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Product Details of 105-13-5. Authors Pandey, VK; Tiwari, CS; Rit, A in AMER CHEMICAL SOC published article about in [Pandey, Vipin K.; Tiwari, Chandra Shekhar; Rit, Arnab] Indian Inst Technol Madras, Dept Chem, Chennai 600036, Tamil Nadu, India in 2021, Cited 56. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

AgSbF6 was developed as an effective catalyst for the hydroboration of various unsaturated functionalities (nitriles, alkenes, and aldehydes). This atom-economic chemoselective protocol works effectively under low catalyst loading, base- and solvent-free moderate conditions. Importantly, this process shows excellent functional group tolerance and compatibility with structurally and electronically diverse substrates (>50 examples). Mechanistic investigations revealed that the reaction proceeds via a radical pathway. Further, the obtained N,N-diborylamines were showcased to be useful precursors for amide synthesis.

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Recommanded Product: (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.

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Authors Bolen, SD; Love, TE; Einstadter, D; Lever, J; Lewis, S; Persaud, H; Fiegl, J; Liu, RJ; Ali-Matlock, W; Bar-Shain, D; Caron, A; Misak, J; Wagner, T; Kauffman, E; Cook, L; Hebert, C; White, S; Kobaivanova, N; Cebul, R in SPRINGER published article about in [Bolen, Shari D.; Love, Thomas E.; Einstadter, Douglas; Lewis, Steven; Bar-Shain, David; Caron, Aleece; Cebul, Randall] Case Western Reserve Univ, Populat Hlth Res Inst, Ctr Hlth Care Res & Policy, MetroHlth Syst, Cleveland, OH 44106 USA; [Bolen, Shari D.; Love, Thomas E.; Einstadter, Douglas; Lever, Jonathan; Ali-Matlock, Wanda; Bar-Shain, David; Cebul, Randall] Better Hlth Partnership, Cleveland, OH USA; [Bolen, Shari D.; Love, Thomas E.; Einstadter, Douglas; Lewis, Steven; Caron, Aleece] Case Western Reserve Univ, Dept Med, MetroHlth Syst, Cleveland, OH 44106 USA; [Bolen, Shari D.; Love, Thomas E.; Einstadter, Douglas; Persaud, Harry; Cebul, Randall] Case Western Reserve Univ, Dept Populat & Quantitat Hlth Sci, Cleveland, OH 44106 USA; [Fiegl, Jordan] Univ Hosp, Dept Data Sci & Analyt, Cleveland, OH USA; [Liu, Rujia] Medpace Inc, Cincinnati, OH USA; [Bar-Shain, David] Case Western Reserve Univ, Dept Pediat, Cleveland, OH 44106 USA; [Misak, James] Case Western Reserve Univ, Dept Family Med, MetroHlth Syst, Cleveland, OH 44106 USA; [Wagner, Todd] Signature Hlth, Mentor, OH USA; [Kauffman, Erick] Neighborhood Family Practice, Cleveland, OH USA; [Cook, Lloyd] Med Mutual, Cleveland, OH USA; [Hebert, Christopher] Mercy Hlth, Cincinnati, OH USA; [Kobaivanova, Nana] Cleveland Clin, Cleveland, OH USA in 2021, Cited 28. Computed Properties of C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

BACKGROUND: Accelerated translation of real-world interventions for hypertension management is critical to improving cardiovascular outcomes and reducing disparities. OBJECTIVE: To determine whether a positive deviance approach would improve blood pressure (BP) control across diverse health systems. DESIGN: Quality improvement study using 1-year cross sections of electronic health record data over 5 years (2013-2017). PARTICIPANTS: Adults >= 18 with hypertension with two visits in 2 years with at least one primary care visit in the last year (N = 114,950 at baseline) to a primary care practice in Better Health Partnership, a regional health improvement collaborative. INTERVENTIONS: Identification of a positive deviant and dissemination of this system’s best practices for control of hypertension (i.e., accurate/repeat BP measurement; timely follow-up; outreach; standard treatment algorithm; and communication curriculum) using 3 different intensities (low: Learning Collaborative events describing the best practices; moderate: Learning Collaborative events plus consultation when requested; and high: Learning Collaborative events plus practice coaching). MAIN MEASURES: We used a weighted linear model to estimate the pre- to post-intervention average change in BP control (< 140/90 mmHg) for 35 continuously participating clinics. KEY RESULTS: BP control post-intervention improved by 7.6% [95% confidence interval (CI) 6.0-9.1], from 67% in 2013 to 74% in 2017. Subgroups with the greatest absolute improvement in BP control included Medicaid (12.0%, CI 10.5-13.5), Hispanic (10.5%, 95% CI 8.4-12.5), and African American (9.0%, 95% CI 7.7-10.4). Implementation intensity was associated with improvement in BP control (high: 14.9%, 95% CI 0.2-19.5; moderate: 5.2%, 95% CI 0.8-9.5; low: 0.2%, 95% CI-3.9 to 4.3). CONCLUSIONS: Employing a positive deviance approach can accelerate translation of real-world best practices into care across diverse health systems in the context of a regional health improvement collaborative (RHIC). Using this approach within RHICs nationwide could translate to meaningful improvements in cardiovascular morbidity and mortality. Computed Properties of C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Bolen, SD; Love, TE; Einstadter, D; Lever, J; Lewis, S; Persaud, H; Fiegl, J; Liu, RJ; Ali-Matlock, W; Bar-Shain, D; Caron, A; Misak, J; Wagner, T; Kauffman, E; Cook, L; Hebert, C; White, S; Kobaivanova, N; Cebul, R or send Email.

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In 2021 CATAL SCI TECHNOL published article about GAS SHIFT REACTION; PRIMARY AMINES; NUCLEOPHILIC ALLYLATION; MOLECULAR COMPLEXITY; ALDEHYDES; RUTHENIUM; HYDROGEN; KETONES; CL; NITROARENES in [Biriukov, Klim O.; Vinogradov, Mikhail M.; Afanasyev, Oleg, I; Tsygankov, Alexey A.; Godovikova, Maria; Nelyubina, Yulia, V; Loginov, Dmitry A.; Chusov, Denis] Russian Acad Sci INEOS RAS, AN Nesmeyanov Inst Organoelement Cpds, Vavilova St 28, Moscow, Russia; [Vasilyev, Dmitry V.] Forschungszentrum Julich, Helmholtz Inst Erlangen Nurnberg Renewable Energy, Egerlandstr 3, D-91058 Erlangen, Germany; [Loginov, Dmitry A.; Chusov, Denis] GV Plekhanov Russian Univ Econ, 36 Stremyanny Per, Moscow 117997, Russia in 2021, Cited 71. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Category: alcohols-buliding-blocks

Herein, we present the first example of Os-catalyzed efficient reductive amination under water-gas shift reaction conditions. The developed catalytic systems are formed in situ in aqueous solutions, employ as small as 0.0625 mol% osmium and are capable of delivering reductive amination products for a broad range of aliphatic and aromatic carbonyl compounds and amines. The scope of the reaction, active catalytic systems, possible limitations of the method and DFT-supported mechanistic considerations are discussed in detail in the manuscript.

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Category: alcohols-buliding-blocks. Authors Bains, AK; Yadav, A; Adhikari, D in AMER CHEMICAL SOC published article about in [Bains, Amreen K.; Adhikari, Debashis] Indian Inst Sci Educ & Res IISER Mohali, Dept Chem Sci, Ajitgarh 140306, Punjab, India; [Yadav, Ankit] Indian Inst Sci Educ & Res IISER Mohali, Dept Earth & Environm Sci, Ajitgarh 140306, Punjab, India in 2021, Cited 35. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Herein, we report a combination of pyrenedione (PD) and KO’Bu to achieve facile alcohol dehydrogenation under visible-light excitation, where aerobic oxygen is utilized as the terminal oxidant. The resulting carbonyl compound can be easily converted to vinyl nitriles in a single-pot reaction, at 60 degrees C in 6-8 h. This environmentally benign, organocatalytic approach has distinct advantages over transition-metal-catalyzed a-olefination of nitriles, which often operate at a significantly higher temperature for an extended reaction time.

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Formula: C8H10O2. Recently I am researching about ALPHA-ALKYLATION; N-ALKYLATION; EFFICIENT CATALYSTS; BORROWING HYDROGEN; PINCER COMPLEXES; AROMATIC-AMINES; MANGANESE; KETONES; METHYLATION; IMINES, Saw an article supported by the National Science FoundationNational Science Foundation (NSF) [CHE-1465051, MRI CHE-1626549]; URECA; Clean Energy Fee Funds of MTSU; FRCAC. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Pandey, B; Xu, S; Ding, KY. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol

beta-alkylation of secondary alcohols with primary alcohols to selectively generate alcohols by a well-defined Co catalyst is presented. Remarkably, a low catalyst loading of 0.7 mol % can be employed for the reaction. More significantly, this study represents the first Co-catalyzed switchable alcohol/ketone synthesis by simply manipulating the reaction parameters. In addition, the transformation is environmentally friendly, with water as the only byproduct.

Formula: C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Pandey, B; Xu, S; Ding, KY or send Email.

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Name: (4-Methoxyphenyl)methanol. Authors Aydin, BO; Anil, D; Demir, Y in WILEY-V C H VERLAG GMBH published article about in [Aydin, Busra O.; Anil, Derya] Ataturk Univ, Dept Chem, Fac Sci, Erzurum, Turkey; [Anil, Derya] Ataturk Univ, Tech Sci Vocat Sch, Dept Chem & Chem Proc Technol, Erzurum, Turkey; [Demir, Yeliz] Ardahan Univ, Nihat Delibalta Gole Vocat Sch, Dept Pharm Serv, Ardahan, Turkey in 2021, Cited 53. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Fused pyrimidines, especially pyrazolo[3,4-d]pyrimidines, are among the most preferred building blocks for pharmacology studies, as they exhibit a broad spectrum of biological activity. In this study, new derivatives of pyrazolo[3,4-d]pyrimidine were synthesized by alkylation of the N1 nitrogen atom. We synthesized 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine 2 from commercially available aminopyrazolopyrimidine 1 using N-iodosuccinimide as an iodinating agent. The synthesis of compound 2 started with nucleophilic substitution of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine with R-X (X: -OMs, -Br, -Cl), affording N-alkylated pyrazolo[3,4-d]pyrimidine. We performed this synthesis using a weak inorganic base and the mild temperature was also used for a two-step procedure to generate N-alkylated pyrazolo[3,4-d]pyrimidine derivatives. Also, all compounds were tested for their ability to inhibit acetylcholinesterase (AChE) and the human carbonic anhydrase (hCA) isoforms I and II, with K-i values in the range of 15.41 +/- 1.39-63.03 +/- 10.68 nM for AChE, 17.68 +/- 1.92-66.27 +/- 5.43 nM for hCA I, and 8.41 +/- 2.03-28.60 +/- 7.32 nM for hCA II. Notably, compound 10 was the most selective and potent CA I inhibitor with a significant selectivity ratio of 26.90.

Name: (4-Methoxyphenyl)methanol. Welcome to talk about 105-13-5, If you have any questions, you can contact Aydin, BO; Anil, D; Demir, Y or send Email.

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An article Bioinspired Radical-Mediated Transition-Metal-Free Synthesis of N-Heterocycles under Visible Light WOS:000590308900001 published article about DEPENDENT AMINE OXIDASES; AEROBIC OXIDATION; CATALYTIC MECHANISM; ALCOHOL OXIDATION; TOPA QUINONE; ACTIVE-SITE; COPPER; HYDROGEN; MODEL; PYRIMIDINES in [K. Bains, Amreen; Adhikari, Debashis] Indian Inst Sci Educ & Res IISER Mohali, Dept Chem Sci, Sas Nagar 140306, Punjab, India; [Ankit, Yadav] Indian Inst Sci Educ & Res IISER Mohali, Dept Earth & Environm Sci, Sas Nagar 140306, Punjab, India in 2021, Cited 42. Quality Control of (4-Methoxyphenyl)methanol. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A redox-active iminoquinone motif connected with pi-delocalized pyrene core has been reported that can perform efficient two-electron oxidation of a class of substrates. The design of the molecule was inspired by the organic redox cofactor topaquinone (TPQ), which executes amine oxidation in the enzyme, copper amine oxidase. Easy oxidation of both primary and secondary alcohols happened in the presence of catalytic KOtBu, which could reduce the ligand backbone to its iminosemiquinonate form under photoinduced conditions. Moreover, this easy oxidation of alcohols under aerobic condition could be elegantly extended to multi-component, one-pot coupling for the synthesis of quinoline and pyrimidine. This organocatalytic approach is very mild (70 degrees C, 8 h) compared to a multitude of transition-metal catalysts that have been used to prepare these heterocycles. A detailed mechanistic study proves the intermediacy of the iminosemiquinonate-type radical and a critical hydrogen atom transfer step to be involved in the dehydrogenation reaction.

Quality Control of (4-Methoxyphenyl)methanol. Welcome to talk about 105-13-5, If you have any questions, you can contact Bains, AK; Ankit, Y; Adhikari, D or send Email.

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Name: (4-Methoxyphenyl)methanol. Arslan, B; Gulcemal, S in [Arslan, Burcu; Gulcemal, Suleyman] Ege Univ, Dept Chem, TR-35100 Izmir, Turkey published alpha-Alkylation of arylacetonitriles with primary alcohols catalyzed by backbone modified N-heterocyclic carbene iridium(I) complexes in 2021, Cited 65. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

A series of backbone-modified N-heterocyclic carbene (NHC) complexes of iridium(I) (1d-f) have been synthesized and characterized. The electronic properties of the NHC ligands have been assessed by comparison of the IR carbonyl stretching frequencies of the in situ prepared [IrCl(CO)(2)(NHC)] complexes in CH2Cl2. These new complexes (1d-f), together with previously prepared 1a-c, were applied as catalysts for the alpha-alkylation of arylacetonitriles with an equimolar amount of primary alcohols or 2-aminobenzyl alcohol. The catalytic activities of these complexes could be controlled by modifying the N-substituents and backbone of the NHC ligands. The NHC-Ir-I complex 1f bearing 4-methoxybenzyl substituents on the N-atoms and 4-methoxyphenyl groups at the 4,5-positions of imidazole exhibited the highest catalytic activity in the alpha-alkylation of arylacetonitriles with primary alcohols. Various alpha-alkylated nitriles and aminoquinolines were obtained in high yields through a borrowing hydrogen pathway by using 0.1 mol% 1f and a catalytic amount of KOH (5 mol%) under an air atmosphere within significantly short reaction times.

Name: (4-Methoxyphenyl)methanol. Welcome to talk about 105-13-5, If you have any questions, you can contact Arslan, B; Gulcemal, S or send Email.

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Recently I am researching about FACILE SYNTHESIS; REACTANTS ACTIVATION; NO ADSORPTION; DOPED G-C3N4; EFFICIENT; NANOSHEETS; ZIRCONIA; REACTIVITY; VACANCIES; MECHANISM, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21501016, 21822601, 21777011]; Innovative Research Team of Chongqing [CXTDG201602014, CXQT19023]; Natural Science Foundation of ChongqingNatural Science Foundation of Chongqing [cstc2017jcyjBX0052]; Plan for National Youth Talents of the Organization Department of the Central Committee. Safety of (4-Methoxyphenyl)methanol. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Wang, JD; Cui, W; Chen, RM; He, Y; Yuan, CW; Sheng, JP; Li, JY; Zhan, YX; Dong, F; Sun, YJ. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (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.

About (4-Methoxyphenyl)methanol, 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 concate me.. Safety of (4-Methoxyphenyl)methanol

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