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Journal articles on the topic 'Aminobenzyl alcohol'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Zhang, Shanshan, Zheng Wang, Qianrong Cao, et al. "Aza-crown compounds synthesised by the self-condensation of 2-amino-benzyl alcohol over a pincer ruthenium catalyst and applied in the transfer hydrogenation of ketones." Dalton Transactions 49, no. 44 (2020): 15821–27. http://dx.doi.org/10.1039/d0dt03257c.

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2

Wang, Shuang, Chonggao Liu, Heng Zhou, Chengqiang Gao, and Wangqing Zhang. "An efficient route to synthesize thermoresponsive molecular bottlebrushes of poly[o-aminobenzyl alcohol-graft-poly(N-isopropylacrylamide)]." Polymer Chemistry 8, no. 12 (2017): 1932–42. http://dx.doi.org/10.1039/c6py02188c.

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The thermoresponsive molecular bottlebrushes of poly[o-aminobenzyl alcohol-graft-poly(N-isopropylacrylamide)] [P(oABA-g-PNIPAM)] were synthesized and their characteristic thermoresponse was demonstrated.

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3

Xu, Jingxiu, Qingmao Chen, Zhigao Luo, Xiaodong Tang, and Jinwu Zhao. "N-Heterocyclic carbene copper catalyzed quinoline synthesis from 2-aminobenzyl alcohols and ketones using DMSO as an oxidant at room temperature." RSC Advances 9, no. 49 (2019): 28764–67. http://dx.doi.org/10.1039/c9ra04926f.

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A facile and practical process for the synthesis of quinolines through an N-heterocyclic carbene copper catalyzed indirect Friedländer reaction from 2-aminobenzyl alcohol and aryl ketones using DMSO as an oxidant at room temperature is reported.

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4

Arcadi, Antonio, Andrea Calcaterra, Giancarlo Fabrizi, et al. "One-pot synthesis of dihydroquinolones by sequential reactions of o-aminobenzyl alcohol derivatives with Meldrum's acids." Organic & Biomolecular Chemistry 20, no. 15 (2022): 3160–73. http://dx.doi.org/10.1039/d2ob00289b.

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The functionalized 3,4-dihydroquinolin-2-one nucleus has been assembled in good to high yields through the sequential reaction of readily available N-Ts-o-aminobenzyl alcohols with Meldrum's acid derivatives under mild basic conditions.

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5

P., L. MAJUMDER, and K. SARKAR A. "Model Synthetic Studies for the Construction of 5H-Phenanthro[ 4,5-bcd]pyran and pyrone Systems." Journal Of Indian Chemical Society Vol. 66, Aug-Oct 1989 (1989): 673–80. https://doi.org/10.5281/zenodo.6024165.

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Department of Chemistry, University College of Science, 92 Acharya Prafulla Chandra Road, Calcutta -700 009 Model synthetic studies for the construction of SH-pbenanthro[ 4,5-<em>bcd</em>]pyran aod pyrone skeletal systems present in a number of oxygen heterocycles isolated from a series of Indian orchids have been carried out. The synthetic route used for the purpose involved the initial construction of dibenz[<em>bd</em>]pyran and pyrone systems with an appropriately substituted suitable two-carbon handle, which on cyclisatfon afforded the corresponding 5<em>H</em>-phenanthro[4,5-<em>bcd

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6

Manila, R. D. Kaushik, Sandhya Sharma, Jaspal Singh, and Neha Bhatt. "OXIDATION OF ORTHO AMINOBENZYL ALCOHOL: A CONCISE KINETIC STUDY." Rasayan Journal of Chemistry, Special (2021): 98–109. http://dx.doi.org/10.31788/rjc.2021.1456566.

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7

WATANABE, Takaho, Chang Qing LIN, Yoshihiro YOSHIMURA, Katsumi UCHIYAMA, Keiko OHSAWA, and Kazuo IMAEDA. "Colorimetric Determination of Chlorine Dioxide with m-Aminobenzyl Alcohol." Analytical Sciences 10, no. 1 (1994): 35–38. http://dx.doi.org/10.2116/analsci.10.35.

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8

Gataullin, R. R., and I. B. Abdrakhmanov. "Synthesis of derivatives of o-aminoacetophenone and o-aminobenzyl alcohol." Russian Journal of Organic Chemistry 43, no. 5 (2007): 723–28. http://dx.doi.org/10.1134/s1070428007050132.

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9

Aitken, R. Alan, Lewis Davidson, and Alexandra M. Z. Slawin. "The X-ray Structure of 4-Aminobenzyl alcohol (4-Aminophenylmethanol)." Journal of Chemical Crystallography 50, no. 1 (2018): 8–13. http://dx.doi.org/10.1007/s10870-018-0748-9.

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10

Arya, Anju, Akhil Mahajan, and Tejpal Singh Chundawat. "Microwave-assisted One-pot Synthesis of 2-Substituted Quinolines by Using Palladium Nanoparticles as a Catalyst developed from Green Alga Botryococcus braunii." Current Organocatalysis 7, no. 2 (2020): 82–88. http://dx.doi.org/10.2174/2213337206666190625112833.

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Background: Quinoline is a type of N-based organic heterocyclic biologically active compound. Quinolines have grasped the interest of scientists because of their wide scope of applications. Several methods have been developed for the synthesis of quinoline and its derivatives. In this study, a new, efficient, simple, one-pot synthesis of the substituted quinolines was developed by using palladium nanoparticles as a catalyst. Methods: Catalyst synthesized by algal extract of green alga Botryococcus braunii and palladium acetate solution, and characterized by different instrumental techniques li

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11

Sundaraganesan, N., H. Saleem, and S. Mohan. "Vibrational spectra, assignments and normal coordinate analysis of 3-aminobenzyl alcohol." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 59, no. 11 (2003): 2511–17. http://dx.doi.org/10.1016/s1386-1425(03)00037-4.

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12

Kiren, Yuko, Jun Deguchi, Yusuke Hirasawa, Hiroshi Morita, and Bambang Prajogo. "Justidrusamides A–D, new 2-aminobenzyl alcohol derivatives from Justicia gendarussa." Journal of Natural Medicines 68, no. 4 (2014): 754–58. http://dx.doi.org/10.1007/s11418-014-0862-8.

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13

Dixon, Wendy J., and Frank Hibbert. "Formation of a cyclic tetrahedral intermediate by the addition of water to 2-methyl-4H- 3,1-benzoxazine followed by ring opening to 2-aminobenzyl acetate and 2-acetylaminobenzyl alcohol; pH-dependence of rate of reaction and product ratio." Canadian Journal of Chemistry 77, no. 5-6 (1999): 1035–41. http://dx.doi.org/10.1139/v99-091.

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Kinetic studies have shown that addition of water to protonated 2-methyl-4H-3,1-benzoxazine occurs to give a cyclic tetrahedral carbonyl addition intermediate. At pH <5, the intermediate is protonated and reacts to 2-aminobenzyl acetate, whereas at pH >7.5, the unprotonated intermediate collapses to give 2-acetylaminobenzyl alcohol. The former reaction is catalysed by buffer base but the latter is uncatalysed. At pH 9-12, reaction of hydroxide ion with protonated 2-methyl-4H-3,1-benzoxazine to give 2-acetylaminobenzyl alcohol becomes important, and at pH >12, the same product is forme

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14

Cho, Chan Sik, Bok Tae Kim, Heung-Jin Choi, Tae-Jeong Kim, and Sang Chul Shim. "Ruthenium-catalyzed oxidative coupling and cyclization between 2-aminobenzyl alcohol and secondary alcohols leading to quinolines." Tetrahedron 59, no. 40 (2003): 7997–8002. http://dx.doi.org/10.1016/j.tet.2003.08.027.

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15

Malone, Vincent F., Amy J. Chastain, John T. Ohlsson, Loelle S. Poneleit, Michele Nemecek-Marshall, and Ray Fall. "Characterization of a Pseudomonas putidaAllylic Alcohol Dehydrogenase Induced by Growth on 2-Methyl-3-Buten-2-ol." Applied and Environmental Microbiology 65, no. 6 (1999): 2622–30. http://dx.doi.org/10.1128/aem.65.6.2622-2630.1999.

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ABSTRACT We have been working to develop an enzymatic assay for the alcohol 2-methyl-3-buten-2-ol (232-MB), which is produced and emitted by certain pines. To this end we have isolated the soil bacteriumPseudomonas putida MB-1, which uses 232-MB as a sole carbon source. Strain MB-1 contains inducible 3-methyl-2-buten-1-ol (321-MB) and 3-methyl-2-buten-1-al dehydrogenases, suggesting that 232-MB is metabolized by isomerization to 321-MB followed by oxidation. 321-MB dehydrogenase was purified to near-homogeneity and found to be a tetramer (151 kDa) with a subunit mass of 37,700 Da. It catalyzes

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16

Barham, Ahmad S. "Influence of pH on the Electropolymerisation of 2-Aminophenol and 2-Aminobenzyl Alcohol." Journal of New Materials for Electrochemical Systems 18, no. 1 (2015): 037–41. http://dx.doi.org/10.14447/jnmes.v18i1.387.

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The electrochemical oxidation and polymerisation of 2-aminophenol and 2-aminobenzyl alcohol in aqueous solutions of different pH values has been studied. Polymer films of the studied monomers on gold electrodes were synthesized. The behaviour of both monomers is quite different, illustrating the resonance effect of the hydroxyl group being bound directly to the benzene ring for 2-aminophenol. For each compound it is shown that oxidation in acidic solutions is most difficult due to the protonation of the amine group. These polymer films can be used for applications such as corrosion protection

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17

Lei, Xiping, and Zhixing Su. "Synthesis and properties of the copolymers based on aniline and 2-aminobenzyl alcohol." Journal of Polymer Research 15, no. 5 (2008): 421–26. http://dx.doi.org/10.1007/s10965-008-9187-1.

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18

Nguyen, My T., and Arthur F. Diaz. "Water-Soluble Conducting Copolymers of o-Aminobenzyl Alcohol and Diphenylamine-4-sulfonic Acid." Macromolecules 27, no. 23 (1994): 7003–5. http://dx.doi.org/10.1021/ma00101a048.

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19

Kubo, Hajime, Kota Nishiyama, Tomohide Sato, Kimio Higashiyama, and Shigeru Ohmiya. "Facile in situ Preparation of o-Azaxylylene from N,O-Diethoxycarbonyl-o-aminobenzyl Alcohol." HETEROCYCLES 48, no. 6 (1998): 1103. http://dx.doi.org/10.3987/com-98-8135.

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20

Cho, Chan Sik, Bok Tae Kim, Tae-Jeong Kim, and Sang Chul Shim. "Ruthenium-catalysed oxidative cyclisation of 2-aminobenzyl alcohol with ketones: modified Friedlaender quinoline synthesis." Chemical Communications, no. 24 (December 10, 2001): 2576–77. http://dx.doi.org/10.1039/b109245f.

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21

Seeman, Jeffrey I., Henry V. Secor, Hoong Sun Im, and E. R. Bernstein. "Spectroscopic observation of individual sp3-nitrogen stereoisomers. Supersonic jet studies of 2-aminobenzyl alcohol." Journal of the American Chemical Society 112, no. 19 (1990): 7073–74. http://dx.doi.org/10.1021/ja00175a059.

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22

Chan, H. S. O., S. C. Ng, W. S. Sim, S. H. Seow, K. L. Tan, and B. T. G. Tan. "Synthesis and characterization of conducting poly(o-aminobenzyl alcohol) and its copolymers with aniline." Macromolecules 26, no. 1 (1993): 144–50. http://dx.doi.org/10.1021/ma00053a022.

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23

Kinzhalov, M. A., G. L. Starova, M. Haukka, and V. P. Boyarskii. "Reaction of o-aminophenol and o-aminobenzyl alcohol with palladium(II) bis(isocyanide) complexes." Russian Journal of General Chemistry 86, no. 10 (2016): 2350–55. http://dx.doi.org/10.1134/s1070363216100170.

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24

Sundaraganesan, N., H. Saleem, S. Mohan, and M. Ramalingam. "FT-Raman and FTIR spectra, assignments and ab initio calculations of 2-aminobenzyl alcohol." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 61, no. 3 (2005): 377–85. http://dx.doi.org/10.1016/j.saa.2004.04.012.

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25

Chism, John P., and Douglas E. Rickert. "In vitro activation of 2-aminobenzyl alcohol and 2-amino-6-nitrobenzyl alcohol, metabolites of 2-nitrotoluene and 2,6-dinitrotoluene." Chemical Research in Toxicology 2, no. 3 (1989): 150–56. http://dx.doi.org/10.1021/tx00009a005.

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26

Müller, Ivonne A., Felix Kratz, Manfred Jung, and André Warnecke. "Schiff bases derived from p-aminobenzyl alcohol as trigger groups for pH-dependent prodrug activation." Tetrahedron Letters 51, no. 33 (2010): 4371–74. http://dx.doi.org/10.1016/j.tetlet.2010.06.055.

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27

Hua, Fengjun, and Eli Ruckenstein. "Highly soluble conducting poly(ethylene oxide) grafted at two sites of poly(o-aminobenzyl alcohol)." Journal of Polymer Science Part A: Polymer Chemistry 42, no. 19 (2004): 4756–64. http://dx.doi.org/10.1002/pola.20323.

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28

Cho, Chan Sik, Bok Tae Kim, Tae-Jeong Kim, and Sang Chul Shim. "ChemInform Abstract: Ruthenium-Catalyzed Oxidative Cyclization of 2-Aminobenzyl Alcohol with Ketones: Modified Friedlaender Quinoline Synthesis." ChemInform 33, no. 16 (2010): no. http://dx.doi.org/10.1002/chin.200216148.

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29

NISHIYAMA, K., H. KUBO, T. SATO, K. HIGASHIYAMA, and S. OHMIYA. "ChemInform Abstract: Facile in situ Preparation of o-Azaxylylene from N,O-Diethoxycarbonyl-o-aminobenzyl Alcohol." ChemInform 29, no. 39 (2010): no. http://dx.doi.org/10.1002/chin.199839068.

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30

Barham, Ahmad S. "Electrochemical studies of 3-aminophenol and 3-aminobenzyl Alcohol in Aqueous Solutions at Different pH Values." International Journal of Electrochemical Science 10, no. 6 (2015): 4742–51. http://dx.doi.org/10.1016/s1452-3981(23)06661-0.

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31

Sundaraganesan, N., B. Anand, C. Meganathan, B. Dominic Joshua, and H. Saleem. "Vibrational spectra and assignments of 3-aminobenzyl alcohol by ab initio Hartree–Fock and density functional method." Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 69, no. 1 (2008): 198–204. http://dx.doi.org/10.1016/j.saa.2007.03.031.

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32

Zhang, Xiaopeng, Ping Wang, Xueli Niu, Zhengwei Li, Xuesen Fan, and Guisheng Zhang. "Selenium-catalyzed oxidative carbonylation of 2-aminobenzyl alcohol to give 1,4-dihydro-2 H -3,1-benzoxazin-2-one." Chinese Journal of Catalysis 37, no. 11 (2016): 2034–38. http://dx.doi.org/10.1016/s1872-2067(16)62537-8.

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33

B. Masesane, I., E. Muriithi, and T. H. Tabane. "Simple grinding-induced reactions of 2-aminobenzyl alcohol and benzaldehyde derivatives, a rapid synthetic route to 3,1-benzoxazines." Bulletin of the Chemical Society of Ethiopia 28, no. 2 (2014): 301. http://dx.doi.org/10.4314/bcse.v28i2.14.

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34

Cho, Chan Sik, Hyo Jin Seok, and Sang Oral Shim. "A rhodium-catalyzed route for oxidative coupling and cyclization of 2-aminobenzyl alcohol with ketones leading to quinolines." Journal of Heterocyclic Chemistry 42, no. 6 (2005): 1219–22. http://dx.doi.org/10.1002/jhet.5570420630.

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35

Ozyilmaz, Ali Tuncay, Cumali Celik, and Begum Ozgen. "Nanoparticle and Schiff Base Compound in Poly(O-Aminobenzyl Alcohol) Coating for Protection of 316L Stainless Steel against Corrosion." Journal of Nano Research 75 (September 21, 2022): 99–119. http://dx.doi.org/10.4028/p-xe202d.

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The electrochemical synthesis of poly (o-aminobenzyl alcohol) (PABA) coatings containing three different amounts of NiZnFe4O4 nanoparticle (NP) with and without 0.25 mM Schiff base (ORG) on stainless steel (SS) was carried out in 0.15 M LiClO4 containing acetonitrile (ACN) solution. The synthesis curves of PABA-NP and PABA-ORG-NP films exhibited the different current and monomer oxidation potential values indicating the presence of NP and ORG compounds. Besides, the addition of ORG to the NP-containing synthesis solution resulted in an increase in the electropolymerization rate of the PABA fil

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36

Slabko, O. Yu, A. V. Kachanov, and V. A. Kaminskii. "Reactions of 1,5-diketones with 2-aminobenzyl alcohol and 2-aminomethylaniline and behavior of the products in oxidative coupling." Russian Journal of Organic Chemistry 48, no. 9 (2012): 1180–86. http://dx.doi.org/10.1134/s1070428012090059.

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37

Salehi, Mehdi, and Maryam Hasanzadeh. "Characterization, crystal structures, electrochemical and antibacterial studies of four new binuclear cobalt(III) complexes derived from o-aminobenzyl alcohol." Inorganica Chimica Acta 426 (February 2015): 6–14. http://dx.doi.org/10.1016/j.ica.2014.10.023.

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38

BHATTACHARYYA, S. "ChemInform Abstract: Facile Two-Step Synthesis of 2-((2′-Aminobenzyl)amino)benzyl Alcohol, a Naturally Occurring Amine from Justicia gendarussa." ChemInform 27, no. 6 (2010): no. http://dx.doi.org/10.1002/chin.199606277.

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39

Slabko, O. Yu, A. V. Kachanov, and V. A. Kaminskii. "ChemInform Abstract: Reactions of 1,5-Diketones with 2-Aminobenzyl Alcohol and 2-Aminomethylaniline and Behavior of the Products in Oxidative Coupling." ChemInform 44, no. 10 (2013): no. http://dx.doi.org/10.1002/chin.201310185.

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40

Vilà, Anna, Alberto Gómez-Núñez, Xavier Alcobé, Sergi Palacios, Teo Puig Walz, and Concepción López. "Influence of the Nature of Aminoalcohol on ZnO Films Formed by Sol-Gel Methods." Nanomaterials 13, no. 6 (2023): 1057. http://dx.doi.org/10.3390/nano13061057.

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Here we present comparative studies of: (i) the formation of ZnO thin films via the sol-gel method using zinc acetate dihydrate (ZAD), 2-methoxyethanol (ME) as solvent, and the aminoalcohols (AA): ethanolamine, (S)-(+)-2-amino-1-propanol, (S)-(+)-2-amino-3-methyl-1-butanol, 2-aminophenol, and aminobenzyl alcohol, and (ii) elemental analyses, infrared spectroscopy, X-ray diffraction, scanning electron microscopy, absorption and emission spectra of films obtained after deposition by drop coating on glass surface, and thermal treatments at 300, 400, 500 and 600 °C. The results obtained provide co

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41

Das, Kalicharan, Avijit Mondal, Debjyoti Pal, and Dipankar Srimani. "Sustainable Synthesis of Quinazoline and 2-Aminoquinoline via Dehydrogenative Coupling of 2-Aminobenzyl Alcohol and Nitrile Catalyzed by Phosphine-Free Manganese Pincer Complex." Organic Letters 21, no. 9 (2019): 3223–27. http://dx.doi.org/10.1021/acs.orglett.9b00939.

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42

Li, Daojin, Tianyong Tu, and Xiuyuan Wu. "Efficient preparation of template immobilization-based boronate affinity surface-imprinted silica nanoparticles using poly(4-aminobenzyl alcohol) as an imprinting coating for glycoprotein recognition." Analytical Methods 10, no. 36 (2018): 4419–29. http://dx.doi.org/10.1039/c8ay00632f.

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43

Motokura, Ken, Tomoo Mizugaki, Kohki Ebitani, and Kiyotomi Kaneda. "Multifunctional catalysis of a ruthenium-grafted hydrotalcite: one-pot synthesis of quinolines from 2-aminobenzyl alcohol and various carbonyl compounds via aerobic oxidation and aldol reaction." Tetrahedron Letters 45, no. 31 (2004): 6029–32. http://dx.doi.org/10.1016/j.tetlet.2004.06.023.

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44

Nath, Mala, and Rakesh Yadav. "Synthesis, Spectral and Thermal Studies of Fe(III), Co(II), Ni(II), Cu(II) and Zn(II) Complexes of Schiff Bases Derived from o-Aminobenzyl Alcohol." Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry 25, no. 9 (1995): 1529–47. http://dx.doi.org/10.1080/15533179508218288.

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45

Syamal, A., and M. M. Singh. "Syntheses and characterization of new cobalt(II) complexes of polystyrene-supported resin containing the Schiff bases derived from 3-formylsalicylic acid and 2-aminophenol, 2-aminobenzyl alcohol or 2-hydroxybenzylamine." Reactive Polymers 21, no. 1-2 (1993): 45–52. http://dx.doi.org/10.1016/0923-1137(93)90053-i.

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46

Gopalaiah, Kovuru, Anupama Saini, and Alka Devi. "Iron-catalyzed cascade reaction of 2-aminobenzyl alcohols with benzylamines: synthesis of quinazolines by trapping of ammonia." Organic & Biomolecular Chemistry 15, no. 27 (2017): 5781–89. http://dx.doi.org/10.1039/c7ob01159h.

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47

Yang, Cheng, and Peter Wan. "Photosolvolysis of 2-aminobenzl alcohol in aqueous solution." Journal of Photochemistry and Photobiology A: Chemistry 80, no. 1-3 (1994): 227–32. http://dx.doi.org/10.1016/1010-6030(94)85005-4.

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48

Yu, X., W. Yao, W. Hu, and D. Wang. "Iridium-catalyzed synthesis of quinolines from 2-aminobenzyl alcohols with secondary alcohols." Russian Journal of General Chemistry 86, no. 2 (2016): 376–79. http://dx.doi.org/10.1134/s1070363216020298.

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49

Halstian, A. H., A. S. Вushuiev, and Ye Yu Vasylenko. "Ozonation of 4-aminotoluene as a new method of synthesis of 4-aminobenzaldehyde – an intermediate for the production of anti-tuberculosis drugs." Current issues in pharmacy and medicine: science and practice 15, no. 1 (2022): 13–18. http://dx.doi.org/10.14739/2409-2932.2022.1.249620.

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Solutizon is an original anti-TB drug that is effective in resisting mycobacteria to other anti-TB drugs, which is obtained by the interaction of thiosemicarbazone 4-aminobenzaldehyde and sodium oxymethylene sulfonate. 4-Aminobenzaldehyde is synthesized by redox conversion of 4-nitrotoluene in the presence of sodium polysulfide. The reaction is carried out in boiling alcohol, and 4-aminobenzaldehyde is separated after steam distillation with a yield of 40–50 %. However, today this method loses its practical, environmental and economic attractiveness, as it has significant disadvantages – low p

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50

Horák, Václav, Yonco Mermersky, and Dalal B. Guirguis. "3,5-Di-tert-butyl-1,2-benzoquinone Cleaves a CC-bond in Vicinal Aminobenzyl Alcohols." Collection of Czechoslovak Chemical Communications 59, no. 1 (1994): 227–30. http://dx.doi.org/10.1135/cccc19940227.

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Two vicinal aminobenzyl alcohols, L-threo-1-(4-methylthiophenyl)-2-amino-1,3-propanediol (IIa) and 1-phenyl-2-amino-1,3-propanediol (IIb), underwent, under mild conditions, CC-bond cleavage with 3,5-di-tert-butyl-1,2-benzoquinone (I) producing in high yields 4-methylthiobenzaldehyde (Va) and benzaldehyde (Vb), respectively, and 2-hydroxymethyl-4,6-di-tert-butylbenzoxazole (VII). Ethanolamine (VIII) under identical conditions produced benzoxazole VII. The reported reaction is a second case in which quinone I mimics reactions of pyridoxal.

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