily scaled up to 1 mmol scale.

Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.. Formula: C8H7NO3

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

I found the field of Chemistry very interesting. Saw the article Half-Sandwich Ruthenium Complexes for One-Pot Synthesis of Quinolines and Tetrahydroquinolines: Diverse Catalytic Activity in the Coupled Cyclization and Hydrogenation Process published in 2020.0. Quality Control of 1-(4-Nitrophenyl)ethanone, Reprint Addresses Yao, ZJ (corresponding author), Shanghai Inst Technol, Sch Chem & Environm Engn, Shanghai 201418, Peoples R China.; Yao, ZJ (corresponding author), Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Fujian, Peoples R China.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Four types of half-sandwich ruthenium complexes with an N,O-coordinate mode based on hydroxyindanone-imine ligands have been prepared in good yields. These stable ruthenium complexes exhibited high activity in the catalytic synthesis of quinolines from the reactions of amino alcohols with different 3 types of ketones or secondary alcohols under very mild conditions. Moreover, the methodology for the direct one-pot synthesis of tetrahydroquinoline derivatives from amino alcohols and ketones has been also developed on the basis of the continuous catalytic activity of this ruthenium catalyst in the selective hydrogenation of the obtained quinoline derivatives with a low catalyst loading. The corresponding products, quinolines and tetrahydroquinoline derivatives, were afforded in good to excellent yields. The efficient and diverse catalytic activity of these ruthenium complexes suggested their potential large-scale application. All of the ruthenium complexes were characterized by various spectroscopies to confirm their structures.

Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.. Quality Control of 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Formula: C8H7NO3. Recently I am researching about RING-OPENING POLYMERIZATION; ALKALINE-EARTH METALS; INTRAMOLECULAR HYDROAMINATION; EPSILON-CAPROLACTONE; MAGNESIUM COMPLEXES; EFFICIENT CATALYSTS; HYDRIDE COMPLEXES; ZINC-COMPLEXES; RARE-EARTH; HYDROBORATION, Saw an article supported by the KIT; German Research Foundation (DFG)German Research Foundation (DFG) [INST 40/467-1 FUGG]; Projekt DEAL. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Goswami, B; Feuerstein, TJ; Yadav, R; Koppe, R; Lebedkin, S; Kappes, MM; Roesky, PW. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

The synthesis of calcium complexes ligated by three different chiral iminophosphonamide ligands, L-H (L=[Ph2P{N(R)CH(CH3)Ph}(2)]), L ‘-H (L ‘=[Ph2P{NDipp}{N(R)CH(CH3)Ph}]), (Dipp=2,6-(Pr2C6H3)-Pr-i), and L ”-H (L ”=[Ph2P{N(R)CH(CH3)naph}(2)]), (naph=naphthyl) is presented. The resulting structures [L2Ca], [L ‘ Ca-2], and [L ” Ca-2] represent the first examples of enantiopure homoleptic calcium complexes based on this type of ligands. The calcium complexes show blue-green photoluminescence (PL) in the solid state, which is especially bright at low temperatures. Whereas the emission of [L ” Ca-2] is assigned to the fluorescence of naphthyl groups, the PL of [L2Ca] and [L ‘ Ca-2] is contributed by long-lived phosphorescence and thermally activated delayed fluorescence (TADF), with a strong variation of the PL lifetimes over the temperature range of 5-295 K. Furthermore, an excellent catalytic activity was found for these complexes in hydroboration of ketones at room temperature, although no enantioselectivity was achieved.

Formula: C8H7NO3. Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Product Details of 100-19-6. In 2019.0 ACS CATAL published article about C BOND-CLEAVAGE; AEROBIC OXIDATION; ELECTRON-TRANSFER; ENAMINO ESTERS; FACILE ACCESS; H ACTIVATION; TRANSITION; TEMPO; CYCLIZATION; EFFICIENT in [Zhan, Jun-Long; Wu, Meng-Wei; Wei, Dian; Wei, Bang-Yi; Jiang, Yu; Yu, Wei; Han, Bing] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Gansu, Peoples R China in 2019.0, Cited 140.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

A 4-HO-TEMPO-catalyzed redox strategy for the synthesis of pyridines through the annulation of cyclopropanols and oxime acetates has been developed. This protocol features good functional group tolerance and high chemoselectivity and also promises to be efficient for the late-stage functionalization of skeletons of drugs and natural products. Mechanism studies indicate that the reaction involves the in situ generated alpha,beta-unsaturated ketones and imines as the key intermediates, which are derived from cyclopropanols and oxime acetates via a TEMPO/TEMPOH redox cycle, respectively. The pyridine products are formed as a result of annulation of enones with imines followed by TEMPO-catalyzed oxidative aromatization by excess oxime acetates. This method not only realizes the TEMPO-catalyzed redox reaction but also broadens the frontiers for TEMPO in catalysis.

Product Details of 100-19-6. Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Authors Giboulot, S; Baldino, S; Ballico, M; Figliolia, R; Pothig, A; Zhang, SM; Zuccaccia, D; Baratta, W in AMER CHEMICAL SOC published article about ASYMMETRIC TRANSFER HYDROGENATION; CHEMOSELECTIVE TRANSFER HYDROGENATION; LIGAND BIFUNCTIONAL CATALYSIS; C BOND FORMATION; HOMOGENEOUS RUTHENIUM; MECHANISTIC ASPECTS; 2-(AMINOMETHYL) PYRIDINE; COMPLEXES SYNTHESIS; PHOSPHINE-LIGANDS; OSMIUM COMPLEXES in [Giboulot, Steven; Baldino, Salvatore; Ballico, Maurizio; Figliolia, Rosario; Zhang, Shuanming; Zuccaccia, Daniele; Baratta, Walter] Univ Udine, Dipartimento DI4A, Via Cotonificio 108, I-33100 Udine, Italy; [Baldino, Salvatore] Univ Torino, Dipartimento Chim, Via Pietro Giuria 7, I-10125 Turin, Italy; [Giboulot, Steven] Johnson Matthey, 28 Cambridge Sci Pk,Milton Rd, Cambridge CB4 0FP, England; [Poethig, Alexander] Tech Univ Munich, Dept Chem, Lichtenbergstr 4, D-85747 Garching, Germany; [Poethig, Alexander] Tech Univ Munich, Catalysis Res Ctr, Lichtenbergstr 4, D-85747 Garching, Germany; [Zhang, Shuanming] JITRI, 699 Xuanwu Ave, Nanjing 210008, Jiangsu, Peoples R China in 2019.0, Cited 158.0. Recommanded Product: 1-(4-Nitrophenyl)ethanone. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

The bidentate HCNN dicarbonyl ruthenium complexes trans,cis-[RuCl2(HCNN)(CO)(2)] (1-3) and trans,cis-[RuCl2(ampy)(CO)(2)] (1a) were prepared by reaction of [RuCl2(CO)(2)](n) with 1-[6-(4′-methylphenyl)pyridin-2-yl]methanamine, benzo[h]quinoline (HCNN), and 2-(aminomethyl)pyridine (ampy) ligands. Alternatively, the derivatives 13 were obtained from the reaction of RuCl3 hydrate with HCO2H and HCNN. The pincer CNN cis-[RuCl(CNN)(CO)(2)] (4) was isolated from 1 by reaction with NEt3. The monocarbonyl complexes trans-[RuCl2(HCNN)(PPh3)(CO)] (5-7) were synthesized from [RuCl2(dmf)(PPh3)2(CO)] and HCNN ligands, while the diacetate trans-[Ru(OAc)(2)(HCNN)(PPh3)(CO)] (8) was obtained from [Ru(OAc)(2)(PPh3)(2)(CO)]. Carbonylation of cis-[RuCl(CNN)(PPh3)(2)] with CO afforded the pincer derivatives [RuCl(CNN)(PPh3)(CO)] (9-11). Treatment of 9 with Na[BArf](4) and PPh3 gave the cationic complex trans-[Ru(CNN)(PPh3)(2)(CO)][BAr4f] (12). The dicarbonyl derivatives 1-4, in the presence of PPh3 or PCy3, and the monocarbonyl complexes 5-12 catalyzed the transfer hydrogenation (TH) of acetophenone (a) in 2-propanol at reflux (S/C = 1000100000 and TOF up to 100000 h(-1)). Compounds 13, with PCy3, and 6 and 8-10 were proven to catalyze the TH of carbonyl compounds, including alpha,beta-unsaturated aldehydes and bulky ketones (S/C and TOF up to 10000 and 100000 h(-1), respectively). The derivatives 1-3 with PCy3 and 5 and 6 catalyzed the hydrogenation (HY) of a (H-2, 30 bar) at 70 degrees C (S/C = 2000-10000). Complex 5 was active in the HY of diaryl ketones and aryl methyl ketones, leading to complete conversion at S/C = 10000.

Welcome to talk about 100-19-6, If you have any questions, you can contact Giboulot, S; Baldino, S; Ballico, M; Figliolia, R; Pothig, A; Zhang, SM; Zuccaccia, D; Baratta, W or send Email.. Recommanded Product: 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Chemoselective Hydrogenation of 4-Nitrostyrene to 4-Aminostyrene by Highly Efficient TiO2 Supported Ni3Sn2 Alloy Catalyst WOS:000462602700003 published article about SELECTIVE HYDROGENATION; NITRO-COMPOUNDS; PD/SIO2 CATALYSTS; NITROARENES; NANOPARTICLES; REDUCTION; AMINES; SN; CINNAMALDEHYDE; OXIDE in [Yamanaka, Nobutaka; Hara, Takayoshi; Ichikuni, Nobuyuki; Shimazu, Shogo] Chiba Univ, Dept Appl Chem & Biotechnol, Grad Sch Engn, Inage Ku, 1-33 Yayoi Cho, Chiba 2638522, Japan in 2019.0, Cited 40.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Safety of 1-(4-Nitrophenyl)ethanone

Ni3Sn2 alloy catalysts supported on various metal oxides (TiO2, Al2O3, ZrO2, SnO2, and CeO2) were successfully prepared by simple hydrothermal method and then applied to the hydrogenation of 4-nitrostyrene under H-2 3.0 MPa at 423 K. All the supported catalysts hydrogenated the nitro group more preferentially than the olefin group from the initial reaction stages, showing 100% chemoselectivities towards the desired 4-aminostyrene. This may be attributed to sigma-interaction between the oxygen lone pairs in the nitro group and Sn atoms in Ni3Sn2 alloy. By prolonging the reaction times, the 4-aminostyrene yields increased and finally reached the maximum yields. Among the catalysts, Ni3Sn2/TiO2 alloy catalyst showed the highest catalytic activity with remarkably high chemoselectivity towards 4-aminostyrene. The conversion and chemoselectivity were 100% and 79%, respectively, at a reaction time of only 2.5 h. From the physical and chemical characterization of the supported catalysts, it was clear that the catalytic activity was correlated with H-2 uptake. The application of the best catalyst for the hydrogenation of a wide variety of substituted nitroarenes resulted in the chemoselective formation of the corresponding aminoarenes.

Welcome to talk about 100-19-6, If you have any questions, you can contact Yamanaka, N; Hara, T; Ichikuni, N; Shimazu, S or send Email.. Safety of 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem