Author: tianli

I found the field of Chemistry very interesting. Saw the article Iron-catalyzed chemoselective hydride transfer reactions published in 2021. HPLC of Formula: C8H10O2, Reprint Addresses Renaud, JL (corresponding author), Normandie Univ, CNRS, UNICAEN, LCMT,ENSICAEN, 6 Blvd Marechal Juin, F-14050 Caen, France.. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol

A Diaminocyclopentadienone iron tricarbonyl complex has been applied in chemoselective hydrogen transfer reductions. This bifunctional iron complex demonstrated a broad applicability in mild conditions in various reactions, such as reduction of aldehydes over ketones, reductive alkylation of various functionalized amines with functionalized aldehydes and reduction of alpha,beta-unsaturated ketones into the corresponding saturated ketones. A broad range of functionalized substrates has been isolated in excellent yields with this practical procedure. (C) 2021 Elsevier Ltd. All rights reserved.

HPLC of Formula: C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Coufourier, S; Ndiaye, D; Gaillard, QG; Bettoni, L; Joly, N; Mbaye, MD; Poater, A; Gaillard, S; Renaud, JL or concate me.

Reference:
Alcohol – Wikipedia,
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An article Stereoselective 1,4-Addition of Primary Alcohols to gamma-Alkoxy-alpha,beta-unsaturated Esters WOS:000572131900002 published article about ASYMMETRIC CONJUGATE ADDITION; ENANTIOSELECTIVE SYNTHESIS; TETRAHYDROPYRAN; HYDRATION; ACIDS in [Inatomi, Saki; Takayanagi, Yuta; Watanabe, Kento; Toita, Akinori; Yamakoshi, Hiroyuki; Nakamura, Seiichi] Nagoya City Univ, Grad Sch Pharmaceut Sci, Mizuho Ku, 3-1 Tanabe Dori, Nagoya, Aichi 4678603, Japan in 2021, Cited 26. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Category: alcohols-buliding-blocks

The scope and limitations of the diastereoselective 1,4-addition reaction of primary alcohols to gamma-alkoxy-alpha,beta-unsaturated esters were investigated. We found that a variety of sodium alkoxides, generated from the corresponding primary alcohols with NaH, underwent 1,4-addition reactions with (E)-enoates in CH(2)Cl(2)at -23 degrees C to give beta-alkoxy esters in modest yields with good to excellentsyn-selectivity, whereas stereoselectivity was not observed with the use of glycerol derivatives as nucleophiles. Cyclic acetal protection was found to play a pivotal role for the reaction to proceed.

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SDS of cas: 105-13-5. Authors Yamamoto, Y; Ota, M; Kodama, S; Michimoto, K; Nomoto, A; Ogawa, A; Furuya, M; Kawakami, K in AMER CHEMICAL SOC published article about in [Yamamoto, Yuki; Ota, Miyuto; Kodama, Shintaro; Michimoto, Kazuki; Nomoto, Akihiro; Ogawa, Akiya] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Sakai, Osaka 5998531, Japan; [Furuya, Mitsunori; Kawakami, Kiminori] Mitsubishi Chem Corp, Sci & Innovat Ctr, Yokohama, Kanagawa 2278502, Japan in 2021, Cited 67. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A green method for the oxidation of alcohols to carboxylic acids was developed using a novel co-catalytic system based on gold, silver, and copper catalysts. This reaction system was conducted under atmospheric oxygen in water and mild conditions to selectively oxidize 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid, as a building block for polyethylene furanoate, which is a 100% bio-based, future alternative to the petroleum-based polyethylene terephthalate. Furthermore, various primary alcohols were conveniently oxidized to their corresponding carboxylic acids in up to quantitative yields.

SDS of cas: 105-13-5. Bye, fridends, I hope you can learn more about C8H10O2, If you have any questions, you can browse other blog as well. See you lster.

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An article Ru(II)-NHC catalysed N-Alkylation of amines with alcohols under solvent-free conditions WOS:000647788800007 published article about RUTHENIUM II COMPLEXES; HETEROCYCLIC-CARBENE; BORROWING HYDROGEN; EFFICIENT CATALYSTS; INTRAMOLECULAR HYDROAMINATION; REDUCTIVE AMINATION; OLEFIN METATHESIS; PINCER COMPLEXES; HIGHLY EFFICIENT; AROMATIC-AMINES in [Karaca, Emine Ozge; Dehimat, Zieneb Imene; Yasar, Sedat; Gurbuz, Nevin; Ozdemir, Ismail] Inonu Univ, Catalysis Res & Applicat Ctr, TR-44280 Malatya, Turkey; [Dehimat, Zieneb Imene; Tebbani, Dahmane] Univ Constantine 1, Dept Chem, Lab Nat Prod Plant Origin & Organ Synth, Fac Exact Sci, Constantine 25000, Algeria; [Yasar, Sedat; Gurbuz, Nevin; Ozdemir, Ismail] Inonu Univ, Fac Sci & Art, Dept Chem, TR-44280 Malatya, Turkey; [Cetinkaya, Bekir] Ege Univ, Dept Chem, TR-35100 Izmir, Turkey in 2021, Cited 82. COA of Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

The reaction of [RuCl2(p-cymene)]2 with in situ prepared Ag-N-heterocyclic carbene (NHC) complexes yields a series of [RuCl2(p-cymene)(NHC)] complexes (2). All of the complexes have been characterised by elemental analysis, and 1H NMR and 13C NMR spectroscopies. These complexes have been tested for the N-alkylation of aromatic amines with arylmethyl alcohols under neat conditions in the presence of KOtBu at 120 ?C. Compounds (2) are stable and have high catalytic/selective activity for the N-alkylation reactions of primary amines to afford secondary amines.

COA of Formula: C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Karaca, EO; Dehimat, ZI; Yasar, S; Gurbuz, N; Tebbani, D; Cetinkaya, B; Ozdemir, I or concate me.

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In 2020 CATAL SCI TECHNOL published article about FACILE SYNTHESIS; REACTANTS ACTIVATION; NO ADSORPTION; DOPED G-C3N4; EFFICIENT; NANOSHEETS; ZIRCONIA; REACTIVITY; VACANCIES; MECHANISM in [Wang, Jiadong; Chen, Ruimin; Yuan, Chaowei; Dong, Fan; Sun, Yanjuan] Chongqing Technol & Business Univ, Coll Environm & Resources, Chongqing Key Lab Catalysis & New Environm Mat, Chongqing 400067, Peoples R China; [Wang, Jiadong; Cui, Wen; He, Ye; Yuan, Chaowei; Sheng, Jianping; Li, Jieyuan; Dong, Fan; Sun, Yanjuan] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Res Ctr Environm Sci & Technol, Chengdu 611731, Peoples R China; [Cui, Wen] Southwest Petr Univ, Sch Mat Sci & Engn, Ctr New Energy Mat & Thchnol, Chengdu 610500, Peoples R China; [Zhan, Yuxin] Chongqing Univ, Coll Mat Sci & Engn, Chongqing 400044, Peoples R China in 2020, Cited 60. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Name: (4-Methoxyphenyl)methanol

Graphitic carbon nitride (g-C3N4, CN for short) is a compelling visible-light responsive photocatalyst. However, its photocatalytic efficiency is low due to the random carrier transfer in planes and insufficient redox potential. Herein, we build oxygen functional group modified sodium-doped carbon nitride (OH/Na co-functionalized carbon nitride) to promote directional transfer of charge carriers for acceleration of separation and enhance redox potential for efficient oxidation of NO in air. Specifically, the function of sodium atoms could control the directional transfer of random carriers from the intralayer to the oxygen functional group-modified surface for the purpose of effectively reducing photogenerated electron-hole recombination. Meanwhile, the modification by oxygen-containing functional groups could adjust the band structure of CN, thereby increasing the oxidation-reduction potential of NO in the photocatalyst. The transformation pathways and reaction mechanism of photocatalytic NO oxidation on CN and OH/Na co-functionalized carbon nitride have also been explicated by ESR spectroscopy and in situ DRIFTS and compared. This work provides a new method for simultaneously controlling the random transfer of carriers and adjusting the energy band structure of CN to optimize its photocatalytic efficiency. It is also possible to extend this strategy to improve the performance of other 2D layered catalysts for photocatalytic oxidation.

Name: (4-Methoxyphenyl)methanol. Welcome to talk about 105-13-5, If you have any questions, you can contact Wang, JD; Cui, W; Chen, RM; He, Y; Yuan, CW; Sheng, JP; Li, JY; Zhan, YX; Dong, F; Sun, YJ or send Email.

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Recently I am researching about CONJUGATED MICROPOROUS POLYMERS; AEROBIC OXIDATION; ORGANIC FRAMEWORKS; CATALYTIC-SYSTEM; SUPPORTED TEMPO; CORE-SHELL; SPHERES; DESIGN, Saw an article supported by the National Key Research and Development Program of China [2017YFF0204602]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21861013]; Natural Science Foundation of Guizhou Province [20185769]; Department of Education of Guizhou Province [YJSCXJH (2019)045]; State Key Laboratory of Physical Chemistry of Solid Surfaces (Xiamen University)Xiamen University [201823]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Shen, YM; Xue, Y; Yan, M; Mao, HL; Cheng, H; Chen, Z; Sui, ZW; Zhu, SB; Yu, XJ; Zhuang, JL. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol. COA of Formula: C8H10O2

A bottom-up approach was developed to prepare TEMPO radical decorated hollow aromatic frameworks (HPAF-TEMPO) by using TEMPO radical functionalized monomers and SiO2 nanospheres as templates. The accessible inner layer, high density of TEMPO sites, and hybrid micro-/mesopores of the HPAF-TEMPO enable the aerobic oxidation of a broad range of alcohols with high efficiency and excellent selectivity.

COA of Formula: C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Shen, YM; Xue, Y; Yan, M; Mao, HL; Cheng, H; Chen, Z; Sui, ZW; Zhu, SB; Yu, XJ; Zhuang, JL or send Email.

Reference:
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Wang, ML; Xu, ZK; Shi, Y; Cai, F; Qiu, JQ; Yang, G; Hua, Z; Chen, T in [Wang, Maolin; Xu, Zhenkai; Shi, Yi; Cai, Fang; Qiu, Jiaqi; Chen, Tao] Zhejiang Sci Tech Univ, Minist Educ, Key Lab Adv Text Mat & Mfg Technol, Hangzhou 310018, Peoples R China; [Wang, Maolin; Xu, Zhenkai; Shi, Yi; Cai, Fang; Qiu, Jiaqi; Chen, Tao] Zhejiang Sci Tech Univ, Minist Educ, Ecodyeing & Finishing Engn Res Ctr, Hangzhou 310018, Peoples R China; [Wang, Maolin; Xu, Zhenkai; Shi, Yi; Cai, Fang; Qiu, Jiaqi; Chen, Tao] Zhejiang Sci Tech Univ, Natl Base Int Sci & Technol Cooperat Text & Consu, Hangzhou 310018, Peoples R China; [Shi, Yi; Cai, Fang] Zhejiang Cady Ind Co Ltd, Huzhou 313013, Peoples R China; [Yang, Guang; Hua, Zan] Anhui Agr Univ, Biomass Mol Engn Ctr, Dept Mat Sci & Engn, Hefei 230036, Peoples R China published TEMPO-Functionalized Nanoreactors from Bottlebrush Copolymers for the Selective Oxidation of Alcohols in Water in 2021, Cited 56. Computed Properties of C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Polymeric nanoreactors in water fabricated by the self-assembly of amphiphilic copolymers have attracted much attention due to their good catalytic performance without using organic solvents. However, the disassembly and instability of relevant nanostructures often compromise their potential applicability. Herein, the preparation of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-containing nanoreactors by the self-assembly of amphiphilic bottle-brush copolymers has been demonstrated. First, a macromonomer having a norbornenyl polymerizable group was prepared by RAFT polymerization of hydrophobic and hydrophilic monomers. The macromonomer was further subjected to ring-opening metathesis polymerization to produce an amphiphilic bottlebrush copolymer. Further, TEMPO, as a catalyst, was introduced into the hydrophobic block through the activated ester strategy. Finally, TEMPO-functionalized polymeric nanoreactors were successfully obtained by self-assembly in water. The nanoreactors exhibited excellent catalytic activities in selective oxidation of alcohols in water. More importantly, the reaction kinetics showed that the turnover frequency is greatly increased compared to that of the similar nanoreactor prepared from liner copolymers under the same conditions. The outstanding catalytic activities of the nanoreactors from bottlebrush copolymers could be attributed to the more stable micellar structure using the substrate concentration effect. This work presents a new strategy to fabricate stable nanoreactors, paving the way for highly efficient organic reactions in aqueous solutions.

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Authors Yamamoto, Y; Ota, M; Kodama, S; Michimoto, K; Nomoto, A; Ogawa, A; Furuya, M; Kawakami, K in AMER CHEMICAL SOC published article about in [Yamamoto, Yuki; Ota, Miyuto; Kodama, Shintaro; Michimoto, Kazuki; Nomoto, Akihiro; Ogawa, Akiya] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Sakai, Osaka 5998531, Japan; [Furuya, Mitsunori; Kawakami, Kiminori] Mitsubishi Chem Corp, Sci & Innovat Ctr, Yokohama, Kanagawa 2278502, Japan in 2021, Cited 67. Recommanded Product: (4-Methoxyphenyl)methanol. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A green method for the oxidation of alcohols to carboxylic acids was developed using a novel co-catalytic system based on gold, silver, and copper catalysts. This reaction system was conducted under atmospheric oxygen in water and mild conditions to selectively oxidize 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid, as a building block for polyethylene furanoate, which is a 100% bio-based, future alternative to the petroleum-based polyethylene terephthalate. Furthermore, various primary alcohols were conveniently oxidized to their corresponding carboxylic acids in up to quantitative yields.

Recommanded Product: (4-Methoxyphenyl)methanol. Welcome to talk about 105-13-5, If you have any questions, you can contact Yamamoto, Y; Ota, M; Kodama, S; Michimoto, K; Nomoto, A; Ogawa, A; Furuya, M; Kawakami, K or send Email.

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Application In Synthesis of (4-Methoxyphenyl)methanol. I found the field of Engineering very interesting. Saw the article Photoactive amphiphilic nanoreactor: A chloroplast-like catalyst for natural oxidation of alcohols published in 2021, Reprint Addresses Shi, ZQ (corresponding author), Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Coll Chem, Changchun 130012, Peoples R China.. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol.

Exploring catalytic processes performed under natural conditions is interesting, but there remains a great challenge in developing highly efficient catalysts for natural oxidation of alcohols. Herein, we report a chloroplast-like catalyst comprised of photoactive carbon dots (CDs), catalytically active Pt nanoparticles, and amphiphilic nanotubes. Under simulated and real natural reaction conditions, our catalysts exhibited remarkable activity and long-term reusability for the oxidation of various alcohols, significantly outperforming that of other counterpart catalysts and reported thermal/photocatalytic systems. It was demonstrated that when the carbon dots and the amphiphilic nanotubes respectively played a role in the light-harvesting and the substrate transport the Pt/CDs heterointerface acted as the active center for the matter conversion. Such an elaborate cooperation, an advanced process in the photosynthesis of plant, contributed to the excellent catalytic performance. This contribution provides a new design concept for artificial photocatalysts, which is very promising for developing sustainable catalytic processes.

Welcome to talk about 105-13-5, If you have any questions, you can contact Shi, ZQ; Qu, XJ; Dai, JY; Zou, HB; Zhang, ZT; Wang, RW; Qiu, SL or send Email.. Application In Synthesis of (4-Methoxyphenyl)methanol

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An article Preparation and evaluation a mixed-mode stationary phase with C-18 and 2-methylindole for HPLC WOS:000608700300001 published article about PERFORMANCE LIQUID-CHROMATOGRAPHY in [Hosseini, Elham Sadat; Tabar Heydar, Kourosh] Chem & Chem Engn Res Ctr Iran, Fac Clean Technol, Tehran, Iran in 2021, Cited 42. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Product Details of 105-13-5

A modified C-18 column (Silpr-2MI-C18) was prepared using 2-methylindole and C-18 reagent. The extent of C-18 hydrocarbon chain, conjugative rings and anion exchange site provided multiple retention mechanisms, including reversed-phase liquid chromatography (RPLC), pi-pi interaction, hydrophilic interaction liquid chromatography (HILIC) and anion exchange chromatography (AEC). The separation of protected amino acids was investigated on the commercial C-18 and Silpr-2MI-C18 columns, while the chromatographic conditions, including methanol content and pH of the mobile phase, were studied. The separation arrangement of the hydrophilic amino acids was different on the Silpr-2MI-C18 column compared to the commercial C-18 column under RPLC mode. Furthermore, these amino acids were separated on the Silpr-2MI-C18 column under HILIC mode. The modified C-18 column was employed to separate amino acids, alkylbenzenes and polycyclic aromatic hydrocarbons under RPLC mode and inorganic anion under AEC mode. The results confirm that this new stationary phase of RPLC/HILIC/AEC has multiple interactions with different analytes. Effective retention of biological samples was found on the Silpr-2MI-C18 column by comparing the results obtained from the commercial C-18 column.

Welcome to talk about 105-13-5, If you have any questions, you can contact Hosseini, ES; Heydar, KT or send Email.. Product Details of 105-13-5

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