Tag: M.W=100-150

Babu, R; Subaramanian, M; Midya, SP; Balaraman, E in [Babu, Reshma; Subaramanian, Murugan; Midya, Siba P.; Balaraman, Ekambaram] Indian Inst Sci Educ & Res IISER Tirupati, Dept Chem, Tirupati 517507, Andhra Pradesh, India published Nickel-Catalyzed Guerbet Type Reaction: C-Alkylation of Secondary Alcohols via Double (de)Hydrogenation in 2021, Cited 56. Product Details of 105-13-5. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Acceptorless double dehydrogenative cross-coupling of secondary and primary alcohols under nickel catalysis is reported. This Guerbet type reaction provides an atom- and a step-economical method for the C-alkylation of secondary alcohols under mild, benign conditions. A broad range of substrates including aromatic, cyclic, acyclic, and aliphatic alcohols was well tolerated. Interestingly, the C-alkylation of cholesterol derivatives and the double C-alkylation of cyclopentanol with various alcohols were also demonstrated.

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An article Engineered Superparamagnetic Core-Shell Metal-Organic Frame-Work (Fe3O4@Ni-Co-BTC NPs) with Enhanced Photocatalytic Activity for Selective Aerobic Oxidation of Alcohols Under Solar Light Irradiation WOS:000543030400002 published article about BENZYL ALCOHOL; EFFICIENT CATALYST; AROMATIC ALCOHOLS; GRAPHENE OXIDE; NANOPARTICLES; PERFORMANCE; WATER; OXYGEN; BI2WO6; MOF in [Mohammadinezhad, Arezou; Akhlaghinia, Batool] Ferdowsi Univ Mashhad, Fac Sci, Dept Chem, Mashhad 9177948974, Razavi Khorasan, Iran in 2021, Cited 70. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Recommanded Product: (4-Methoxyphenyl)methanol

This paper reported an environmentally benign strategy for the synthesis of a magnetic metal-organic framework (Fe3O4@Ni-Co-BTCNPs) via a multi-step procedure. The catalytic performance of Fe3O4@Ni-Co-BTCNPs was evaluated in the selective aerobic oxidation of alcohol substrates (including primary and secondary aliphatic and benzylic alcohols) in water and under solar light irradiation. [GRAPHICS] .

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Amberchan, G; Snelling, RA; Moya, E; Landi, M; Lutz, K; Gatihi, R; Singaram, B in [Amberchan, Gabriella; Snelling, Rachel A.; Moya, Enrique; Landi, Madison; Lutz, Kyle; Gatihi, Roxanne; Singaram, Bakthan] Univ Calif Santa Cruz, Dept Chem & Biochem, Santa Cruz, CA 95064 USA published Reaction of Diisobutylaluminum Borohydride, a Binary Hydride, with Selected Organic Compounds Containing Representative Functional Groups in 2021, Cited 84. Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

The binary hydride, diisobutylaluminum borohydride [(iBu)(2)AlBH4], synthesized from diisobutylaluminum hydride (DIBAL) and borane dimethyl sulfide (BMS) has shown great potential in reducing a variety of organic functional groups. This unique binary hydride, (iBu)(2)AlBH4, is readily synthesized, versatile, and simple to use. Aldehydes, ketones, esters, and epoxides are reduced very fast to the corresponding alcohols in essentially quantitative yields. This binary hydride can reduce tertiary amides rapidly to the corresponding amines at 25 degrees C in an efficient manner. Furthermore, nitriles are converted into the corresponding amines in essentially quantitative yields. These reactions occur under ambient conditions and are completed in an hour or less. The reduction products are isolated through a simple acid-base extraction and without the use of column chromatography. Further investigation showed that (iBu)(2)AlBH4 has potential to be a selective hydride donor as shown through a series of competitive reactions. Similarities and differences between (iBu)(2)AlBH4, DIBAL, and BMS are discussed.

Formula: C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Amberchan, G; Snelling, RA; Moya, E; Landi, M; Lutz, K; Gatihi, R; Singaram, B or send Email.

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Authors Agarwal, S; Phukan, P; Sarma, D; Deori, K in ROYAL SOC CHEMISTRY published article about BENZYL ALCOHOL; DYE DEGRADATION; CUS; EFFICIENT; EVOLUTION; TIO2; 1,2,3-TRIAZOLES; MICROSPHERES; NANOCRYSTALS; REDUCTION in [Agarwal, Soniya; Phukan, Parmita; Sarma, Diganta; Deori, Kalyanjyoti] Dibrugarh Univ, Dept Chem, Dibrugarh 786004, Assam, India in 2021, Cited 49. Category: alcohols-buliding-blocks. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A series of copper sulfide (CS) nanoparticles (NPs) were synthesized just by varying the amount of the sulfur precursor and have been explored for the first time as a three-way heterogeneous catalyst in the photocatalytic oxidation of a number of aromatic alcohols, photocatalytic degradation and the reduction of water pollutants, and the facile synthesis of pharmaceutically important moiety 4-aryl-NH-1,2,3-triazoles. The green and novel protocol was successfully developed for the synthesis of covellite (CuS, Cu2+) and the covellite-villamaninite (CuS-CuS2) (copper in Cu2+, Cu1+) phases of copper sulfide, employing EDTA both as the chelating and capping agent via a simple precipitation method at room temperature using water as the solvent. A blue shift in the absorption spectra and band gap in the range of 2.02-2.07 eV prompted the investigation of the as-synthesized CS nanoparticles as the photocatalyst under visible light irradiation. In the absence of any oxidizing or reducing agent, covellite CuS nanoparticles showed the highest photocatalytic efficiency for the degradation of methylene blue (MB) and the reduction of carcinogenic and mutagenic Cr(vi) to non-toxic Cr(iii). Interestingly, the mixed phase of CS (CuS-CuS2), where Cu is present in both +1 and +2 oxidation states, was found to be the most efficient catalyst compared to CuS toward the visible light-mediated selective oxidation of various benzyl alcohols to their corresponding aldehydes. However, in the synthesis of substituted NH-1,2,3-triazoles, single-phase CS nanoparticles (i.e., CuS) provided the best catalytic result. This significant outcome certainly opens up the scope for realizing the present demand of low-cost multifunctional semiconductor nano-materials, which will have a huge impact on the economy and environment when they show more than two potential applications.

Category: alcohols-buliding-blocks. 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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Application In Synthesis of (4-Methoxyphenyl)methanol. Authors Ghosh, R; Jana, NC; Panda, S; Bagh, B in AMER CHEMICAL SOC published article about in [Ghosh, Rahul; Jana, Narayan Ch; Panda, Surajit; Bagh, Bidraha] HBNI, Natl Inst Sci Educ & Res NISER, Sch Chem Sci, Bhubaneswar 752050, Odisha, India in 2021, Cited 111. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Coordination of 1,4-disubstituted 1,2,3-triazoles L-1 and L-2 with [(p-cymene)RuCl2](2) followed by dehydrochlorination in the presence of a base resulted in the formation of complexes 1 and 2, respectively. Both were tested for the transfer hydrogenation of aldehydes and ketones in air using ecologically benign and cheap ethanol as the hydrogen source in the presence of a catalytic amount of a base. Air-stable complex 1 was proved to be an active catalyst for the transfer hydrogenation of a wide variety of aromatic and aliphatic aldehydes and ketones bearing various functionalities. Catalyst 1 was also effective for the transfer hydrogenation of carbonyls using the simplest primary alcohol, methanol, under aerobic conditions. Under the present catalytic protocol, labile or reducible functionalities such as nitro, cyano, and ester groups were tolerated. Good selectivity was also observed for acyclic alpha,beta-unsaturated carbonyls. However, this catalytic protocol was not selective for 2-cyclohexen-1-one as both alkene and keto moieties were reduced. The transfer hydrogenations are believed to proceed via a ruthenium-hydride intermediate. Finally, transfer hydrogenation of acetophenone using isopropanol as a commonly used hydrogen source was also performed and the sustainable and green credentials of these catalytic protocols utilizing methanol, ethanol, and isopropanol were compared with the help of the CHEM21 green metrics toolkit.

Application In Synthesis of (4-Methoxyphenyl)methanol. Welcome to talk about 105-13-5, If you have any questions, you can contact Ghosh, R; Jana, NC; Panda, S; Bagh, B or send Email.

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HPLC of Formula: C8H10O2. Midya, SP; Subaramanian, M; Babu, R; Yadav, V; Balaraman, E in [Midya, Siba P.; Subaramanian, Murugan; Babu, Reshma; Balaraman, Ekambaram] Indian Inst Sci Educ & Res IISER Tirupati, Dept Chem, Tirupati 517507, Andhra Pradesh, India; [Yadav, Vinita] CSIR Natl Chem Lab CSIR NCL, Organ Chem Div, Pune 411008, Maharashtra, India published Tandem Acceptorless Dehydrogenative Coupling-Decyanation under Nickel Catalysis in 2021, Cited 55. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

The development of new catalytic processes based on abundantly available starting materials by cheap metals is always a fascinating task and marks an important transition in the chemical industry. Herein, a nickel-catalyzed acceptorless dehydrogenative coupling of alcohols with nitriles followed by decyanation of nitriles to access diversely substituted olefins is reported. This unprecedented C=C bond-forming methodology takes place in a tandem manner with the formation of formamide as a sole byproduct. The significant advantages of this strategy are the low-cost nickel catalyst, good functional group compatibility (ether, thioether, halo, cyano, ester, amino, N/O/S heterocycles; 43 examples), synthetic convenience, and high reaction selectivity and efficiency.

Welcome to talk about 105-13-5, If you have any questions, you can contact Midya, SP; Subaramanian, M; Babu, R; Yadav, V; Balaraman, E or send Email.. HPLC of Formula: C8H10O2

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SDS of cas: 105-13-5. Authors Sato, K; Tanaka, S; Wang, JZ; Ishikawa, K; Tsuda, S; Narumi, T; Yoshiya, T; Mase, N in AMER CHEMICAL SOC published article about in [Sato, Kohei; Tanaka, Shoko] Shizuoka Univ, Grad Sch Sci & Technol, Hamamatsu, Shizuoka 4328561, Japan; [Wang, Junzhen; Ishikawa, Kenya] Shizuoka Univ, Dept Appl Chem & Biochem Engn, Fac Engn, Hamamatsu, Shizuoka 4328561, Japan; [Tsuda, Shugo; Yoshiya, Taku] Peptide Inst Inc, Ibaraki, Osaka 5670085, Japan; [Narumi, Tetsuo; Mase, Nobuyuki] Shizuoka Univ, Dept Appl Chem & Biochem Engn, Fac Engn,Grad Sch Sci & Technol, Course Appl Chem & Biochem Engn,Dept Engn,Grad Sc, Hamamatsu, Shizuoka 4328561, Japan; [Narumi, Tetsuo; Mase, Nobuyuki] Shizuoka Univ, Res Inst Green Sci & Technol, Hamamatsu, Shizuoka 4328561, Japan; [Sato, Kohei] Shizuoka Univ, Dept Appl Chem & Biochem Engn, Fac Engn, Course Appl Chem & Biochem Engn,Dept Engn,Grad Sc, Hamamatsu, Shizuoka 4328561, Japan in 2021, Cited 52. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A novel late-stage solubilization of peptides using hydrazides is described. A solubilizing tag was attached through a selective N-alkylation at a hydrazide moiety with the aid of a 2-picoline-borane complex in 50% acetic acid-hexafluoro-2-propanol. The tag, which tolerates ligation and desulfurization conditions, can be detached by a Cu-mediated selective oxidative hydrolysis of the N-alkyl hydrazide. This new method was validated through the synthesis of HIV-1 protease.

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HPLC of Formula: C8H10O2. Authors Das, MK; Yadav, A; Majumder, S; Mondal, A; Bisai, A in PERGAMON-ELSEVIER SCIENCE LTD published article about in [Das, Mrinal K.; Yadav, Abhinay; Majumder, Satyajit; Bisai, Alakesh] Indian Inst Sci Educ & Res Bhopal, Dept Chem, Bhopal 462066, Madhya Pradesh, India; [Mondal, Ayan; Bisai, Alakesh] Indian Inst Sci Educ & Res Kolkata, Dept Chem, Nadia 741246, W Bengal, India in 2021, Cited 41. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

An efficient Pd(0)-catalyzed deacylative allylation (DaA) of enolcarbonates (pro-nucleophile) prepared from 2-arylcyclohexanones sharing acyl functionality at C2-position with readily available allylic alcohols (pro-electrophiles) by employing Pd(0)-catalysis under mild reaction conditions. The methodology can be extended for deacylative benzylations (DaB) of enolcarbonates of 2-arylcyclohexanones. As an application of our methodology, we have shown asymmetric total synthesis of Amaryllidaceae alkaloids, (+)- and (-)-crinane. (C) 2021 Published by Elsevier Ltd.

Welcome to talk about 105-13-5, If you have any questions, you can contact Das, MK; Yadav, A; Majumder, S; Mondal, A; Bisai, A or send Email.. HPLC of Formula: C8H10O2

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COA of Formula: C8H10O2. Authors Sung, K; Lee, MH; Cheong, YJ; Kim, YK; Yu, S; Jang, HY in WILEY-V C H VERLAG GMBH published article about in [Sung, Kihyuk; Lee, Mi-hyun; Cheong, Yeon-Joo; Kim, Yu Kwon; Yu, Sungju; Jang, Hye-Young] Ajou Univ, Dept Energy Syst Res, Suwon 16499, South Korea in 2021, Cited 56. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Multi N-heterocyclic carbene(NHC)-modified iridium catalysts were employed in the beta-alkylation of alcohols; dimerization of primary alcohols (Guerbet reaction), cross-coupling of secondary and primary alcohols, and intramolecular cyclization of alcohols. Mechanistic studies of Guerbet reaction, including kinetic experiments, mass analysis, and density functional theory (DFT) calculation, were employed to explain the fast reaction promoted by bimetallic catalysts, and the dramatic reactivity increase of monometallic catalysts at the late stage of the reaction.

COA of Formula: C8H10O2. 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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Recently I am researching about ONE-POT SYNTHESIS; BORROWING HYDROGEN; 2-SUBSTITUTED BENZIMIDAZOLES; TRANSITION-METAL; N-ALKYLATION; SELECTIVE HYDROGENATION; CHEMOSELECTIVE HYDROGENATION; QUINOXALINE DERIVATIVES; SWITCHABLE SYNTHESIS; AROMATIC DIAMINES, Saw an article supported by the Universite de Rennes 1, the CNRS; Chinese Fellowship Council. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Wu, JJ; Darcel, C. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol. Computed Properties of C8H10O2

A straightforward and selective reduction of nitroarenes with various alcohols was efficiently developed using an iron catalyst via a hydrogen transfer methodology. This protocol led specifically to imines in 30-91% yields, with a good functional group tolerance. Noticeably, starting from o-nitroaniline derivatives, in the presence of alcohols, benzimidazoles can be obtained in 64-72% yields when the reaction was performed with an additional oxidant, DDQ, and quinoxalines were prepared from 1,2-diols in 28-96% yields. This methodology, unprecedented at iron for imines, also provides a sustainable alternative for the preparation of quinoxalines and benzimidazoles.

Computed Properties of C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Wu, JJ; Darcel, C or send Email.

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