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Dissertations / Theses on the topic 'Benzyloxy'

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

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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9

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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10

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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11

CHEN, KUAN-FU, and 陳冠甫. "The study of the benzoyl-migration behavior in 1-benzyloxy-3-(p-nitrobenzoyl)oxycalix[4]arene." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/51419720245680451212.

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碩士<br>中國文化大學<br>化學系應用化學碩士班<br>103<br>Calixarenes, which are cyclic oligomers of p-substituted phenols and formaldehyde, are able to include small organic molecules or metal ions within molecular cavities to form the “host-guest complexes”. In the literature, four different kinds of calix[4]arene ether derivatives (monoalkoxy-, 1,3-dialkoxy-, trialkoxy-, and tetra- alkoxycalix[4]arenes) had been reported. To achieve the preparation of last set of calix[4]arene ether derivative (1,2-dialkoxycalix[4]arenes), a multi-step synthesis route was developed by this laboratory. An unexpecting benzoyl-
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12

Pein, Miriam Katharina [Verfasser]. "Synthese und antiparasitäre Eigenschaften von N-(Benzyloxy)-N-́(3-hydroxypyridin-2-yl)harnstoffen / vorgelegt von Miriam Pein." 2008. http://d-nb.info/992426014/34.

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13

許清雲. "Approaches to the Total Synthesis of (+)-Herbicidin B Enantioselective Syntheses of (2S)-1-Benzyloxy-2,3-propanediol and (2R)-1-Amino-2,3-propanediol from Glycerol." Thesis, 1991. http://ndltd.ncl.edu.tw/handle/f6ecst.

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14

Chen, Pin-Zu, та 陳品如. "Part1. Chiral Syn-Aldol Reaction Studies of Chiral γ- Benzyloxy Subsituted Vinylogous Urethanepart2. Chiral [2,3]-Wittig rearrangement Studies of Chiralγ- Allyloxy Subsituted Vinylogous Urethane". Thesis, 2004. http://ndltd.ncl.edu.tw/handle/chmeck.

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碩士<br>朝陽科技大學<br>應用化學系碩士班<br>92<br>1.Chiral Syn-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 syn-aldol adduct, the selectivity of this product was analyzed using chiral column to determine their enantio- selectivity and diastereoselectivity. 2.Chiral [2,3]-Wittig rearrangement Reaction Studies of Chiral γ-Allyloxy Subsituted Vinylogous Urethane Dienolates of various chiral γ-allyloxy subsituted vinylogous urethane undergo a [2,3]-Wittig rearrangement
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15

賴玉琪. "Synthesis and biological activities of (2E)-3-[2-(substituted benzyloxy0-4(or 5) methoxyphenyl] acrylaldehyde derivatives." Thesis, 2003. http://ndltd.ncl.edu.tw/handle/01580863496631727352.

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16

Bieg, Tadeusz. "Synteza selektywnie zabezpieczonych cukrów w reakcji hydrogenolizy eterów benzylowych i acetali pochodnych aldehydu benzoesowego." Rozprawa doktorska, 1986. https://repolis.bg.polsl.pl/dlibra/docmetadata?showContent=true&id=3599.

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17

Bieg, Tadeusz. "Synteza selektywnie zabezpieczonych cukrów w reakcji hydrogenolizy eterów benzylowych i acetali pochodnych aldehydu benzoesowego." Rozprawa doktorska, 1986. https://delibra.bg.polsl.pl/dlibra/docmetadata?showContent=true&id=3599.

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