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Relevant bibliographies by topics / Benzyloxy

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Academic literature on the topic 'Benzyloxy'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 July 2025

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Journal articles on the topic "Benzyloxy"

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Penov-Gasi, Katarina, Ksenija Kuhajda, Stanko Cvjeticanin, et al. "Synthesis of some diol DErivatives as potential reagents in steroid chemistry." Acta Periodica Technologica, no. 34 (2003): 111–18. http://dx.doi.org/10.2298/apt0334111p.

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The multistage syntheses of the p-toluenesulphonyloxy esters (1-benzyloxy-4-p-toluenesulphonyloxybutane (3a) 1-benzyloxy-6-p-toluenesulphonyloxyhexane (3b) and 1-benzyloxy-10-p-toluenesulphonyloxydecane (3c)(, alkyl chlorides (1-benzyloxy-4-chlorobutane (4a), 1-benzyloxy-6-chlorohexane (4b) and 1-benzyloxy-10-chlorodecane (4c)(, as well as alkyl iodides (1-benzyloxy-4-iodobutane (5a), 1-benzyloxy-6-iodohexane (5b) and 1-benzyloxy-10-iododecane (5c)( with the terminal O-benzyl groups starting from 1,4-butanediol (1a), 1,6-hexanediol (1b) and 1,10-decanediol (1c) were carried out. The possibilit

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Peng, Wan Xi, Lan Sheng Wang, Qing Ding Wu, and Shi Long Xiang. "Analysis on Health Risk of Volatile Organic Compounds of Poplar Composite Biomaterial by GC-MS." Advanced Materials Research 129-131 (August 2010): 60–64. http://dx.doi.org/10.4028/www.scientific.net/amr.129-131.60.

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Poplar composite biomaterial, which self bonded under high temperature and pressure, is a new indoors materials. In order to evaluate its potential health risk to human settlements, the volatile organic compounds of poplar composite biomaterial were adsorbed and determined by TD-GC-MS. The result were: (1) The main constituents of volatiles at 40°С were acetic acid(50.6%), 1,2-benzenedicarboxylic acid, mono(2-ethylhexyl) ester(8.48%), [1,1':3',1''-terphenyl]-2'-ol(3.98%), 1,2-propanediol, 3-benzyloxy-1,2-d iacetyl-(3.12%), etc. (2) The main constituents of volatiles at 60°С were acetic acid(46

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Tang, Zheng-Hua, Yu Tang, and Xiao-Ping Cao. "N-Benzyl-2-[3,5-bis(benzyloxy)benzyloxy]benzamide." Acta Crystallographica Section E Structure Reports Online 63, no. 7 (2007): o3283. http://dx.doi.org/10.1107/s1600536807029406.

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Huc, Vincent, Eloïne Npetgat, Vincent Guérineau, et al. "p-(Benzyloxy)calix[8]arene Synthesis Revisited: p-(Benzyloxy)calix[4]-, p-(Benzyloxy)calix[5]-, p-(Benzyloxy)calix[7]-, and p-(Benzyloxy)bis(homooxa)calix[4]arenes." European Journal of Organic Chemistry 2010, no. 32 (2010): 6186–92. http://dx.doi.org/10.1002/ejoc.200901405.

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Khurana, Nikhil, Pankaj Sharma, Sunita Bhagat, and Suman Bala Sharma. "Effect of a novel succinamic acid derivative as potential anti-diabetic agent in experimental diabetic rats." Journal of Drug Delivery and Therapeutics 8, no. 6-s (2018): 57–62. http://dx.doi.org/10.22270/jddt.v8i6-s.2080.

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4-((benzyloxy) amino)-2-hydroxy-4-oxobutanoic acid which is a succinamic acid derivative has been synthesized in 3 step reaction with malic acid. Its structure confirmation was done by various techniques like 1H NMR, 13C NMR, & HRMS and is recently proposed as an insulinotropic agent for the treatment of non-insulin dependent diabetes mellitus. In the present study, the effect of 4-((benzyloxy) amino)-2-hydroxy-4-oxobutanoic acid on plasma glucose, serum insulin, serum lipid profile and lipid peroxidation in streptozotocin–nicotinamide induced type 2 diabetic model was investigated. 4-((be

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Martis, Alberto, Alberto Luridiana, Angelo Frongia, et al. "Acid-catalyzed reaction of 2-hydroxycyclobutanone with benzylic alcohols." Organic & Biomolecular Chemistry 15, no. 47 (2017): 10053–63. http://dx.doi.org/10.1039/c7ob02545a.

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Hřebabecký, Hubert, Milena Masojídková, and Antonín Holý. "Synthesis of Purine Nucleoside Analogues Derived from Carbocyclic 5-C-(Hydroxymethyl)hexopyranoses." Collection of Czechoslovak Chemical Communications 69, no. 2 (2004): 435–52. http://dx.doi.org/10.1135/cccc20040435.

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(1R,2R,3R,4S)-3-(Benzyloxy)-5,5-bis(hydroxymethyl)cyclohexane-1,2,4-triol (1) was converted to (3aS,4R,5S,7aR)-4-(benzyloxy)-2-oxo-6,6-bis[(trityloxy)methyl]hexahydro-2λ4-1,3,2-benzodioxathiol-5-ol (3) and subsequently to (3aS,4R,5S,7aR)-4-(benzyloxy)-2,2-dioxo-6,6-bis[(trityloxy)methyl]hexahydro-2λ4-1,3,2-benzodioxathiol-5-yl benzoate (4). Treatment of sulfate 4 with adenine and DBU afforded, after deprotection, 7 and 22 in low yields. Reaction of sulfite 3 with lithium azide gave (1R,2R,3S,6S)-6-azido-2-(benzyloxy)-4,4-bis[(trityloxy)methyl]-cyclohexane-1,3-diol (10) and (1S,4R,5S,6S)-5-azid

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Salamci, Emine, and Ayse Kilic Lafzi. "Efficient synthesis of aziridinecyclooctanediol and 3-aminocyclooctanetriol." Beilstein Journal of Organic Chemistry 18 (November 11, 2022): 1539–43. http://dx.doi.org/10.3762/bjoc.18.163.

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Cyclooctene endoperoxide was used as the key compound for the synthesis of aziridinecyclooctanediol and 3-aminocyclooctanetriol. Reduction of the cyclooctene endoperoxide, prepared by photooxygenation of cis,cis-1,3-cyclooctadiene, with zinc gave a cyclooctenediol and then benzylation of the hydroxy group yielded dibenzylated cyclooctene. Oxidation of the latter compound by OsO4/NMO followed by mesylation of the hydroxy group provided bis(benzyloxy)cyclooctane-1,2-diyl dimethanesulfonate. Reaction of the bis(benzyloxy)cyclooctane-1,2-diyl dimethanesulfonate with NaN3 gave 2-azido-3,8-bis(benzy

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Jovanovic-Santa, Suzana, Sanja Gaborov, and Julijana Petrovic. "Synthesis of 3-benzyloxyl-17-maleyloxy-16, 17-secoestra- 1, 3, 5 (10)-triene-16-nitrile - Sinteza 3-benziloksi-17-maleiloksi- 16, 17-sekoestra-1, 3, 5 (10)-trien-16-nitrila." Zbornik Matice srpske za prirodne nauke, no. 103 (2002): 5–9. http://dx.doi.org/10.2298/zmspn0201005j.

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Under the conditions of Beckmann fragmentation reaction 3-benzyloxy-17(-hydroxyestra-1, 3, 5, (10)-triene-16-one oxime (2) gave the D-seco derivative 3. Sodium borohydride reduction of this compound afforded 3-benzyloxy-17-hydroxy-16, 17-secoestra-1, 3, 5 (10)-triene-16-nitrile (4). The esterification of seco-cyanoalcohol 4 was achieved by action of maleic acid anhydride in dry pyridine, yielding 3-benzyloxy-17-maleyloxy-16 17-secoestra-1, 3, 5 (10)-triene-16-nitrile (5).

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Varelis, P., and BL Johnson. "Preparation of Optically Active (S)-2-(Benzyloxy)propanal." Australian Journal of Chemistry 48, no. 10 (1995): 1775. http://dx.doi.org/10.1071/ch9951775.

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A convenient and large scale amenable preparation of optically active ethyl (S)-2-( benzyloxy )propionate (5) from ethyl (S)-lactate (4), and the conversion of the ester (5) by two alternative methods into (S)-2-( benzyloxy ) propanal (1) are described.

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Dissertations / Theses on the topic "Benzyloxy"

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Oostendorp, Ryan. "The Synthesis of Benzyloxy Substituted DP-PPVs." Wright State University / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=wright1376310240.

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Merkley, Nadine. "Carbenes and radicals from benzyloxy [delta]3-1,3,4-oxadiazolines /." *McMaster only, 2001.

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Thesis (Ph.D.) -- McMaster University, 2001.<br>[Delta] in title is a Greek letter. The number 3 in title is superscript. Includes bibliographical references (leaves 147-162). Also available via World Wide Web.

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Gastal, Françoise. "Synthèse d'alpha-N-hydroxy et benzyloxy aminoester et de leurs analogues phosphores." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb37597859m.

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Lear, Jeremy M. "The Synthesis of Benzyloxy Substituted DP-PPV and Examination of the Horner-Wadsworth-Emmons Reaction in the Synthesis of DP-PPV." Wright State University / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=wright1401459783.

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Peterson, Rebecca Anne 1973. "Characterization and optimization of ordering in thin films of 2,3,9,10,16,17,23,24-oktakis((2-benzyloxy)ethoxy)phthalocyaninato copper and its metal free analogue." Thesis, The University of Arizona, 1998. http://hdl.handle.net/10150/278681.

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The variables which control the degree of molecular ordering of CuPc(OC₂OBz)₈ and H₂Pc(OC₂OBz)₈ within Langmuir-Blodgett (LB) thin films were identified and optimized. Stabilizing the Langmuir film, lowering the subphase temperature, transferring to phenyl terminated substrates, and annealing lead to enhanced ordering. Infrared data confirms increased anisotrophy (dichroic ratio, R-4.6) and order (order parameter, S₂-6.5) within these films, and predicts a tilted elliptical orientation of the molecules. Small angle X-ray scattering data and atomic force microscopy images correlate, giving a co

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Pettersen, Jade Kristin. "Preparation and properties of self-assembled resorcinarene monolayers." Thesis, Curtin University, 2010. http://hdl.handle.net/20.500.11937/933.

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Several resorcinarene and calixarene based receptors were synthesised with the overarching aim of developing selective hydrocarbon sensors for application in the petroleum exploration industry.Thioacetyl resorcinarenes functionalised at the upper rim with methoxy, propoxy and benzyloxy groups were synthesised, along with a methylene bridged cavitand. Similar hydroxy and methoxy resorcinarenes functionalised at the lower rim with decylsulfide groups were prepared, along with a p-tert-butylcalix[4]arene thiol derivative.The receptors were allowed to self-assemble on gold substrates, and the resu

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Majzlík, Petr. "Radikálové reakce rozpadu N-H, O-H a O-O vazeb účinkem homogenních a heterogenních redox činidel." Doctoral thesis, Vysoké učení technické v Brně. Fakulta chemická, 2010. http://www.nusl.cz/ntk/nusl-233309.

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The Ph.D. thesis was focused on EPR study of redox reactions of selected types of phenols, secondary amines and diperoxy coumpounds. Within the study some redox agents were employed in nonpolar, in some special cases also in polar solvents. EPR spectra of generated radical products were interpreted using spectral simulation. Study of radical reactions under participation of phenols was preferentially concentrated on the behavior of para methyl substituted phenols, where the instability of this substituent in relation to the applied redox agents was evaluated. The tendency towards the abstracti

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Shu-Wei, Hsu, and 許書維. "Synthesis and Biological Activities of 2-Substituted Benzyloxy Benzoic Acid Derivatives." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/48608478932630792656.

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碩士<br>中國醫藥學院<br>藥物化學研究所<br>91<br>In order to obtain novel compounds with potent anti-inflammatory, anti-allergic and anti-diarrhea activities, 2-benzyloxybenzaldehyde was used as the lead compound, and 2-substituted benzyloxy benzoic acid derivatives were synthesized. 2-substituted benzyloxy benzonitriles 17-25, 2-substituted benzyloxy 2-methylbenzenes 26-29, 2-substituted benzyloxy phenyl methanols 30-33, 2-substituted benzyloxy benzoates 34-41, 2-substituted benzyloxy benzamides 42-44 and 2-substituted benzylamino benzoates 45-55 were synthesized by the benzylation with potassium

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Chung, Chuan-Chung, та 鍾權忠. "Chiral Anti-Aldol Reaction Studies and Synthetic applications ofγ-Benzyloxy Substituted Vinylogous Urethane". Thesis, 2003. http://ndltd.ncl.edu.tw/handle/2s49k8.

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碩士<br>朝陽科技大學<br>應用化學系碩士班<br>91<br>一. Chiral Anti-Aldol Reaction Studies of Chiral γ-Benzyloxy Subsituted Vinylogous Urethane Chiral γ-Benzyloxy Subsituted Vinylogous Urethane 1 was deprotonated and reacted with aldehyde to form anti-aldol product, the product selectivity was analyzed using chiral column to determine their enantioselectivity.

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Chin-Wen, Wang, and 王志文. "Synthesis of 2-(benzyloxy)benzoic acid derivatives as the inhibitor of ganglioside GM1 receptor." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/38257738085262709567.

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碩士<br>中國醫藥大學<br>藥物化學研究所<br>93<br>Structural biology studies on heat-labile enterotoxin (LT) from enterotoxigenic Escherichia coli. and the closely related cholera toxin (CT), shed light on the action mechanism of toxin at molecular and atomic levels. The B pentamer protein of the toxins recognized the receptor ganglioside GM1 presented on the gastrointestinal tract of human host and triggers endocytosis . The enzymatic A1 fragment of the toxin enters the cytosol it modifies the alpha subunit of stimulatory G protein (Gsα) and locks the G protein in its GTP-bound form, which continually stimula

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Book chapters on the topic "Benzyloxy"

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Simola, Nicola, Micaela Morelli, Tooru Mizuno, et al. "N,N Dimethyl-2[α-(o-Tolyl)Benzyloxy]Ethylamine HCl or Citrate." In Encyclopedia of Psychopharmacology. Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_4389.

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Vogl, T. J., W. Pegios, C. McMahon, et al. "Hepatobiliary Magnetic Resonance Imaging: First Experiences with Gadolinium Benzyloxy-proprionic-tetraacetic Acid." In Lebertumoren und portale Hypertension. Springer Berlin Heidelberg, 1993. http://dx.doi.org/10.1007/978-3-642-77834-6_14.

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"4′-Benzyloxy-2′-hydroxy-3,4-methylenedioxychalcone." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0535-1_1131.

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"4-Benzyloxy-2′-hydroxy-3,4′-dimethoxychalcone." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0535-1_1132.

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Balci, M., M. Çelik, and M. S. Gültekin. "Oxidative Debenzylation of Bis(benzyloxy)benzenes." In Quinones and Heteroatom Analogues. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-028-00090.

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Benneche, T. "Addition of (Benzyloxy)fluorocarbene to Acrylonitrile." In Acetals: Hal/X and O/O, S, Se, Te. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-029-00137.

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Li, W.-R. "By Reductive Cleavage of -Benzyloxy β-Lactams." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00144.

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Enna, S. J., and David B. Bylund. "4-Benzyloxy-3,5-Dimethoxy-N-[(1-Dimethylaminocyclopentyl)Methyl]Benzamide." In xPharm: The Comprehensive Pharmacology Reference. Elsevier, 2007. http://dx.doi.org/10.1016/b978-008055232-3.63431-2.

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Dell, C. P. "By Cyclization of 2-(Benzyloxy)benzaldehydes and Related Species." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00071.

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König, B. "2,3-Disubstituted Furans from 1-(Benzyloxy)-3-tosylalkenes and Aldehydes." In Fully Unsaturated Small-Ring Heterocycles and Monocyclic Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-009-00273.

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Conference papers on the topic "Benzyloxy"

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Chen, Zhenzhen, Keqin Wu, Junri Wen, Hongqin Yang, and Yiru Peng. "Photo-induced intra-molecular energy transfer of tetra-{3,5-di-(4-nitro benzyloxy) benzyloxy} zinc (II) phthalocyanine." In 3rd International Conference on Material, Mechanical and Manufacturing Engineering (IC3ME 2015). Atlantis Press, 2015. http://dx.doi.org/10.2991/ic3me-15.2015.428.

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Wang, Min, Ping Wang, Yiqiang OuYang, et al. "Synthesis of 7-(benzyloxy)-4-chloro-6-methoxyquinazoline." In 2015 International conference on Applied Science and Engineering Innovation. Atlantis Press, 2015. http://dx.doi.org/10.2991/asei-15.2015.422.

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Zhang, Tiantian, Dongdong Ma, Sujuan Pan, et al. "Photoinduced electron transfer between benzyloxy dendrimer phthalocyanine and benzoquinone." In SPIE/COS Photonics Asia, edited by Qingming Luo, Xingde Li, Ying Gu, and Yuguo Tang. SPIE, 2016. http://dx.doi.org/10.1117/12.2246314.

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Hendrickx, E., B. L. Volodin, D. D. Steele, et al. "Phase stability of guest/host photorefractive polymers studied by light scattering experiments." In Organic Thin Films for Photonic Applications. Optica Publishing Group, 1997. http://dx.doi.org/10.1364/otfa.1997.fd.4.

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In recent years, we developed plasticized guest-host photorefractive polymers with a glass transition temperature below room temperature.1 However, in these guest/host polymers a gradual crystallization of the chromophores (50% wt.) limits the shelf lifetime of the samples. The lifetime of DMNPAA(2,5-dimethyl-4-(p-nitrophenylazo) anisole) : PVK(poly-vinylcarbazole) : ECZ(N-ethylcarbazole) : TNF(tri-nitrofluorenone) samples with 50% wt. of DMNPAA was found to vary between a few hours and a few months depending on the starting materials and the processing conditions. Here we present a new guest/

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Mahajan, Aman, Mandeep Singh, Himani Gupta, R. K. Bedi, S. Kumar, and D. K. Aswal. "Characterization of alkali halides doped 1-(2-methoxy benzyloxy)-8- hydroxy-9,10-anthraquinone films for photovoltaic applications." In INDIAN VACUUM SOCIETY SYMPOSIUM ON THIN FILMS: SCIENCE AND TECHNOLOGY. AIP, 2012. http://dx.doi.org/10.1063/1.4732440.

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Khvostov, Mikhail, Darya Kuznetsova, Sergey Kuranov, et al. "Hypoglycemic activity study of novel bornyl derivatives of <em>p</em>-(benzyloxy)phenylpropionic acid." In 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07441.

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"Quantum Chemical Insights into 2-[2-(Benzyloxy)benzylidene] malononitrile: DFT Analysis, MEP Surface Mapping, and HOMO-LUMO Energies." In 4th International Conference on Engineering and Applied Natural Sciences ICEANS 2023. All Sciences Academy, 2023. http://dx.doi.org/10.59287/as-proceedings.348.

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Nikalje, Anna Pratima, Urja Nimbalkar, Julio Seijas Vázquez, and M. Pilar Vazquez-Tato. "Ultrasound assisted synthesis of 4-(benzyloxy)-N-(3-chloro-2-(substituted phenyl)-4-oxoazetidin-1-yl) benzamide ." In The 21st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04809.

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HUANG, QIANG, and BAOZHONG ZHENG. "PHASE TRANSFER CATALYTIC SYNTHESIS OF 4-BENZYLOXYL-3-METHOXYLBENZALDEHYDE-COPOLYSTYRENE RESIN." In Proceedings of the 6th International Conference on ICAMP. WORLD SCIENTIFIC, 2011. http://dx.doi.org/10.1142/9789814322799_0053.

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Reports on the topic "Benzyloxy"

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ทิพยางค์, สันติ, วรินทร ชวศิริ, ปรีชา ภูวไพรศิริศาล, พัฒทรา สวัสดี та ไพฑูรย์ รัชตะสาคร. สารสำคัญและการประกันคุณภาพอาหารเสริมจากกระชายดำ : รายงานการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2008. https://doi.org/10.58837/chula.res.2008.51.

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สารฟลาโวนอยด์ 10 ชนิดที่แยกได้จากเหง้ากระชายดำ (KD) เมื่อทดสอบฤทธิ์ยับยั้ง เอนไซม์อะเซทิลโคลีนเอสเตอเรส ด้วยวิธี microplate assay พบว่า สาร 6 (5,7,4’-trimethoxy-flavone) และ 7 (5,7-dimethoxyflavone) มีฤทธิ์ยับยั้งเท่ากับ 56.20 และ 44.20% ตามลำดับ ที่ระดับความเข้มข้น 1 มก. ต่อ มล. นอกจากนี้ยังได้สังเคราะห์สารฟลาโวน (11), 2’3’4’-trimethoxyflavone (12), 3,3’-dimethoxyflavone (13) และ 3-benzyloxy-3’methoxyflavone (14) พบว่าสาร 11, 13 และ 14 มีฤทธิ์ยับยั้งเอนไซม์อะเซทิลโคลีนเอสเตอเรสน้อยกว่าสาร 6 และ 7 ในการวิเคราะห์หาปริมาณสารฟลาโวนอยด์ (6 และ 7) ในสิ่งสกัดและผลิตภัณฑ์กระชายดำ ได้นำวิธีทาง HPLC แล

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