Month: October 2021

Shahriari, M; Sedigh, MA; Mahdavian, Y; Mahdigholizad, S; Pirhayati, M; Karmakar, B; Veisi, H in [Shahriari, Marjan] Islamic Azad Univ, Fac Pharmaceut Chem, Dept Pharmaceut Chem, Tehran Med Sci, Tehran, Iran; [Sedigh, Mohammad Alihosseini] Islamic Azad Univ, Fac Pharmaceut Chem, Dept Organ Chem, Tehran Med Sci, Tehran, Iran; [Mahdavian, Yasamin] Islamic Azad Univ, Fac Pharmaceut Chem, Dept Appl Chem, Tehran Med Sci, Tehran, Iran; [Mahdigholizad, Siavash] Iran Univ Med Sci, Sch Med, Tehran, Iran; [Pirhayati, Mozhgan] Malayer Univ, Fac Sci, Dept Appl Chem, Malayer, Iran; [Karmakar, Bikash] Gobardanga Hindu Coll, Dept Chem, Gobardanga, India; [Veisi, Hojat] Payame Noor Univ, Dept Chem, Tehran, Iran published In situ supported Pd NPs on biodegradable chitosan/agarose modified magnetic nanoparticles as an effective catalyst for the ultrasound assisted oxidation of alcohols and activities against human breast cancer in 2021, Cited 57. Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

In this content, a green approach for the ultrasound promoted in situ immobilization of Pd NPs over biodegradable chitosan/agarose modified ferrite NP (Fe3O4@CS-Agarose/Pd) is developed. The structural and physicochemical features of the material were estimated using advanced analytical techniques like FT-IR, ICP-OES, FESEM, EDS, XRD, TEM and VSM. The magnetic material was catalytically explored in the oxidation of alcohols under ultrasonic waves. Sonication had a significant role in enhancing the catalytic performance in the alcohol’s oxidation as compared to conventional heating. The heterogeneous nanocatalyst was efficiently recycled up to 10 times with nominal loss in catalytic activity. Towards the biological applications, the Fe3O4@CS-Agarose/Pd nanocomposite showed high antioxidant activities against DPPH free radicals, comparable to standard butylated hydroxytoluene (BHT). In addition, it exhibited excellent cytotoxicity in terms of % cell viability against breast adenocarcinoma (MCF7), breast carcinoma (Hs 578Bst), infiltrating ductal cell carcinoma (Hs 319.T), and metastatic carcinoma (MDA-MB-453) cell lines. The best anti-breast cancer potential of the nanocomposite was observed in Hs 319.T cell line. (C) 2021 Published by Elsevier B.V.

Formula: C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Shahriari, M; Sedigh, MA; Mahdavian, Y; Mahdigholizad, S; Pirhayati, M; Karmakar, B; Veisi, H or concate me.

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Recommanded Product: (4-Methoxyphenyl)methanol. In 2021 ASIAN J ORG CHEM published article about CARBOXYLIC-ACID SALTS; SECONDARY ALCOHOLS; DEHYDROGENATIVE OXIDATION; DIRECT FUNCTIONALIZATION; CROSS-COUPLINGS; COMPLEX BEARING; N-ALKYLATION; PPM LEVELS; WATER; COBALT in [Verma, Ashutosh; Hazra, Susanta; Dolui, Pritam; Elias, Anil J.] Indian Inst Technol, Dept Chem, New Delhi 110016, India in 2021, Cited 118. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Herein, we report a simple, efficient, and sustainable method for the synthesis of alpha-alkylated ketones and quinolines using a hydrogen-borrowing strategy, which has emerged as a greener alternative in organic transformation reactions. Synthesis of a range of alpha-alkylated ketones and quinoline derivatives was achieved by using the water-soluble [Ru(8-AQ)Cl(p-cym.)]Cl-+(-) [Ru]-1 (AQ=aminoquinoline) catalyst with water as the reaction medium. By adopting this strategy, we have synthesized alpha-alkylated ketones and quinolines using ketones or secondary alcohols as starting materials and the primary alcohol as a green and naturally abundant alkylating agent.

Recommanded Product: (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Verma, A; Hazra, S; Dolui, P; Elias, AJ or concate me.

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An article Direct Heterogenization of the Ru-Macho Catalyst for the Chemoselective Hydrogenation of alpha,beta-Unsaturated Carbonyl Compounds WOS:000653539100005 published article about RUTHENIUM PINCER COMPLEX; POROUS ORGANIC POLYMER; SELECTIVE HYDROGENATION; HOMOGENEOUS HYDROGENATION; UNSATURATED ALDEHYDES; CYCLIC CARBONATES; ACTIVATED CARBON; SCALE SYNTHESIS; EFFICIENT; METHANOL in [Padmanaban, Sudakar; Yoon, Sungho] Chung Ang Univ, Dept Chem, Seoul 06974, South Korea; [Padmanaban, Sudakar] Seoul Natl Univ, Dept Chem, Seoul 08826, South Korea; [Gunasekar, Gunniya Hariyanandam] Korea Inst Sci & Technol, Clean Energy Res Ctr, Seoul 136791, South Korea in 2021, Cited 95. COA of Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

In this study, a commercially available homogeneous pincer-type complex, Ru-Macho, was directly heterogenized via the Lewis acid-catalyzed Friedel-Crafts reaction using dichloromethane as the cross-linker to obtain a heterogeneous, pincer-type Ru porous organometallic polymer (Ru-Macho-POMP) with a high surface area. Notably, Ru-Macho-POMP was demonstrated to be an efficient heterogeneous catalyst for the chemoselective hydrogenation of alpha,beta-unsaturated carbonyl compounds to their corresponding allylic alcohols using cinnamaldehyde as a model compound. The Ru-Macho-POMP catalyst showed a high turnover frequency (TOF = 920 h(-1)) and a high turnover number (TON = 2750), with high chemoselectivity (99%) and recyclability during the selective hydrogenation of alpha, beta-unsaturated carbonyl compounds.

COA of Formula: C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Padmanaban, S; Gunasekar, GH; Yoon, S or concate me.

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In 2021 SYNTHESIS-STUTTGART 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.

Category: alcohols-buliding-blocks. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Inatomi, S; Takayanagi, Y; Watanabe, K; Toita, A; Yamakoshi, H; Nakamura, S or concate me.

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Application In Synthesis of (4-Methoxyphenyl)methanol. Authors Luo, NH; Zhong, YH; Wen, HL; Shui, HL; Luo, RS in WILEY-V C H VERLAG GMBH published article about in [Luo, Nianhua; Zhong, Yuhong; Wen, Huiling; Shui, Hongling; Luo, Renshi] Gannan Med Univ, Sch Pharmaceut Sci, Ganzhou 341000, Jiangxi, Peoples R China in 2021, Cited 94. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Ketones are of great importance in synthesis, biology, and pharmaceuticals. This paper reports an iridium complexes-catalyzed cross-coupling of alcohols via hydrogen borrowing, affording a series of alpha-alkylated ketones in high yield (86 %-95 %) and chemoselectivities (>99 : 1). This methodology has the advantages of low catalyst loading (0.1 mol%) and environmentally benign water as the solvent. Studies have shown the amount of base has a great impact on chemoselectivities. Meanwhile, deuteration experiments show water plays an important role in accelerating the reduction of the unsaturated ketones intermediates. Remarkably, a gram-scale experiment demonstrates this methodology of iridium-catalyzed cross-coupling of alcohols has potential application in the practical synthesis of alpha-alkylated ketones.

Application In Synthesis of (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Luo, NH; Zhong, YH; Wen, HL; Shui, HL; Luo, RS or concate me.

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I found the field of Chemistry very interesting. Saw the article Dioxido-vanadium(V) complex catalyzed oxidation of alcohols and tandem synthesis of oximes: a simple catalytic protocol for C-N bond formation published in 2021. Formula: C8H10O2, Reprint Addresses Kurbah, SD (corresponding author), Pandit Deendayal Upadhyaya Adarsha Mahavidyalaya, Dept Chem, Eraligool 788723, Assam, India.. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol

We report the synthesis of a vanadium(V) complex characterized by FT-IR and H-1 NMR spectroscopy. The structure of the complex was established by single crystal X-ray crystallography. We also carried out the catalytic oxidation of benzyl alcohol, hetero-aryl alcohols and propargylic alcohols. Tandem synthesis of oximes from alcohols were also carried out using our vanadium(V) complex. The newly synthesized complex acts as a catalyst for oxidation reactions and tandem synthesis of oxime from alcohols. [GRAPHICS] .

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Kurbah, SD or concate me.. Formula: C8H10O2

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Application In Synthesis of (4-Methoxyphenyl)methanol. Hosseini, ES; Heydar, KT in [Hosseini, Elham Sadat; Tabar Heydar, Kourosh] Chem & Chem Engn Res Ctr Iran, Fac Clean Technol, Tehran, Iran published Preparation and evaluation a mixed-mode stationary phase with C-18 and 2-methylindole for HPLC in 2021, Cited 42. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery 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.

Application In Synthesis of (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Hosseini, ES; Heydar, KT or concate me.

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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. Safety of (4-Methoxyphenyl)methanol. 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.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Wang, ML; Xu, ZK; Shi, Y; Cai, F; Qiu, JQ; Yang, G; Hua, Z; Chen, T or concate me.. Safety of (4-Methoxyphenyl)methanol

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Authors Jin, B; Wang, JG; Xu, FX; Li, DF; Men, Y in ELSEVIER published article about in [Jin, Bei; Wang, Jinguo; Xu, Fengxia; Li, Dianfeng; Men, Yong] Shanghai Univ Engn Sci, Sch Chem & Chem Engn, Shanghai 201620, Peoples R China in 2021, Cited 59. COA of Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Selective conversion of biomass-derived alcohols into carbonyl compounds via visible-light photocatalysis is realized over hierarchical hollow WO3 microspheres with tailored surface oxygen vacancies, which presents the remarkably boosted photoactivity in terms of selectivity and activity, intrinsically attributing to the strong synergetic effect of hierarchical spherical cavity and surface oxygen vacancies simultaneously. The hierarchical spherical cavity, substantially constructed by the self-interconnected nanosheets, enhances the light-harvesting ability via multiple light reflections not only in spherical cavity but also among the self-interconnected nanosheets. Surface oxygen vacancies favor the energy band gap narrowing via forming a miniband just below the conduction band and then extend the photoresponse region, further boosting the light-harvesting ability. Importantly, surface oxygen vacancies function as the electron sinks to capture photoelectrons and thus restrict their recombination probability with holes, finally improving the photoelectron-hole separation efficiency. Meanwhile, this photocatalyst presents excellent reusability, showing its promising potential in practical applications. This work sheds light on a new application of hierarchical WO3 microspheres with tailored surface oxygen vacancies and its strong synergetic effect of hierarchical structures and surface oxygen vacancies on photocatalytic performance, delivering new insights for rationally designing highly active photocatalysts applied in future green and sustainable organic transformation reactions.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Jin, B; Wang, JG; Xu, FX; Li, DF; Men, Y or concate me.. COA of Formula: C8H10O2

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Name: (4-Methoxyphenyl)methanol. Authors Uygur, M; Kuhlmann, JH; Perez-Aguilar, MC; Piekarski, DG; Mancheno, OG in ROYAL SOC CHEMISTRY published article about in [Uygur, Mustafa; Kuhlmann, Jan H.; Perez-Aguilar, Maria Carmen; Piekarski, Dariusz G.; Mancheno, Olga Garcia] Westfalische Wilhelms Univ Munster, Organ Chem Inst, Correnstr 36, D-48149 Munster, Germany; [Piekarski, Dariusz G.] Polish Acad Sci, Inst Phys Chem, Kasprzaka 44-52, PL-01224 Warsaw, Poland in 2021, Cited 80. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A metal- and additive-free methodology for the highly selective, photocatalyzed C-H oxygenation of alkylarenes under air to the corresponding carbonyls is presented. The process is catalyzed by an imide-acridinium that forms an extremely strong photooxidant upon visible light irradiation, which is able to activate inert alkylarenes such as toluene. Hence, this is an easy to perform, sustainable and environmentally friendly oxidation that provides valuable carbonyls from abundant, readily available compounds.

Name: (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Uygur, M; Kuhlmann, JH; Perez-Aguilar, MC; Piekarski, DG; Mancheno, OG or concate me.

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