Tag: M.W=100-150

Authors Wang, K; Chen, H; Dai, XY; Huang, XP; Feng, ZQ in ROYAL SOC CHEMISTRY published article about CASCADE SYNTHESIS; QUINAZOLINONES; SYSTEM; 4(3H)-QUINAZOLINONES; 2-NITROBENZAMIDES; AMINOBENZAMIDES; CYCLIZATION; CHEMISTRY; EFFICIENT; STRATEGY in [Wang, Ke; Chen, Hao; Dai, Xinyan; Huang, Xupeng; Feng, Zhiqiang] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, Beijing Key Lab Act Subst Discovery & Drugabil Ev, 1 Xiannongtan St, Beijing 100050, Peoples R China in 2021, Cited 41. Name: (4-Methoxyphenyl)methanol. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Palladium-catalyzed 2-substituted quinazolin-4(3H)-one formation from readily available o-nitrobenzamides and alcohols using hydrogen transfer is described. Various quinazolin-4(3H)-ones were obtained in good to high yields. The cascade reaction including alcohol oxidation, nitro reduction, condensation, and dehydrogenation occurs without any added reducing or oxidizing agent.

Name: (4-Methoxyphenyl)methanol. Welcome to talk about 105-13-5, If you have any questions, you can contact Wang, K; Chen, H; Dai, XY; Huang, XP; Feng, ZQ or send Email.

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Safety 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.

Safety 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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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. Safety of (4-Methoxyphenyl)methanol. 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.

Welcome to talk about 105-13-5, If you have any questions, you can contact Sato, K; Tanaka, S; Wang, JZ; Ishikawa, K; Tsuda, S; Narumi, T; Yoshiya, T; Mase, N or send Email.. Safety of (4-Methoxyphenyl)methanol

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Product Details of 105-13-5. Authors Feng, XY; Pi, YH; Song, Y; Xu, ZW; Li, Z; Lin, WB in AMER CHEMICAL SOC published article about in [Feng, Xuanyu; Pi, Yunhong; Song, Yang; Xu, Ziwan; Lin, Wenbin] Univ Chicago, Dept Chem, Chicago, IL 60637 USA; [Pi, Yunhong; Li, Zhong] South China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Peoples R China in 2021, Cited 63. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

We report here the construction of two metal-organic frameworks (MOFs), Zr-6-Cu/Fe-1 and Zr-6–Cu/Fe-2, by integrating earth-abundant cuprous photosensitizers (Cu-PSs) and Fe catalysts for photocatalytic aerobic oxidation. Site isolation and pore confinement stabilize both Cu-PSs and Fe catalysts, while the proximity between active centers facilitates electron and mass transfer. Upon visible light irradiation and using O-2 as the only oxidant, Zr-6-Cu/Fe-1 and Zr-6-Cu/ Fe-2 efficiently oxidize alcohols and benzylic compounds to afford corresponding carbonyl products with broad substrate scopes, high turnover numbers of up to 500 with a 9.4-fold enhancement over homogeneous analogues, and excellent recyclability in four consecutive runs. Control experiments, spectroscopic evidence, and computational studies revealed the photooxidation mechanism: oxidative quenching of [Cu-PS]* by O-2 affords [Cu-II-PS], which efficiently oxidizes Fe-III-OH to generate a hydroxyl radical for substrate oxidation. This work highlights the potential of MOFs in promoting earth-abundant metal-based photocatalysis.

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.. Product Details of 105-13-5

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An article Half-sandwich Ru(II) arene complexes bearing benzimidazole ligands for the N-alkylation reaction of aniline with alcohols in a solvent-free medium WOS:000658013400001 published article about RUTHENIUM(II) COMPLEXES; CATALYTIC EFFICIENCY; HYDROGEN-TRANSFER; SECONDARY-AMINES; DISCOVERY; OXIDATION; AMINATION; IMINES in [Cicek, Metin; Ispir, Esin] Kahramanmaras Sutcu Imam Univ, Dept Chem, Fac Sci & Arts, TR-46050 Kahramanmaras 9, Turkey; [Cicek, Metin; Gurbuz, Nevin; Ozdemir, Ismail] Inonu Univ, Catalysis Res & Applicat Ctr, TR-44280 Malatya, Turkey; [Gurbuz, Nevin; Ozdemir, Ismail] Inonu Univ, Dept Chem, Fac Sci & Art, TR-44280 Malatya, Turkey; [Ozdemir, Namik] Ondokuz Mayis Univ, Dept Math & Sci Educ, Fac Educ, TR-9055139 Samsun, Turkey in 2021, Cited 71. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. COA of Formula: C8H10O2

In this article, the direct N-alkylation reactions of amines with alcohol derivatives using the borrowing hydrogen methodology have been investigated. For this purpose, a new series of half-sandwich ruthenium(II) complexes bearing N-coordinated benzimidazole complexes have been synthesized and fully characterized by FT-IR, H-1 NMR and C-13 NMR spectroscopies. Additionally, the structures of the complexes 2a-2e have been characterized by X-ray crystallography. ALL new complexes were investigated for their catalytic activities in the alkylation reaction of amines with alcohol derivatives. It was found that alkylation reactions in a solvent-free medium are efficient and selective.

Welcome to talk about 105-13-5, If you have any questions, you can contact Cicek, M; Gurbuz, N; Ozdemir, N; Ozdemir, I; Ispir, E or send Email.. COA of Formula: C8H10O2

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An article Ultrasmall amphiphilic zeolitic nanoreactors for the aerobic oxidation of alcohols in water WOS:000649428200001 published article about METAL-ORGANIC FRAMEWORK; SELECTIVE OXIDATION; SOLID NANOPARTICLES; CATALYZED REACTIONS; PHASE INVERSION; EMULSIONS; PARTICLES; INTERFACE; CLUSTERS; SIZE in [Jing, Wendan; Li, Hui; Liu, Bolun; Wang, Runwei; Qiu, Shilun; Zhang, Zongtao] Jilin Univ, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China; [Xiao, Peiwen; Luo, Jianhui] PetroChina, Res Inst Petr Explorat & Dev, Beijing 100083, Peoples R China; [Xiao, Peiwen; Luo, Jianhui] CNPC, Key Lab Nano Chem KLNC, Beijing 100083, Peoples R China in 2021, Cited 43. HPLC of Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Organic reactors in a green solvent (water) is the goal of sustainable development. Green nanoreactors with excellent amphiphilicity and catalytic activity are strongly desired. Herein, a novel amphiphilic nanoreactor Pd@amZSM-5 with ultrasmall size has been successfully synthesized via a simple one-step oil bath method, subjected to the modification-etching-modification strategy and in situ reduction of Pd2+. Ultrasmall Pd@amZSM-5 nanoreactors (60 nm) with hierarchical structures showed outstanding amphiphilicity for forming Pickering emulsions with fine uniform droplets (50 mu m). Fine droplets formed short diffusion distances, which can significantly improve the catalytic activity in biphasic reactions. Moroever, the ultrasmall Pd@amZSM-5 nanoreactors demonstrated excellent catalytic activity for the selective oxidation of alcohols in water using air as the oxidant. Alkali was not present in the reaction system. The hydrophilic aminopropyl groups on the surface of the Pd@amZSM-5 nanoreactors not only changed the affinity of the zeolite surface and provided targeting points for Pd nanoparticles but also provided an alkaline environment for the selective oxidation of alcohols. The ultrasmall Pd@amZSM-5 nanoreactors presented excellent universality for aromatic alcohols (with >90% conversion and >90% selectivity) and allylic alcohols (with 100% conversion and 100% selectivity).

HPLC of Formula: C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Jing, WD; Li, H; Xiao, PW; Liu, BL; Luo, JH; Wang, RW; Qiu, SL; Zhang, ZT or send Email.

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An article Half-sandwich Ru(II) arene complexes bearing benzimidazole ligands for the N-alkylation reaction of aniline with alcohols in a solvent-free medium WOS:000658013400001 published article about RUTHENIUM(II) COMPLEXES; CATALYTIC EFFICIENCY; HYDROGEN-TRANSFER; SECONDARY-AMINES; DISCOVERY; OXIDATION; AMINATION; IMINES in [Cicek, Metin; Ispir, Esin] Kahramanmaras Sutcu Imam Univ, Dept Chem, Fac Sci & Arts, TR-46050 Kahramanmaras 9, Turkey; [Cicek, Metin; Gurbuz, Nevin; Ozdemir, Ismail] Inonu Univ, Catalysis Res & Applicat Ctr, TR-44280 Malatya, Turkey; [Gurbuz, Nevin; Ozdemir, Ismail] Inonu Univ, Dept Chem, Fac Sci & Art, TR-44280 Malatya, Turkey; [Ozdemir, Namik] Ondokuz Mayis Univ, Dept Math & Sci Educ, Fac Educ, TR-9055139 Samsun, Turkey in 2021, Cited 71. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. HPLC of Formula: C8H10O2

In this article, the direct N-alkylation reactions of amines with alcohol derivatives using the borrowing hydrogen methodology have been investigated. For this purpose, a new series of half-sandwich ruthenium(II) complexes bearing N-coordinated benzimidazole complexes have been synthesized and fully characterized by FT-IR, H-1 NMR and C-13 NMR spectroscopies. Additionally, the structures of the complexes 2a-2e have been characterized by X-ray crystallography. ALL new complexes were investigated for their catalytic activities in the alkylation reaction of amines with alcohol derivatives. It was found that alkylation reactions in a solvent-free medium are efficient and selective.

Welcome to talk about 105-13-5, If you have any questions, you can contact Cicek, M; Gurbuz, N; Ozdemir, N; Ozdemir, I; Ispir, E or send Email.. HPLC of Formula: C8H10O2

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Application In Synthesis of (4-Methoxyphenyl)methanol. Authors Yoshida, Y; Kukita, M; Omori, K; Mino, T; Sakamoto, M in ROYAL SOC CHEMISTRY published article about in [Yoshida, Yasushi; Kukita, Mayu; Omori, Kazuki; Mino, Takashi; Sakamoto, Masami] Chiha Univ, Grad Sch Engn, Mol Chiral Res Ctr, Inage Ku, 1-33 Yayoi Cho, Chiba, Chiba 2638522, Japan in 2021, Cited 96. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Umpolung reactions of imines, especially the asymmetric reactions, have been extensively studied as they provide access to important chiral amines in an efficient manner. The reactions studied range from simple Michael reactions to several kinds of other reactions such as the aza-benzoin reaction, aza-Stetter reaction, addition with MBH carbonate, and Ir-catalysed allylation. Herein, we report the first umpolung alkylation reaction of alpha-iminoesters with alkyl halides mediated by iminophosphorane as an organic superbase. The desired products were obtained in up to 82% yield with almost perfect regioselectivities. The key to the regioselectivity of this reaction was the use of 4-trifluoromethyl benzyl imines as a substrate. The products were successfully derivatised into the more functionalised molecules in good yields.

Welcome to talk about 105-13-5, If you have any questions, you can contact Yoshida, Y; Kukita, M; Omori, K; Mino, T; Sakamoto, M or send Email.. Application In Synthesis of (4-Methoxyphenyl)methanol

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Name: (4-Methoxyphenyl)methanol. Kuriyama, Y; Sasano, Y; Hoshino, Y; Uesugi, S; Yamaichi, A; Iwabuchi, Y in [Kuriyama, Yuse; Sasano, Yusuke; Hoshino, Yoshihiko; Uesugi, Shun-ichiro; Yamaichi, Aoto; Iwabuchi, Yoshiharu] Tohoku Univ, Dept Organ Chem, Grad Sch Pharmaceut Sci, Aoba Ku, 6-3 Aoba, Sendai, Miyagi 9808578, Japan published Highly Regioselective 5-endo-tet Cyclization of 3,4-Epoxy Amines into 3-Hydroxypyrrolidines Catalyzed by La(OTf)(3) in 2021, Cited 38. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Highly regioselective intramolecular aminolysis of 3,4-epoxy amines has been achieved. Key features of this reaction are (1) chemoselective activation of epoxides in the presence of unprotected aliphatic amines in the same molecules by a La(OTf)(3) catalyst and (2) excellent regioselectivity for anti-Baldwin 5-endo-tet cyclization. This reaction affords 3-hydroxy-2-alkylpyrrolidines stereospecifically in high yields. DFT calculations revealed that the regioselectivity might be attributed to distortion energies of epoxy amine substrates. The use of this reaction was demonstrated by the first enantioselective synthesis of an antispasmodic agent prifinium bromide.

Name: (4-Methoxyphenyl)methanol. Welcome to talk about 105-13-5, If you have any questions, you can contact Kuriyama, Y; Sasano, Y; Hoshino, Y; Uesugi, S; Yamaichi, A; Iwabuchi, Y or send Email.

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COA of Formula: C8H10O2. Authors Song, JL; Hua, ML; Huang, X; Visa, A; Wu, TB; Fan, HL; Hou, MQ; Zhang, ZF; Han, BX in ROYAL SOC CHEMISTRY published article about in [Song, Jinliang; Hua, Manli; Huang, Xin; Wu, Tianbin; Fan, Honglei; Hou, Minqiang; Zhang, Zhaofu; Han, Buxing] Chinese Acad Sci, CAS Key Lab Colloid & Interface & Thermodynam, CAS Res Educ Ctr Excellence Mol Sci, Beijing Natl Lab Mol Sci,Inst Chem, Beijing 100190, Peoples R China; [Hua, Manli; Huang, Xin; Han, Buxing] Univ Chinese Acad Sci, Sch Chem & Chem Engn, Beijing 100049, Peoples R China; [Visa, Aurelia] Romanian Acad, Inst Chem Timisoara, 24 M Viteazul Ave, Timisoara 300223, Romania in 2021, Cited 44. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

The Meerwein-Ponndorf-Verley (MPV) reaction is an attractive approach to selectively reduce carbonyl groups, and the design of advanced catalysts is the key for these kinds of interesting reactions. Herein, we fabricated a novel zirconium organoborate using 1,4-benzenediboronic acid (BDB) as the precursor for MPV reduction. The prepared Zr-BDB had excellent catalytic performance for the MPV reduction of various biomass-derived carbonyl compounds (i.e., levulinate esters, aldehydes and ketones). More importantly, the number of borate groups on the ligands significantly affected the catalytic activity of the Zr-organic ligand hybrids, owing to the activation role of borate groups on hydroxyl groups in the hydrogen source. Detailed investigations revealed that the excellent performance of Zr-BDB was contributed by the synergetic effect of Zr4+ and borate. Notably, this is the first work to enhance the activity of Zr-based catalysts in MPV reactions using borate groups.

Welcome to talk about 105-13-5, If you have any questions, you can contact Song, JL; Hua, ML; Huang, X; Visa, A; Wu, TB; Fan, HL; Hou, MQ; Zhang, ZF; Han, BX or send Email.. COA of Formula: C8H10O2

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