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Journal articles on the topic '4-Methoxybenzyl Alcohol'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 September 2023

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1

Firdaus, Maulidan, Jumina Jumina, and Chairil Anwar. "GREEN CHEMISTRY APPLICATION FOR THE SYNTHESIS OF (1)-N-4’-METHOXYBENZYL-1,10-PHENANTHROLINIUM BROMIDE." Indonesian Journal of Chemistry 8, no. 3 (2010): 423–25. http://dx.doi.org/10.22146/ijc.21611.

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A simple, energy-efficient, and relatively quick synthetic procedure for the synthesis of (1)-N-4'-methoxybenzyl-1,10-phenanthrolinium bromide, based on green chemistry principles has been carried out. The synthesis was started by solvent-free reduction of p-anisaldehyde with NaBH4 to give 4-methoxybenzyl alcohol in 98% yield to be followed by solvent-free treatment of the resulted alcohol with PBr3 to yield 4-methoxybenzyl bromide (86%). Furthermore, the obtained bromide was reacted with 1,10-phenanthroline in acetone at reflux for 12 h to give the phenanthrolinium salt target in 68% yield. K

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2

Hadanu, Ruslin, Sabirin Mastjeh, Jumina Jumina, Mustofa Mustofa, Mahardika Agus Widjayanti, and Eti Nurwening Sholikhah. "SYNTHESIS AND ANTIPLASMODIAL ACTIVITY TESTING OF (1)-N-(4-METHOXYBENZYL)-1,10-PHENANTHROLINIUM BROMIDE." Indonesian Journal of Chemistry 7, no. 2 (2010): 197–201. http://dx.doi.org/10.22146/ijc.21698.

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Synthesis of (1)-N-(4-methoxybenzyl)-1,10-phenanthroline bromide from 1,10-phenanthroline monohydrate and 4-methoxybenzaldehyde as starting material and evaluation of its antiplasmodial activities have been carried out. The 4-methoxybenzyl alcohol was prepared from 4-methoxy-benzaldehyde using sodium borohydride (NaBH4) reagent and ethanol absolute solution. The mixture was refluxed for 3 h. To yield colorless dilution compound with 90.41 % in efficiency. Furthermore, bromination of 4-methoxybenzyl alcohol with phosphorus bromide (PBr3) was conducted by refluxing for 3 h. The product of this r

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3

Batalini, Claudemir, and Wagner Ferraresi De Giovani. "FELT CARBON ELECTRODES MODIFIED WITH RUTHENIUM DIMERIC FILM: APPLICATION IN ALCOHOL ELECTROCHEMICAL OXIDATIONS." Eclética Química Journal 39, no. 1 (2017): 1. http://dx.doi.org/10.26850/1678-4618eqj.v39.1.2014.p1-11.

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Modified films were prepared by deposition of poli-[(H2O)(L)2Ru-O-Ru(L)2(OH2)]4+ (L=4-methyl- 4´-pyrrol-1-yl-buthyl-2,2´-bipyridine) (poly-dim.), on felt carbon electrodes, by direct anodic electropolymerization of the monomer. The electrocatalyst activity of these modified carbon felt carbon electrodes was tested in alcohols oxidations, at constant potential +1.15 V (vs SCE), in 1.0 and 6.8 pH. The started alcohols and the products were: benzyl alcohol (benzaldehyde), cycloexanol (cyclohexanone), 1-phenylethanol (acetophenone) and p-methoxybenzyl alcohol (p-methoxybenzaldehyde). The reactions

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4

Fu, Wei, Lumin Yue, Xiaogang Duan, Jun Li, and Guanzhong Lu. "Acceptor-free dehydrogenation of 4-hydroxy-3-methoxybenzyl alcohol to vanillin over a palladium complex." Green Chemistry 18, no. 22 (2016): 6136–42. http://dx.doi.org/10.1039/c6gc01855f.

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5

Arce, Valeria B., Sonia G. Bertolotti, Fernando J. V. E. Oliveira, et al. "Triplet state of 4-methoxybenzyl alcohol chemisorbed on silica nanoparticles." Photochemical & Photobiological Sciences 11, no. 6 (2012): 1032. http://dx.doi.org/10.1039/c2pp05370e.

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6

Darzac, Magali, Stéphanie Montésinos, André Collet, and Jean-Pierre Dutasta. "Synthesis of Complementary Hydrogen Bonding Cyclotriveratrylenes." Journal of Chemical Research 2002, no. 8 (2002): 359–60. http://dx.doi.org/10.3184/030823402103172482.

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Two new cyclotriveratrylenes CTV-1 and CTV-2 bearing complementary H-bond donor-acceptor substituents were prepared from 4-hydroxy-3-methoxybenzyl alcohol following a multistep strategy to introduce melamine or cyanuric acid substituents.

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7

Davidson, Ross J., Lucy E. Wilson, Andrew R. Duckworth, Dmitry S. Yufit, Andrew Beeby, and Paul J. Low. "Alkyne substituted mononuclear photocatalysts based on [RuCl(bpy)(tpy)]+." Dalton Transactions 44, no. 25 (2015): 11368–79. http://dx.doi.org/10.1039/c5dt01278c.

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The introduction of ‘wire-like’ arylene ethynylene substituent to the prototypical water oxidation catalyst precursor [RuCl(2,2′-bipyridine)(2,2′:6′,2′′-terpyridine)]PF<sub>6</sub>does not significantly alter the photostability of the compounds, nor the ability of the complexes to oxidise 4-methoxybenzyl alcohol to 4-methoxybenzaldehyde.

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8

Tóth, M., A. Nagy, I. Szarukán, et al. "One Decade’s Research Efforts in Hungary to Develop a Bisexual Lure for the Cotton Bollworm Helicoverpa armigera Hübner." Acta Phytopathologica et Entomologica Hungarica 55, no. 1 (2020): 79–88. http://dx.doi.org/10.1556/038.55.2020.005.

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The addition of synthetic (E)-anethol to the known attractant phenylacetaldehyde synergized attraction of the cotton bollworm Helicoverpa armigera, the blend invariably catching 4 to 6 times more than phenylacetaldehyde on its own. Highest catches were recorded by the 1:1-3:1 blends. The addition of salicyl aldehyde, ±linalool, (R)-(+)-limonene, 2-methoxybenzyl alcohol and 4-methoxybenzyl alcohol (compounds described earlier in the literature as co-attractants for H. armigera), increased catches when added to phenylacetaldehyde. However, the addition of these compounds did not increase catches

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9

Bourbonnais, R., and M. G. Paice. "Veratryl alcohol oxidases from the lignin-degrading basidiomycete Pleurotus sajor-caju." Biochemical Journal 255, no. 2 (1988): 445–50. http://dx.doi.org/10.1042/bj2550445.

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The basidiomycete Pleurotus sajor-caju mineralizes ring-14C-labelled lignin (dehydrogenative polymer) when grown in mycological broth. Under these conditions, two veratryl alcohol oxidase (VAO) enzymes were found in the culture medium. They oxidized a number of aromatic alcohols to aldehydes and reduced O2 to H2O2. The enzymes were purified by ion-exchange and gel-permeation chromatography. The final step of purification on Mono Q resolved the activity into two peaks (VAO I and VAO II). Both enzymes had the same Mr, approx. 71,000, but their isoelectric points differed slightly, 3.8 for VAO I

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10

Cibulka, Radek, Rudolf Vasold, and Burkhard König. "Catalytic Photooxidation of 4-Methoxybenzyl Alcohol with a Flavin-Zinc(II)-Cyclen Complex." Chemistry - A European Journal 10, no. 24 (2004): 6223–31. http://dx.doi.org/10.1002/chem.200400232.

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11

García-López, Elisa I., Zahra Abbasi, Francesco Parrino, Valeria La Parola, Leonarda F. Liotta, and Giuseppe Marcì. "Au/CeO2 Photocatalyst for the Selective Oxidation of Aromatic Alcohols in Water under UV, Visible and Solar Irradiation." Catalysts 11, no. 12 (2021): 1467. http://dx.doi.org/10.3390/catal11121467.

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Au nanoparticles supported on CeO2 have been prepared and investigated as photocatalysts for the photocatalytic selective oxidation of benzyl alcohol and 4-methoxybenzyl alcohol to the correspondent benzaldehydes, in aqueous suspensions and room conditions under UV, visible and natural solar light irradiation. Au nanoparticles have been supported by impregnation (1 and 3 wt.%) on two types of CeO2 (i.e., a commercial one and a home prepared oxide obtained in the presence of NaOH as precipitation agent). The Au impregnated samples showed strong visible radiation absorption at 565–570 nm associa

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12

Turkowicz, Monika, Izabella Jastrzebska, Marta Hryniewicka, Urszula Kotowska, Diana Gudalewska, and Joanna Karpińska. "Investigation of lipoic acid – 4-methoxybenzyl alcohol reaction and evaluation of its analytical usefulness." Food Chemistry 309 (March 2020): 125750. http://dx.doi.org/10.1016/j.foodchem.2019.125750.

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13

Yurdakal, Sedat, Vittorio Loddo, Giovanni Palmisano, Vincenzo Augugliaro, Hüseyin Berber, and Leonardo Palmisano. "Kinetics of 4-Methoxybenzyl Alcohol Oxidation in Aqueous Solution in a Fixed Bed Photocatalytic Reactor." Industrial & Engineering Chemistry Research 49, no. 15 (2010): 6699–708. http://dx.doi.org/10.1021/ie9008056.

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14

Özcan, Levent, Sedat Yurdakal, Vincenzo Augugliaro, et al. "Photoelectrocatalytic selective oxidation of 4-methoxybenzyl alcohol in water by TiO2 supported on titanium anodes." Applied Catalysis B: Environmental 132-133 (March 2013): 535–42. http://dx.doi.org/10.1016/j.apcatb.2012.12.030.

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15

Černý, Ivan, Tereza Slavíková та Vladimír Pouzar. "Synthesis of (15E)-17β-hydroxy-5α-androstane-3,15-dione 15-[O-(Carboxymethyl)]oxime, New Hapten for Dihydrotestosterone (17β-hydroxy-5α-androstan-3-one)". Collection of Czechoslovak Chemical Communications 62, № 10 (1997): 1642–49. http://dx.doi.org/10.1135/cccc19971642.

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Addition of 4-methoxybenzyl alcohol to 3β-hydroxy-5α-androst-15-en-17-one gave the mixture of isomeric 15-(4-methoxyphenyl)methoxy derivatives from which, after acetylation and chromatography, the major 15β isomer was separated. Borohydride reduction gave 17β-hydroxy derivative which was protected as methoxymethyl ether. Oxidative cleavage of protecting group at position 15 and the subsequent Jones oxidation afforded corresponding 15-ketone. Its oximation with O-(carboxymethyl)hydroxylamine, deacetylation and methylation with diazomethane gave protected O-(carboxymethyl)oxime derivative with f

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16

Bettoni, Marta, Pietro Candori, Fabio Marmottini, et al. "Photocatalytic Activity inCH3CN Related to the Surface Properties ofTiO2Powders Prepared by Sol-Gel Method." International Journal of Photoenergy 2009 (2009): 1–6. http://dx.doi.org/10.1155/2009/905987.

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SomeTiO2powders, prepared from titanium(IV)tetraisopropoxide by the sol-gel method and thermally treated between 100 and1000∘C, have been characterized by X-ray powder diffraction and by nitrogen adsorption and desorption at 77 K to calculate the BET-specific surface area, from which the micropore volume and the external surface area can be derived. The photocatalytic activity (ka) of the above powders has been evaluated considering theTiO2-sensitized photo-oxidation of 4-methoxybenzyl alcohol inCH3CN as the test reaction. The decrease ofkahave been related to the decrease of the BET surface a

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17

Bellardita, Marianna, Sedat Yurdakal, Bilge Sina Tek, et al. "Tuning the selectivity to aldehyde via pH regulation in the photocatalytic oxidation of 4-methoxybenzyl alcohol and vanillyl alcohol by TiO2 catalysts." Journal of Environmental Chemical Engineering 9, no. 4 (2021): 105308. http://dx.doi.org/10.1016/j.jece.2021.105308.

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18

Del Giacco, Tiziana, Annalisa Faltoni, and Fausto Elisei. "Anomalous reactivity of radical cations produced by photosensitized oxidation of 4-methoxybenzyl alcohol derivatives: role of the sensitizer." Phys. Chem. Chem. Phys. 10, no. 1 (2008): 200–210. http://dx.doi.org/10.1039/b711541e.

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19

Bettoni, Marta, Sara Meniconi, Cesare Rol, and Giovanni V. Sebastiani. "Selective photocatalytic oxidation at TiO2/Ti anodes of 4-methoxybenzyl alcohol to the corresponding benzaldehyde in “green” conditions." Journal of Photochemistry and Photobiology A: Chemistry 222, no. 1 (2011): 180–84. http://dx.doi.org/10.1016/j.jphotochem.2011.05.019.

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20

Palmisano, Giovanni, Sedat Yurdakal, Vincenzo Augugliaro, Vittorio Loddo, and Leonardo Palmisano. "Photocatalytic Selective Oxidation of 4-Methoxybenzyl Alcohol to Aldehyde in Aqueous Suspension of Home-Prepared Titanium Dioxide Catalyst." Advanced Synthesis & Catalysis 349, no. 6 (2007): 964–70. http://dx.doi.org/10.1002/adsc.200600435.

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21

Czulak, Joanna, Anna Jakubiak-Marcinkowska, and Andrzej Trochimczuk. "Polymer Catalysts Imprinted with Metal Ions as Biomimics of Metalloenzymes." Advances in Materials Science and Engineering 2013 (2013): 1–9. http://dx.doi.org/10.1155/2013/464265.

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This work presents the preparation and properties of molecularly imprinted polymers (MIPs) with catalytic centers that mimic the active sites of metalloenzymes. The MIP synthesis was based on suspension polymerization of functional monomers (4-vinylpyridine and acrylonitrile) with trimethylolpropane trimethacrylate as a crosslinker in the presence of transition metal ions and 4-methoxybenzyl alcohol as a template. Four metal ions have been chosen for imprinting from among the microelements that are the most essential in the native enzymes: Cu2+, Co2+, Mn2+, and Zn2+. To prepare catalysts, the

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22

Castellan, Alain, Stéphane Grelier, Larbi Kessab, Aziz Nourmamode та Yacine Hannachi. "Photophysics and photochemistry of a lignin model molecule containing α-carbonyl guaiacyl and 4-hydroxy-3-methoxybenzyl alcohol moieties". J. Chem. Soc., Perkin Trans. 2, № 6 (1996): 1131–38. http://dx.doi.org/10.1039/p29960001131.

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23

Zieniuk, Bartłomiej, Katarzyna Groborz, Małgorzata Wołoszynowska, Katarzyna Ratusz, Ewa Białecka-Florjańczyk, and Agata Fabiszewska. "Enzymatic Synthesis of Lipophilic Esters of Phenolic Compounds, Evaluation of Their Antioxidant Activity and Effect on the Oxidative Stability of Selected Oils." Biomolecules 11, no. 2 (2021): 314. http://dx.doi.org/10.3390/biom11020314.

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The aim of the study was to compare the effect of the substituent and its position in the aromatic ring on the antioxidant activity of hexanoic acid esters obtained in reactions catalyzed by immobilized lipase B from Candida antarctica. 4-Hydroxybenzyl hexanoate, 2-hydroxybenzyl hexanoate, 4-methoxybenzyl hexanoate, and vanillyl hexanoate were obtained with conversion yields of 50 to 80%. The antioxidant activity of synthesized esters, their alcohol precursors and BHT (Butylated HydroxyToluene) was compared with DPPH (2,2-diphenyl-1-picrylhydrazyl), CUPRAC (cupric ion reducing antioxidant capa

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24

Hautzel, Ralf, and Heidrun Anke. "Screening of Basidiomycetes and Ascomycetes for Plant Growth Regulating Substances. Introduction of the Gibberellic Acid Induced de-novo Synthesis of Hydrolytic Enzymes in Embryoless Seeds of Triticum aestivum as Test System." Zeitschrift für Naturforschung C 45, no. 11-12 (1990): 1093–98. http://dx.doi.org/10.1515/znc-1990-11-1204.

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Abstract A new test system for the detection of plant growth regulating activities was successfully employed. In a screening for inhibitors of the gibberellic acid controlled synthesis of hydrolytic enzymes in embryoless wheat seeds (Triticum aestivum) 160 cultures of ascomycetes and basidiomycetes were tested. In the extracts of two cultures inhibitory activities were detected. From fermentations of a Hypholoma-species (basidiomycetes) 3,5-dichloro-4-methoxybenzyl alcohol was isolated as the active principle. Galiellalactone and two other new phytotoxins were isolated from cultures of the as

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25

Ho, Hsin-Jung, Natsumi Aoki, Yi-Jou Wu, et al. "A Pacific Oyster-Derived Antioxidant, DHMBA, Protects Renal Tubular HK-2 Cells against Oxidative Stress via Reduction of Mitochondrial ROS Production and Fragmentation." International Journal of Molecular Sciences 24, no. 12 (2023): 10061. http://dx.doi.org/10.3390/ijms241210061.

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The kidney contains numerous mitochondria in proximal tubular cells that provide energy for tubular secretion and reabsorption. Mitochondrial injury and consequent excessive reactive oxygen species (ROS) production can cause tubular damage and play a major role in the pathogenesis of kidney diseases, including diabetic nephropathy. Accordingly, bioactive compounds that protect the renal tubular mitochondria from ROS are desirable. Here, we aimed to report 3,5-dihydroxy-4-methoxybenzyl alcohol (DHMBA), isolated from the Pacific oyster (Crassostrea gigas) as a potentially useful compound. In hum

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26

Amić, Ana, Zoran Marković, Jasmina M. Dimitrić Marković, Dejan Milenković, and Bono Lučić. "The role of guaiacyl moiety in free radical scavenging by 3,5-dihydroxy-4-methoxybenzyl alcohol: thermodynamics of 3H+/3e− mechanisms." Molecular Physics 117, no. 2 (2018): 207–17. http://dx.doi.org/10.1080/00268976.2018.1506174.

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27

Djaballah, Ahmed Malek, Marianna Bellardita, Leonardo Palmisano, et al. "Facile preparation of CuBi2O4/TiO2 hetero-systems employed for simulated solar-light selective oxidation of 4-methoxybenzyl alcohol model compound." Molecular Catalysis 546 (July 2023): 113251. http://dx.doi.org/10.1016/j.mcat.2023.113251.

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28

Xiao, Zhu-Ping, Rui-Qin Fang, Lei Shi, Hui Ding, Chen Xu, and Hai-Liang Zhu. "Synthesis, crystal structure, and growth inhibition of human hepatoma cell (HepG2) of polyphenolic compounds based on gallates." Canadian Journal of Chemistry 85, no. 11 (2007): 951–57. http://dx.doi.org/10.1139/v07-107.

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Seven compounds (1–7) based on gallate were synthesized and characterized by elemental analysis, 1H NMR, and MS spectra. 2-(3,5-Dibenzyloxy-4-methoxy)phenyl-2-propanol (6) was a new compound. Methyl 3,5-dihydroxy-4-methoxybenzoate (3), methyl 3,5-dibenzyloxy-4-methoxybenzoate (4), 3,5-dibenzyloxy-4-methoxybenzyl alcohol (5), and compound 6 were structurally determined by single-crystal X-ray diffraction for the first time. Crystallographic data for 3: space group P212121; a = 4.0750(8) Å, b = 7.5880(15) Å, c = 29.802(6) Å; V = 921.5(3) Å3; Z = 4. 4: space group P-1; a = 10.068(2) Å, b = 10.499

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29

Wood, William F., Allyson Walsh, John Seyjagat, and Paul J. Weldon. "Volatile Compounds in Shoulder Gland Secretions of Male Flying Foxes, Genus Pteropus (Pteropodidae, Chiroptera)." Zeitschrift für Naturforschung C 60, no. 9-10 (2005): 779–84. http://dx.doi.org/10.1515/znc-2005-9-1019.

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Abstract The shoulder gland secretions of captive males of the Indian flying fox (Pteropus giganteus), the little golden-mantled flying fox (P. pumilus), the island flying fox (P. hypomelanus), and the large flying fox (P. vampyrus) were examined by gas chromatography-mass spectrometry. Sixty-five compounds, including hydrocarbons, carboxylic acids, alcohols, aldehydes, ketones, esters, and amides, were identified among the four species. Many of these compounds, such as squalene, cholesterol, and C5-C16 straight- and branched-chain carboxylic acids, are typical of tetrapod epidermal products.

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30

Yamaguchi, Masayoshi, Kenji Yoshiike, Hideaki Watanabe, and Mitsugu Watanabe. "The Marine Factor 3,5-Dihydroxy-4-methoxybenzyl Alcohol Represses Adipogenesis in Mouse 3T3-L1 Adipocytes In Vitro: Regulating Diverse Signaling Pathways." Nutraceuticals 3, no. 3 (2023): 366–79. http://dx.doi.org/10.3390/nutraceuticals3030028.

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The augmentation of adipocytes in the adipose tissues brings disordered pathophysiological conditions, including type 2 diabetes, hyperlipidemia, hypertension, cardiovascular disease, and cancer. The phenolic antioxidant 3,5-dihydroxy-4-methoxybenzyl alcohol (DHMBA) prevents oxidative stress as radical scavenging in cells. However, the role of the disorder as a pharmacologic factor has been poorly understood. This study elucidates the regulatory effects of DHMBA on adipogenesis in mouse 3T3-L1 adipocytes in vitro. The 3T3-L1 preadipocytes were cultured in DMEM containing 10% calf fetal serum i

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31

Boyko, Olexandra, and Viktor Brygadyrenko. "Survival of Nematode Larvae Strongyloides papillosus and Haemonchus contortus under the Influence of Various Groups of Organic Compounds." Diversity 15, no. 2 (2023): 254. http://dx.doi.org/10.3390/d15020254.

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Many chemically synthesized xenobiotics can significantly inhibit the vitality of parasitic nematodes. However, there is yet too little research on the toxicity of such contaminating compounds toward nematodes. Compounds that are present in plants are able to inhibit the vitality of parasitic organisms as well. According to the results of our laboratory studies of toxicity, the following xenobiotics caused no decrease in the vitality of the larvae of Strongyloides papillosus and Haemonchus contortus: methanol, propan-2-ol, propylene glycol-1,2, octadecanol-1, 4-methyl-2-pen-tanol, 2-ethoxyetha

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32

Fukai, Moto, Takuya Nakayabu, Shintaro Ohtani, et al. "The Phenolic Antioxidant 3,5-dihydroxy-4-methoxybenzyl Alcohol (DHMBA) Prevents Enterocyte Cell Death under Oxygen-Dissolving Cold Conditions through Polyphyletic Antioxidant Actions." Journal of Clinical Medicine 10, no. 9 (2021): 1972. http://dx.doi.org/10.3390/jcm10091972.

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Cold preservation in University of Wisconsin (UW) solution is not enough to maintain the viability of the small intestine, due to the oxidative stress. The novel phenolic antioxidant 3,5-dihydroxy-4-methoxybenzyl alcohol (DHMBA) has dual properties to reduce oxidative stress, radical scavenging, and antioxidant protein induction, in other cells. This study was designed to determine whether DHMBA reduces cold preservation injury of enterocytes, and to identify the effector site. Enterocytes were subjected to 48-h cold preservation under atmosphere in UW solution (±DHMBA), and then returned to n

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33

Augugliaro, Vincenzo, Vittorio Loddo, María José López-Muñoz, et al. "Home-prepared anatase, rutile, and brookite TiO2 for selective photocatalytic oxidation of 4-methoxybenzyl alcohol in water: reactivity and ATR-FTIR study." Photochemical & Photobiological Sciences 8, no. 5 (2009): 663. http://dx.doi.org/10.1039/b818353h.

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34

Veličković, Dušan, Aleksandra Dimitrijević, Filip Bihelović, Dejan Bezbradica, Zorica Knežević-Jugović та Nenad Milosavić. "Novel glycoside of vanillyl alcohol, 4-hydroxy-3-methoxybenzyl-α-d-glucopyranoside: study of enzymatic synthesis, in vitro digestion and antioxidant activity". Bioprocess and Biosystems Engineering 35, № 7 (2012): 1107–15. http://dx.doi.org/10.1007/s00449-012-0695-3.

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35

Dai, Rong, Ting Wang, Xiaoqin Si, et al. "Vasodilatory effects and underlying mechanisms of the ethyl acetate extracts from Gastrodia elata." Canadian Journal of Physiology and Pharmacology 95, no. 5 (2017): 564–71. http://dx.doi.org/10.1139/cjpp-2016-0407.

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The objective of this study was to assess the ethyl acetate extracts of Gastrodia elata Blume (GEB) on vascular tone and the mechanisms involved. GEB was extracted with 95% EtOH followed by a further extraction with ethyl acetate. The effects of GEB and its ingredients on the isometric tensions of the aortic rings from rats were measured. The ethyl acetate extract of GEB induced a vasodilatory effect on rat aorta, which was partially dependent on endothelium. Four chemical compounds isolated from GEB were identified as 3,4-dihydroxybenzaldehyde (DB), 4-hydroxybenzaldehyde (HB), 4-methoxybenzyl

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36

Baciocchi, Enrico, Massimo Bietti, and Steen Steenken. "Base-Catalyzed C−H Deprotonation of 4-Methoxybenzyl Alcohol Radical Cations in Water: Evidence for a Carbon-to-Oxygen 1,2-H-Shift Mechanism." Journal of the American Chemical Society 119, no. 17 (1997): 4078–79. http://dx.doi.org/10.1021/ja970259q.

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37

Crich, David, Linfeng Li, and Michio Shirai. "The 4-(tert-Butyldiphenylsiloxy)-3-fluorobenzyl Group: A New Alcohol Protecting Group, Fully Orthogonal with thep-Methoxybenzyl Group and Removable under Desilylation Conditions." Journal of Organic Chemistry 74, no. 6 (2009): 2486–93. http://dx.doi.org/10.1021/jo900026e.

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38

Zhang, Kui-Yong, Nan-ning Lu, Seung Joon Yoo, Li-Ming Hu, R. Daniel Little, and Cheng-Chu Zeng. "Electrochemical analysis of the triarylimidazole-type organic redox catalysts: Chemical stability and homogeneous electron transfer kinetics for the oxidation of 4-methoxybenzyl alcohol." Electrochimica Acta 199 (May 2016): 357–65. http://dx.doi.org/10.1016/j.electacta.2016.02.132.

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39

Brune, Iris, Anke Becker, Daniel Paarmann, et al. "Under the influence of the active deodorant ingredient 4-hydroxy-3-methoxybenzyl alcohol, the skin bacterium Corynebacterium jeikeium moderately responds with differential gene expression." Journal of Biotechnology 127, no. 1 (2006): 21–33. http://dx.doi.org/10.1016/j.jbiotec.2006.06.011.

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40

Lu, Nan-ning, Seung Joon Yoo, Long-Ji Li, Cheng-Chu Zeng, and R. Daniel Little. "A comparative study of organic electron transfer redox mediators: electron transfer kinetics for triarylimidazole and triarylamine mediators in the oxidation of 4-methoxybenzyl alcohol." Electrochimica Acta 142 (October 2014): 254–60. http://dx.doi.org/10.1016/j.electacta.2014.07.105.

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41

Ravikumar, Krishnan, Balasubramanian Sridhar, Jagadeesh Babu Nanubolu, Tamilselvan Rajasekaran та Basi Venkata Subba Reddy. "Four oxoindole-linked α-alkoxy-β-amino acid derivatives". Acta Crystallographica Section C Structural Chemistry 71, № 4 (2015): 322–29. http://dx.doi.org/10.1107/s2053229615005604.

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Four structures of oxoindolyl α-hydroxy-β-amino acid derivatives, namely, methyl 2-{3-[(tert-butoxycarbonyl)amino]-1-methyl-2-oxoindolin-3-yl}-2-methoxy-2-phenylacetate, C24H28N2O6, (I), methyl 2-{3-[(tert-butoxycarbonyl)amino]-1-methyl-2-oxoindolin-3-yl}-2-ethoxy-2-phenylacetate, C25H30N2O6, (II), methyl 2-{3-[(tert-butoxycarbonyl)amino]-1-methyl-2-oxoindolin-3-yl}-2-[(4-methoxybenzyl)oxy]-2-phenylacetate, C31H34N2O7, (III), and methyl 2-[(anthracen-9-yl)methoxy]-2-{3-[(tert-butoxycarbonyl)amino]-1-methyl-2-oxoindolin-3-yl}-2-phenylacetate, C38H36N2O6, (IV), have been determined. The diastere

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Tamano, Haruna, Yukina Shakushi, Mitsugu Watanabe, et al. "Preventive Effect of 3,5-dihydroxy-4-methoxybenzyl Alcohol (DHMBA) and Zinc, Components of the Pacific Oyster Crassostrea gigas, on Glutamatergic Neuron Activity in the Hippocampus." Biological Bulletin 229, no. 3 (2015): 282–88. http://dx.doi.org/10.1086/bblv229n3p282.

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Yamaguchi, Masayoshi, Kenji Yosiike, Hideaki Watanabe, and Mitsugu Watanabe. "The marine factor 3,5-dihydroxy-4-methoxybenzyl alcohol suppresses growth, migration and invasion and stimulates death of metastatic human prostate cancer cells: targeting diverse signaling processes." Anti-Cancer Drugs 33, no. 5 (2022): 424–36. http://dx.doi.org/10.1097/cad.0000000000001306.

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Wimmer, Zdeněk, Miloš Buděšínský, Tomáš Macek, et al. "Biotransformation of 2-(4-methoxybenzyl)-1-cyclohexanone by means of Saccharomyces cerevisiae." Collection of Czechoslovak Chemical Communications 52, no. 9 (1987): 2326–37. http://dx.doi.org/10.1135/cccc19872326.

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Biotransformation reduction of 2-(4-methoxybenzyl)-1-cyclohexanone was investigated. A method was elaborated for the preparation of some diastereoisomeric alcohols derived from the racemic title ketone and for the determination of the products obtained. The study resulted in the synthesis of cis-(1S,2S)-(+)-2-(4-methoxybenzyl)-1-cyclohexanol and trans-(1S,2R)-(+)-2-(4-methoxybenzyl)-1-cyclohexanol in optical purity of at least 91.6 ± 1.0% and 97.5 ± 1.0%, respectively.

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Baciocchi, Enrico, Massimo Bietti, Gianfranco Ercolani, and Steen Steenken. "−OH-Induced shift from carbon to oxygen acidity in the side-chain deprotonation of 2-, 3- and 4-methoxybenzyl alcohol radical cations in aqueous solution: results from pulse radiolysis and DFT calculations." Tetrahedron 59, no. 5 (2003): 613–18. http://dx.doi.org/10.1016/s0040-4020(02)01585-5.

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Ranchella, Michele, Cesare Rol, and Giovanni V. Sebastiani. "The Photoelectrochemical Oxidation of Benzyl Derivatives at Ti/TiO2 Anodes. A Mechanistic Approach Through Current Efficiency and Density Measurements." Journal of Chemical Research 2002, no. 5 (2002): 239–41. http://dx.doi.org/10.3184/030823402103171825.

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The mechanism of the photoelectrochemical sensitised oxidation of 4- and 3-methoxybenzyl alcohols and silanes at Ti/TiO2 ‘anatase’ and ‘rutile’ photoanodes has been investigated through current efficiency and density measurements.

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Carlsen, Per H. J. "Benzylation of alcohols and phenols with N-(4-methoxybenzyl)-o-benzenedisulfonimide." Tetrahedron Letters 39, no. 13 (1998): 1799–802. http://dx.doi.org/10.1016/s0040-4039(98)00091-4.

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CARLSEN, P. H. J. "ChemInform Abstract: Benzylation of Alcohols and Phenols with N-(4-Methoxybenzyl)-o-benzenedisulfonimide." ChemInform 29, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.199825084.

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Srikrishna, A., R. Viswajanani, J. A. Sattigeri, and D. Vijaykumar. "A new, convenient reductive procedure for the deprotection of 4-methoxybenzyl (MPM) ethers to alcohols." Journal of Organic Chemistry 60, no. 18 (1995): 5961–62. http://dx.doi.org/10.1021/jo00123a038.

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Baciocchi, Enrico, Massimo Bietti, Marina I. Ferrero, et al. "Photo-oxidative Fragmentation of Some alpha-Alkyl Substituted 4-Methoxybenzyl Alcohols and Methyl Ethers Sensitized by TiO2." Acta Chemica Scandinavica 52 (1998): 160–64. http://dx.doi.org/10.3891/acta.chem.scand.52-0160.

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