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Relevant bibliographies by topics / Benzyl

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Academic literature on the topic 'Benzyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 27 July 2025

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Journal articles on the topic "Benzyl"

1

Ledvina, Miroslav, Jiří Farkaš, Jaroslav Zajíček, Jan Ježek та Milan Zaoral. "An alternative synthesis of O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-(1→4)-N-acetylnormuramoyl-L-α-aminobutanoyl-D-isoglutamine". Collection of Czechoslovak Chemical Communications 54, № 10 (1989): 2784–94. http://dx.doi.org/10.1135/cccc19892784.

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Silver triflate-promoted condensation of 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl bromide (VIII) with benzyl 2-acetamido-6-O-benzoyl-2-deoxy-3-O-(methoxycarbonyl)-methyl-α-D-glucopyranoside (IV) afforded benzyl 2-acetamido-4-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-6-O-benzoyl-2-deoxy-3-O-(methoxycarbonyl)methyl-α-D-glucopyranoside (IX) which, after deprotection, was converted into the acid XI. Condensation of acid XI with L-α-aminobutanoyl-D-isoglutamine benzyl ester and subsequent hydrogenolysis of the product XIII furnished compound XIV. Benzyl 2-ac

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Krečmerová, Marcela, Hubert Hřebabecký, and Antonín Holý. "Preparation of 5-Benzyluracil and 5-Benzylcytosine Nucleosides as Potential Inhibitors of Uridine Phosphorylase." Collection of Czechoslovak Chemical Communications 61, no. 4 (1996): 627–44. http://dx.doi.org/10.1135/cccc19960627.

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Reaction of 3,4,6-tri-O-acetyl-2-deoxyglucopyranosyl bromide (1) with silylated 5-benzyluracil and subsequent ammonolysis afforded α- and β-anomers of 5-benzyl-1-(2-deoxy-D-glucopyranosyl)uracil (2 and 3). Under catalysis with tin tetrachloride, silylated 5-benzyluracil reacted with 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose to give 2',3',5'-tri-O-benzoyl-5-benzyluridine (10), which was converted into the 4-thio derivative 11 by reaction with Lawesson reagent. Debenzoylation of compound 11 afforded 5-benzyl-4-thiouridine (12), whereas its reaction with methyl iodide and deblocking gave 4-me

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Gainsford, Graeme J., Ralf Schwörer, Peter C. Tyler, and Olga V. Zubkova. "Crystal packing in three related disaccharides: precursors to heparan sulfate oligosaccharides." Acta Crystallographica Section E Crystallographic Communications 71, no. 6 (2015): 582–87. http://dx.doi.org/10.1107/s2056989015008518.

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The three title compounds form part of a set of important precursor dissacharides which lead to novel therapeutics, in particular for Alzheimer's disease. All three crystallize as poorly diffracting crystals with one independent molecule in the asymmetric unit. Two of them are isostructural: 4-methoxyphenyl 4-O-[6-O-acetyl-2-azido-3-O-benzyl-2-deoxy-4-O-(9-fluorenylmethyloxycarbonyl)-α-D-glucopyranosyl]-2-O-benzoyl-3-O-benzyl-6-O-chloroacetyl-α-L-idopyranoside, C59H56ClN3O16, (I), theido-relative of a reportedgluco-disaccharide [Gainsfordet al., 2013).Acta Cryst.C69, 679–682] and 4-methoxyphen

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Poonam, T. Agrawal, and P. Deshmukh Shirish. "Synthesis of new N-lactosylated isodithiobiurets and dithiazolidines (hydrobromide)." Journal of Indian Chemical Society Vol. 86, Jun 2009 (2009): 645–48. https://doi.org/10.5281/zenodo.5811842.

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P. G Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India <em>E-mail</em> : poonam.agrawal2008 @rediffmail.com <em>Manuscript received 23 May 2008, revised 10 February 2009, accepted 11 February 2009</em> A series of new 1-hepta-<em>O</em>-benzoyl-β-D-lactosyl-5-aryl-2-<em>S-</em>benzyl-2,4-isodithiobiurets and 3-hepta-<em>O</em>-benzoyl-β-D-Iactosylimino-5-arylimino-1,2,4-dithiazolidines (hydrobromide) have been synthesized by the interaction of hepta-<em>O</em>-benzoyl-β-D-lactosyl isothiocyanate with 1-aryl-<em>S</em>-benzyl isothiocarbamides follo

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Desai, T., J. Gigg та R. Gigg. "The Allyl Group for Protection in Carbohydrate Chemistry. XXXI. Conversion of Allyl 2,6-Di-O-benzyl-α-D-galactopyranoside Into Allyl 2,6-Di-O-benzyl-α-D-glucopyranoside and 2,6-Di-O-benzyl-D-glucopyranose". Australian Journal of Chemistry 49, № 3 (1996): 305. http://dx.doi.org/10.1071/ch9960305.

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Allyl 2,6-di-O-benzyl-α-D-galactopyranoside was converted by tin-mediated alkylation into the 3-O-p-methoxybenzyl ether which gave the 4-O-mesyl derivative. Sodium benzoate in refluxing N,N-dimethylformamide converted the last compound into allyl 4-O-benzoyl-2,6-di-O-benzyl-3-O-p-methoxybenzyl-α-D-glucopyranoside in high yield. This was saponified and the product was treated with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone to give the required allyl 2,6-di-O-benzyl-α-D-glucopyranoside whose structure was confirmed by conversion into the known 2,3,4,6-tetra-O-benzyl-D-glucopyranose. Removal of th

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Walji, Dhiran V. B., John M. D. Storey, and William T. A. Harrison. "BenzylN-benzyl-N-(2-formylphenyl)carbamate–benzylN-benzyl-N-(2-carboxyphenyl)carbamate [0.332 (4)/0.668 (4)]." Acta Crystallographica Section E Structure Reports Online 63, no. 4 (2007): o1575—o1576. http://dx.doi.org/10.1107/s1600536807009063.

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Wootton, Hannah S., та Gavin J. Miller. "Methyl and Benzyl (Ethyl 3,4-di-O-benzyl-2-O-benzoyl-1-thio-β-d-glucopyranosyl)uronate". Molbank 2024, № 3 (2024): M1847. http://dx.doi.org/10.3390/m1847.

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Methyl and benzyl (ethyl 3,4-di-O-benzyl-2-O-benzoyl-1-thio-β-D-glucopyranosyl)uronate were synthesised from a protected thioglycoside in three steps. A regioselective ring opening of the benzylidene acetal with BH3.THF generated C6-OH material, which was subsequently oxidised using biphasic TEMPO/BAIB conditions. The resultant uronic acid was esterified with either a methyl or benzyl moiety. The products were obtained on a multigram scale and fully characterised by 1H, 13C and 2D NMR, alongside MS and IR analysis.

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Stick, Robert V., Keith A. Stubbs, and Andrew G. Watts. "Modifying the Regioselectivity of Glycosynthase Reactions Through Changes in the Acceptor." Australian Journal of Chemistry 57, no. 8 (2004): 779. http://dx.doi.org/10.1071/ch04025.

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Successful glycosynthase-mediated reactions have been performed on 6-O-benzyl-, 6-O-(4-nitrobenzyl)-, and 6-O-benzoyl-d-glucopyranose to give 1,2-β- and 1,3-β-d-glycosylated products; 4-O-benzyl-d-xylopyranose gave only a 1,2-β-glycosylated product. A rationale is presented for these rather unusual results.

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Grehn, Leif, and Ulf Ragnarsson. "Synthesis and use of benzyl tert-butyl iminodicarbonate, a versatile reagent for the preparation of amines." Collection of Czechoslovak Chemical Communications 53, no. 11 (1988): 2778–86. http://dx.doi.org/10.1135/cccc19882778.

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An efficient synthesis of benzyl tert-butyl iminodicarbonate (IV), starting from benzoyl isocyanate, is reported. Reaction of the isocyanate with benzyl alcohol gave benzyl N-benzoylcarbamate (II) which on exhaustive tert-butoxycarbonylation via the non-isolated triacyl amine III, after aminolysis, provided the title compound. The sodium salt V was alkylated with various halides under Gabriel conditions to give in high yields the corresponding benzyloxycarbonyl tert-butoxycarbonyl diprotected amines. Similarly, compound IV was alkylated with alcohols under Mitsunobu conditions to give some add

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P., T. Agrawal, та P. Deshmukh S. "Synthesis and antimicrobial activity of 1-hepta-0-benzoyl-β-D-Iactosyl-5-aryl-2- S-benzyl-2,4-isodithiobiurets". Journal Of India Chemical Society Vol. 87, Nov 2010 (2010): 1395–98. https://doi.org/10.5281/zenodo.5805921.

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P.G. Department of Chemistry, Shri Shivaji College, Akola-444 001, Maharashtra, India Manuscript received 1 January 2009, revised 26 March 2010, accepted 7 April 2010 Several 1-hepta-<em>O</em>-benzoyl-β-D-lactosyl-5-aryl-2-S-benzyl-2,4-isodithiobiurets have been prepared by the interaction of I-hepta-<em>O</em>-benzoyl-β-D-lactosyl-2·S-benzyl isothioearbamide with aryl isothiocyanates. The structure of these new <em>N</em>-lactosylated-2,4-isodlthlobiurets have been established on the basis or usual chemical transformations and IR, NMR, and Mass spectral analysis. Antimicrobi

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Dissertations / Theses on the topic "Benzyl"

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Papageorgiou, Edward Andrew. "Selective hydrogenolysis of benzyl protective groups : novel methodology in the benzyl carbamate and benzyl amine series." Thesis, University of Cambridge, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.620936.

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Lin, Tai-Yuan David. "Laser-induced fluorescence spectroscopy of benzyl, methyl benzyl, and arylmethyl radicals /." The Ohio State University, 1991. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487694702784492.

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Gillooly, David John. "Benzyl alcohol dehydrogenase from Acinetobacter calcoaceticus." Thesis, University of Glasgow, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.309385.

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Fruteau, de Laclos Anne-Marie F. (Anne-Marie François). "Cleavage of benzyl aryl ethers by chlorine." Thesis, McGill University, 1991. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=70291.

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In order to extend application of the gel-degradation mechanism of delignification, model compounds of the general structure (3,4-dimethoxyphenyl)-CH(OR)R$ sp prime$ were treated at room temperature with increasing charges of molecular Cl$ sb2$ in glacial HOAc.<br>Catalytic amounts of Cl$ sb2$ cleaved benzyl aryl ether bonds (OR=2-methoxy-4-methylphenoxy) before any ring chlorination occurred. Yields of cleavage decreased in the order: R$ sp prime$=H; R$ sp prime$=$-$CH$ sb2$-2-methoxyphenoxy; R$ sp prime$=$-$CH(CH$ sb2$OH)-2-methoxyphenoxy. These results support the concept that the delignifi

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Arya, Nlin. "Modulation of carcinogen metabolism by benzyl isothiocyanate." Thesis, University of Surrey, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.494202.

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Precision-cut rat liver slices were incubated with various concentrations of benzyl isothiocyanate (BITC) (0-25 μM) for 24 hours. BITC decreased the dealkylation of ethoxy-(EROD) and methoxyresomfin (MROD) but increased CYP1A1/2 apoprotein levels; in vitro studies confirmed that it is mechanism-based inhibitor. BITC decreased both dealkylation of pentoxyresorufin (PROD) and CYP2B1 apoprotein levels but there was no effect on 7-benzyloxyquinoline (7-BQ) metabolism and CYP3A apoprotein levels. In the case of Phase II enzyme systems, BITC increased epoxide hydrolase and GST activity and a similar

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Ross, Jennifer Nicola. "Alkoxy- substituted aryl- and benzyl- organotin compounds." Thesis, University of Aberdeen, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324880.

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New organotin compounds containing alkoxy- functionalities have been prepared. The methods of preparation of the tetraorganotin species have involved three routes. Hydrostannation reactions using triphenyltin hydride have resulted in the synthesis of triphenyltin derivatives of a series of alkoxy- substituted allyl ethers. The addition of tin IV chloride, diphenyltin dichloride and phenyltin trichloride to alkoxy- substituted aryl- and benzyl- Grignard reagents have also been successful. Alkoxy- substituted benzyltin compounds have been prepared by following an alternative preparation of benzy

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Turnbull, Paul James Hardold. "The interaction of benzyl alcohol with lipid bilayers." Thesis, University of Leeds, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.252948.

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Mackintosh, Robert William. "Benzyl alcohol dehydrogenase and benzaldehyde dehydrogenase of Acinetobacter calcoaceticus." Thesis, University of Glasgow, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.281219.

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Jacobs, Jaco. "Poly(N-vinylpyrrolidone) - Poly(γ-benzyl-L-glutamate) conjugates". Stellenbosch : Stellenbosch University, 2012. http://hdl.handle.net/10019.1/20369.

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Thesis (MSc)--Stellenbosch University, 2012.<br>ENGLISH ABSTRACT: The combination of natural and synthetic polymers allow for the synthesis of advanced hybrid copolymers. These hybrid copolymers have applications in biomedical areas, one such area being in drug delivery systems (DDS). In this study, a modular approach was used to prepare amphiphilic block copolymers with the ability to self-assemble into three dimensional structures. Reversible addition-fragmentation chain transfer (RAFT) was the synthetic tool used to mediate the polymerization of N-vinylpyrrolidone. RAFT is a versatile

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Rahaingoson, Farasoa. "Synthèse et étude comparative de l'activité antifongique de benzyl 2-furylcétones alpha-bromées et de benzyl 2-furylcétones alpha-fluorées : corrélation structure-activité." Toulouse, INPT, 1993. http://www.theses.fr/1993INPT052G.

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Dans le cadre de la recherche de nouveaux produits antifongiques, nous nous sommes proposes de synthetiser la serie de benzyl 2-furylcetones -bromees et la serie de benzyl 2-furylcetones -fluorees diversement substitues. La bromation et la fluoration de la serie de benzyl 2-furylcetones se font en deux etapes. La premiere etape est une bromation de benzyl 2-furylcetones par la resine anionique a#1#6#2br#3#. La deuxieme etape est une fluoration nucleophile de benzyl 2-furylcetones -bromees par la resine anionique a#2#6f#. Les rendements eleves obtenus a chaque etape soulignent l'efficacite et l

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Books on the topic "Benzyl"

1

Ms, Meek M. E., World Health Organization, International Program on Chemical Safety., and Inter-Organization Programme for the Sound Management of Chemicals., eds. Butyl benzyl phthalate. World Health Organization, 1999.

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Programme, United Nations Environment, International Labour Organisation, World Health Organization, Inter-Organization Programme for the Sound Management of Chemicals, and International Program on Chemical Safety, eds. Butyl benzyl phthalate. World Health Organization, 1999.

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. Benjiru kurorido (betsumei enka benjiru): Benzyl chloride. Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2009.

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Kagaku Busshitsu Hyōka Kenkyū Kikō and Shin Enerugī Sangyō Gijutsu Sōgō Kaihatsu Kikō (Japan), eds. Futaru-san-n-buchiru benjiru: N-butyl benzyl phthalate. Seihin Hyōka Gijutsu Kiban Kikō Kagaku Busshitsu Hyōka Kenkyū Kikō, 2007.

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5

Koerner, Terry. Using kinetic isotope effects to model the transition states for the sn2 reactions between sodium borohydride and para-substituted benzyl chlorides. Laurentian University Press, 1996.

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Bruce, Cook. The Feasibility of measuring the rate constant and secondary [alpha]-deuterium kinetic isotope effect for the Sn2 reaction between sodium phenoxide and benzyl chloride at low concentrations of phenoxide ion. Laurentian University, 1995.

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7

Smith, Wilbur A. Bencil. Altin Kitaplar Yayinevi, 1997.

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Cabanillas, José Julio. Benzelá. Pre-Textos, 1998.

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International Centre for Bengal Studies., ed. Bengal partition 1905 and East Bengal. International Centre for Bengal Studies, 2008.

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Éliade, Mircea. Bengal nights. University of Chicago Press, 1994.

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Book chapters on the topic "Benzyl"

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Gooch, Jan W. "Benzyl." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1230.

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Bährle-Rapp, Marina. "Benzyl Acetate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1093.

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Bährle-Rapp, Marina. "Benzyl Alcohol." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1094.

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Bährle-Rapp, Marina. "Benzyl Benzoate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1095.

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Bährle-Rapp, Marina. "Benzyl Cinnamate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1096.

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Bährle-Rapp, Marina. "Benzyl Hyaluronate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1099.

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Bährle-Rapp, Marina. "Benzyl Laurate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1103.

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Bährle-Rapp, Marina. "Benzyl Nicotinate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1104.

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Bährle-Rapp, Marina. "Benzyl Salicylate." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_1106.

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Gooch, Jan W. "Benzyl Abietate." In Encyclopedic Dictionary of Polymers. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1231.

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Conference papers on the topic "Benzyl"

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Kopecky, Sarah E. "Investigation of Substituent Effects on the Corrosion Inhibition of Pyridine Derivatives with Acetylenic Alcohols on Steel in Acid Media." In CORROSION 2015. NACE International, 2015. https://doi.org/10.5006/c2015-05569.

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Abstract The corrosion inhibition of substituted pyridine derivatives and quaternized pyridines in the presence and absence of acetylenic alcohol synergists is reported. Electrochemical Frequency Modulation (EFM) was used as a method of monitoring corrosion rates of steel in acidic environments. Early stage pitting was evaluated via scanning electron microscope (SEM) for comparison of measured corrosion rates to observed pit formation. EFM was found to be a reliable and accurate method of monitoring general corrosion rates over time, and causality factor data was found to depend heavily on the

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wang, chengxia. "Binary Co3@CdS composite for photocatalytic oxidation of benzyl alcohol coupling with hydrogen generation." In Tenth International Conference on Energy Materials and Electrical Engineering (ICEMEE 2024), edited by Yuanhao Wang and Cristian Paul Chioncel. SPIE, 2024. https://doi.org/10.1117/12.3050510.

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Gulbrandsen, Egil, Rolf Nyborg, Trine Løland, and Kemal Nisancioglu. "Effect of Steel Microstructure and Composition on Inhibition of CO2 Corrosion." In CORROSION 2000. NACE International, 2000. https://doi.org/10.5006/c2000-00023.

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Abstract The effects of steel microstructure and composition on the inhibition of CO2 corrosion were studied at 25 °C, pH 5, 1 bar CO2 in 3 % NaCl solutions. Generic inhibitor compounds cocoalkyl-dimethyl-benzyl ammonium chloride (QUAT) and sodium thiosulfate (THIO) were used. Sixteen different carbon steels were tested with a blend of 40 ppm QUAT and 0.5 ppm THIO. The test specimens were precorroded for six days in the corrosive medium prior to inhibitor addition. The effect of inhibitors was assessed by electrochemical polarization tests. The inhibitor efficiency ranged from 84 to 98 %. The

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Eiden, G. C., and J. C. Weisshaar. "Threshold photoelectron spectroscopy of benzyl radical with cm−1 resolution." In OSA Annual Meeting. Optica Publishing Group, 1992. http://dx.doi.org/10.1364/oam.1992.thi2.

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Pulsed field ionization (PFI)1 is used to record vibrational bands from 0 to 2100 cm−1 for ben-zyl+–-h7′, benzyl+–αd2, and benzy+–d7. Over 100 vibrational states are observed; assignments utilizing ab initio calculations identify 12 normal modes. Our data for benzyl+firmly establishes the accuracy of the calculations, which are typically 2–3% higher than experiment. Comparison of the ab initio frequencies for benzyl radical and cation show substantially greater double bond character in the exocyclic C-C bond in the cation than in that of the radical. PFI spectra recorded via each of the neutra

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Olivares-Pérez, A., S. Toxqui-López, I. Fuentes-Tapia, and V. Dorantes-Garcia. "Holograms with fluorescent benzyl." In SPIE OPTO, edited by Hans I. Bjelkhagen. SPIE, 2011. http://dx.doi.org/10.1117/12.875144.

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Han, Kai, Geng Fu, Changlu Zhao, Bolan Liu, and Shibo Ma. "An Experimental Study of the Vaporization Characteristics of Diesel-Benzyl Azides Blend Droplets." In ASME 2013 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icef2013-19072.

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An experimental study of diesel-benzyl azides blend droplets vaporization characteristics was carried out to study the reasons of diesel-benzyl azides blend shortened combustion duration using suspended droplet device and a high-speed video camera. Experiments were performed at atmospheric pressure, ambient temperature range 480–933 K, and initial droplet diameter of 0.98, 1.42, 1.88 mm. The results show a shorten in diesel-benzyl azides blend droplet lifetime by 10% compared to diesel droplet at 1.42 mm initial droplet diameter and 933 K ambient temperature companion to puffing. The above res

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Guangwei Qiao, Lihua Jia, Xueju Zhang, and Xiangfeng Guo. "Liquid-phase catalytic oxidation of benzyl alcohol to benzyl aldehyde With Fe/La-HMS." In 2011 International Conference on Remote Sensing, Environment and Transportation Engineering (RSETE). IEEE, 2011. http://dx.doi.org/10.1109/rsete.2011.5965955.

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Wang, Jun, Hiroyuki Niino, and Akira Yabe. "Laser ablation of PMMA doped with benzyl." In Photonics China '98, edited by ShuShen Deng and S. C. Wang. SPIE, 1998. http://dx.doi.org/10.1117/12.317934.

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Weisshaar, James C. "Photoelectron spectroscopy with cm-1resolution: VO+, benzyl+, toluene+." In OE/LASE '92, edited by Cheuk-Yiu Ng. SPIE, 1992. http://dx.doi.org/10.1117/12.58157.

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Lopanov, A. N., V. V. Evdokimov, N. P. Zuev, V. A. Lusich, and S. N. Zuev. "Antibacterial Activity of Benzyl Penicillin Water Solutions With Silver." In The International Conference “Health and wellbeing in modern society” (ICHW 2020). Atlantis Press, 2020. http://dx.doi.org/10.2991/ahsr.k.201001.008.

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Reports on the topic "Benzyl"

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ชัยเจริญพงศ์, จรรยา. การสังเคราะห์อนุพันธ์ของคาร์เพสเตอรอลและฤทธิ์ยับยั้งไลเพส : รายงานการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2014. https://doi.org/10.58837/chula.res.2014.94.

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อนุพันธ์ของสารคาร์เพสเตอรอล (13-15) ถูกสังเคราะห์ขึ้นโดยเปลี่ยนหมู่ฟังก์ชันไฮดรอกซิที่ตำแหน่ง C22 ไปเป็นหมู่ acetyl (13) หมู่ benzyl (14) และหมู่ benzoyl (15) สารเหล่านี้แสดงฤทธิ์ยับยั้งไลเพสด้วยค่าเปอร์เซ็นต์การยับยั้งไลเพส เท่ากับ 72.60 ± 5.9%, 87.82 ± 3.00% และ 81.26 ± 3.64% ตามลำดับ ที่ความเข้มข้น 1.25 mg/ml ขณะที่สารคาร์เพสเตอรอลแสดงฤทธิ์ยับยั้งไลเพสด้วยค่าเปอร์เซ็นต์การยับยั้งไลเพส เท่ากับ 62.3 ± 6.2% ที่ความเข้มข้นเดียวกัน นอกจากนี้ยังทดสอบฤทธิ์ยับยั้งไลเพสของสารที่มีโครงสร้างหลักคล้ายคาร์เพสเตอรอล ได้แก่ stigmasterol, β-sitosterol, campesterol และ cholesterol พบว่าสารทั้งสี่มีฤทธิ์ยับย

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2

Mudge, Christopher, Bradley Sartain, Kurt Getsinger, and Michael Netherland. Efficacy of florpyrauxifen-benzyl on dioecious hydrilla and hybrid water milfoil - concentration and exposure time requirements. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/42062.

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This study conducted small-scale trials under various concentration and exposure time (CET) scenarios to determine florpyrauxifen-benzyl activity on dioecious hydrilla and hybrid watermilfoil and determine impact on water stargrass and elodea. Hydrilla treated with 12, 24, or 36 μg active ingredient (a.i.) L⁻¹ florpyrauxifen-benzyl and exposed for 12, 24, or 48 hr under outdoor mesocosm conditions was reduced in biomass by 30-75% at 8 weeks after treatment (WAT). An additional hydrilla trial at the same herbicide concentrations, but under longer exposures (24, 72, or 168 hr), resulted in 33–85

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3

Mudge, Christopher, Bradley Sartain, Benjamin Sperry, and Kurt Getsinger. Efficacy of florpyrauxifen-benzyl for eurasian watermilfoil control and nontarget Illinois pondweed, elodea, and coontail response. Engineer Research and Development Center (U.S.), 2021. http://dx.doi.org/10.21079/11681/42063.

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This research evaluated low concentrations and short exposure times of the recently registered aquatic herbicide florpyrauxifen-benzyl (4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoro-pyridine-2-benzyl ester) on the target plant Eurasian watermilfoil (Myriophyllum spicatum L., hereafter referred to as EWM) as well as selectivity towards the nontarget submersed species Illinois pondweed (Potamogeton illinoensis Morong), elodea (Elodea canadensis Michx.), and coontail (Ceratophyllum demersum L.)

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4

Bernstein, E. R., and H. S. Im. Mass Resolved Excitation Spectroscopy of Benzyl and Phenylnitrene Radicals. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada239394.

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Sartain, Bradley, Erika Haug, Kurt Getsinger, Benjamin Sperry, Mark Heilman, and Mike Greer. Small plot applications of florpyrauxifen–benzyl (Procellacor SC™) for control of monoecious hydrilla in Roanoke Rapids Lake, NC. Engineer Research and Development Center (U.S.), 2023. http://dx.doi.org/10.21079/11681/47115.

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Four demonstration plots were selected at Roanoke Rapids Lake, NC to evaluate water exchange and aqueous herbicide residues in stands of submersed aquatic vegetation (SAV) following treatment with rhodamine wt dye and florpyrauxifen-benzyl to control monecious hydrilla. Florpyrauxifen-benzyl (Procellacor™ SC) was applied in combination with Rhodamine WT (RWT) at two of the plots. Dye measurements and herbicide residue samples were collected at specific time intervals to draw comparisons between herbicide and RWT dye dissipation. The two additional plots served as reference plots to the treatme

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6

Li, S., and E. R. Bernstein. Benzyl Alcohol-Water and -Ammonia Clusters: Ion Fragmentation and Chemistry. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada255745.

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7

Schneider, D. A., D. A. Loy, B. M. Baugher, et al. Preparation and characterization of phenyl-, benzyl-, and phenethyl-substituted polysilsesquioxanes. Office of Scientific and Technical Information (OSTI), 1998. http://dx.doi.org/10.2172/658253.

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8

ตันฑุลานิ, ธวัชชัย, та วิทยา เรืองพรวิสุทธิ์. การสังเคราะห์เอซาคราวน์อีเธอร์คาลิก[4]ซารีนชนิดใหม่และการศึกษาการจับกับแคทไอออน แอนไอออน และอินทรีย์โมเลกุล : รายงานวิจัยฉบับสมบูรณ์. จุฬาลงกรณ์มหาวิทยาลัย, 2001. https://doi.org/10.58837/chula.res.2001.48.

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วัตถุประสงค์ : เพื่อพัฒนาวิธีการสังเคราะห์เอซาคาลิกซารีนที่มีหมู่เอมีนแบบต่างๆ และศึกษาสมบัติในการจับกับแคทไออน แอนไอออน และโมเลกุลอินทรีย์ของสารที่สังเคราะห์ได้ ตลอดจนศึกษาความเป็นไปได้ในการนำสารที่สังเคราะห์ได้มาประยุกต์ใช้งานในการแยกโลหะไออน และอินทรีย์โมเลกุลออกจากสิ่งแวดล้อม ระเบียบวิธีวิจัย : ปฏิกิริยาคอนแดนเซชันระหว่างอนุพันธ์อัลดีไฮด์ของคาลิก [4] ซารีนและเอมีนที่เหมาะสมจะให้ผลิตภัณฑ์เป็นสารรูปชิฟเบส จากนั้นทำการรีดิวซ์สารชิฟเบสด้วย NaBH[subscript 4] แล้วโปรตอนเนท ด้วย HCI ใน CH[subscript3]OH จะได้ผลิตภัณฑ์รูปแอมโมเนียมออกมา จากนั้นทำปฏิกิริยาสะเทินกับ NaOH จะได้สารประกอบเอซาเบนซินคราวน

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9

Mudge, Christopher, and Michael Netherland. Evaluation of new endothall and florpyrauxifen-benzyl use patterns for controlling crested floating heart and giant salvinia. Engineer Research and Development Center (U.S.), 2020. http://dx.doi.org/10.21079/11681/38859.

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The purpose of this research was to (1) evaluate concentration exposure time (CET) relationships for florpyrauxifen-benzyl (ProcellaCOR) for control of the floating leaved plant crested floating heart (Nymphoides cristata, CFH) and (2) evaluate foliar applications of endothall (Aquathol K) for control of CFH and the floating fern giant salvinia (Salvinia molesta).

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10

Im, Hoong-Sun, and E. R. Bernstein. Determination of the Minimum Energy Conformations of Benzyl Alcohol and 2-Phenethyl Alcohol. Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada216972.

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