Thematische Bibliographien / Aryl Y

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Auswahl der wissenschaftlichen Literatur zum Thema „Aryl Y“

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Veröffentlicht am 18. Mai 2024

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Zeitschriftenartikel zum Thema "Aryl Y"

Wang, Xi-Cun, Fang Wang, Zheng-Jun Quan, Man-Gang Wang und Zheng Li. „An efficient and clean synthesis of 1-aroyl-3-aryl-4-substituted imidazole-2-thiones in water“. Journal of Chemical Research 2005, Nr. 11 (November 2005): 689–90. http://dx.doi.org/10.3184/030823405774909423.

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Treatment 1-aryl-3-aroyl/benzofuroyl thioureas with α-bromo substituted carbonyl compounds in water affording 1-aroyl/benzofuroyl-3-aryl-4-substituted imidazole-2-thiones in excellent yields within short time.

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Steparuk, Elena V., Dmitrii L. Obydennov und Vyacheslav Y. Sosnovskikh. „Synthesis of 5-Aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones“. Molbank 2023, Nr. 2 (10.06.2023): M1668. http://dx.doi.org/10.3390/m1668.

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A two-stage synthesis of 5-aroyl-2-aryl-3-hydroxypyridin-4(1H)-ones (56–66% overall yields) was carried out by refluxing 5-aroyl-3-(benzyloxy)-2-(het)aryl-4H-pyran-4-ones with ammonium acetate in AcOH and subsequent debenzylation. The prepared N-unsubstituted 4-pyridones exist in the pyridone tautomeric form.

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Ying, Jun, Zhengjie Le, Zhi-Peng Bao und Xiao-Feng Wu. „Palladium-catalyzed double carbonylation of propargyl amines and aryl halides to access 1-aroyl-3-aryl-1,5-dihydro-2H-pyrrol-2-ones“. Organic Chemistry Frontiers 7, Nr. 8 (2020): 1006–10. http://dx.doi.org/10.1039/d0qo00007h.

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Passananti, Monica, Flavio Cermola, Marina DellaGreca, Maria Rosaria Iesce, Lucio Previtera, Rosalia Sferruzza und Fabio Temussi. „Photochemical Behaviour of Carbamates Structurally Related to Herbicides in Aqueous Media: Nucleophilic Solvent Trapping versus Radical Reactions“. International Journal of Photoenergy 2014 (2014): 1–6. http://dx.doi.org/10.1155/2014/864361.

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Irradiation ofN-arylO-aryl carbamates has been carried out in H2O/CH3CN (1 : 1 v/v) solutions atλ>290 nm. When chlorine is on theN-aryl ring, halogen-substituted products are found. These photoproducts derive from the trapping of the intermediate radical cation by water and, even, by acetonitrile leading to phenols andN-arylacetamides (photo-Ritter products), respectively. UnsubstitutedN-aryl carbamates slowly undergo photo-Fries reaction.

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Jugelt, W. „Über Aryl-aroyl-diazomethane“. Zeitschrift für Chemie 5, Nr. 12 (02.09.2010): 455–56. http://dx.doi.org/10.1002/zfch.19650051206.

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Mkrtchyan, Satenik, Michał Jakubczyk, Suneel Lanka, Michael Pittelkow und Viktor O. Iaroshenko. „Cu-Catalyzed Arylation of Bromo-Difluoro-Acetamides by Aryl Boronic Acids, Aryl Trialkoxysilanes and Dimethyl-Aryl-Sulfonium Salts: New Entries to Aromatic Amides“. Molecules 26, Nr. 10 (16.05.2021): 2957. http://dx.doi.org/10.3390/molecules26102957.

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We describe a mechanism-guided discovery of a synthetic methodology that enables the preparation of aromatic amides from 2-bromo-2,2-difluoroacetamides utilizing a copper-catalyzed direct arylation. Readily available and structurally simple aryl precursors such as aryl boronic acids, aryl trialkoxysilanes and dimethyl-aryl-sulfonium salts were used as the source for the aryl substituents. The scope of the reactions was tested, and the reactions were insensitive to the electronic nature of the aryl groups, as both electron-rich and electron-deficient aryls were successfully introduced. A wide range of 2-bromo-2,2-difluoroacetamides as either aliphatic or aromatic secondary or tertiary amides were also reactive under the developed conditions. The described synthetic protocols displayed excellent efficiency and were successfully utilized for the expeditious preparation of diverse aromatic amides in good-to-excellent yields. The reactions were scaled up to gram quantities.

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Bhaskar Reddy, Dandu, Biradavolu Seenaiah, Adivireddi Padmaja und Pallela Venkata Ramana Reddy. „Synthesis of Some New Bis[1-(2-aroyl-3-aryl)cyclopropylcarbonyl]benzenes and Pyridines under Phase Transfer Catalysis (PTC) Method“. Collection of Czechoslovak Chemical Communications 58, Nr. 6 (1993): 1437–44. http://dx.doi.org/10.1135/cccc19931437.

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Some new bis[1-(2-aroyl-3-aryl)cyclopropylcarbonyl]benzenes and pyridines IV - VI have been prepared by the cycloaddition of dimethylsulfonium phenacylide to 1,1'-(1,3-, 1,4-phenylene, and 2,6-pyridylene)-bis(3-aryl-2-propen-1-ones) I - III by adopting two different methods. The advantages of the PTC method over the other have been discussed. The structures of the compound have been confirmed by spectral data.

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Rasheed, O. K., I. R. Hardcastle, J. Raftery und P. Quayle. „Aryne generation vs. Truce-Smiles and fries rearrangements during the Kobayashi fragmentation reaction: a new bi-aryl synthesis“. Organic & Biomolecular Chemistry 13, Nr. 29 (2015): 8048–52. http://dx.doi.org/10.1039/c5ob01239b.

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Glaum, Marcus, Wolfgang Kläaui, Brian W. Skelton und Allan H. White. „Synthesis, X-Ray Crystal Structure and Reactivity of [(tmeda)(p-tolyl)Pd(μ2-I)AgL], an Unusual Silver Iodide Complex; Reversible CO Insertion into the Pd-C Bond of [Pd(PPh3)(p-tolyl)L] (L - = [(C5H5)Co{P(OR)2O}3] - , R = Me, Pri)“. Australian Journal of Chemistry 50, Nr. 11 (1997): 1047. http://dx.doi.org/10.1071/c97074.

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The palladium complexes [Pd(PPh3)(aryl)LOR] (aryl = Ph, p-tolyl; LOR¯ = [(C5H5)Co{P(OR)2O}3]¯, R = Me, Pri) have been prepared by reaction of [PdI(aryl)(tmeda)] (tmeda = N,N,N′,N′-tetramethyl-ethylenediamine) with the silver salts AgLOR in the presence of PPh3. The complexes [Pd(PPh3)(aryl)LOR] rapidly and reversibly insert carbon monoxide to yield the aroyl palladium complexes [Pd(PPh3)(C(O)- p-tolyl)LOR] (R = Me, Pri ). The palladium iodide complex [PdI(p-tolyl)(tmeda)] and the silver salt AgLOR in the absence of PPh3 form an unusual adduct [(p-tolyl)(tmeda)Pd(µ2-I)AgLOMe] that contains a short silver-iodide bond (Ag-I 2 · 703(1) Å). The silver-palladium bond is bridged by iodine (Pd-Ag 3 · 011(1), Pd{I 2 · 5934(9) Å) and the silver atom is coordinated by the tris-chelating oxygen ligand LOMe.

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Quesnel, Jeffrey S., Alexander Fabrikant und Bruce A. Arndtsen. „A flexible approach to Pd-catalyzed carbonylations via aroyl dimethylaminopyridinium salts“. Chemical Science 7, Nr. 1 (2016): 295–300. http://dx.doi.org/10.1039/c5sc02949j.

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Dissertationen zum Thema "Aryl Y"

MORIN, ISABELLE. „3-aryl as-triazines : bioisosterie avec les 6-aryl pyridazines“. Université Louis Pasteur (Strasbourg) (1971-2008), 1991. http://www.theses.fr/1991STR13021.

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Un examen comparatif de bioisosteres potentiels de derives pyridaziniques (pyrazines, pyrimidines, 1,3,4-thiadiazoles, et 1,2,4-triazines) a ete realise. Les structures etablies par diffraction aux rayons x suivies de calculs semi-empiriques ont mis en evidence l'importance du moment dipolaire comme critere de differenciation entre ces differents systemes heterocycliques. Le systeme as-triazinique, predit comme devant etre bioequivalent des pyridazines a ete plus particulierement etudie. Sur le plan chimique, des ameliorations ont ete apportees a leur synthese au depart de derives d'hippurate d'ethyle. La reactivite du systeme a egalement ete etudiee, en particulier par la mise au point d'aminoalkyltriazines et de triazolotriazines. Une vingtaine d'aminoalkyltriazinones ont ete etudiees pour leurs proprietes analgesiques. Les affinites micromolaires de ces derives envers les recepteurs opiaces sigma et kappa concordent avec les valeurs moderees observees sur des tests d'analgesie chez l'animal. Des predictions d'activite inhibitrice de l'acetylcholinesterase pour des alkylaminotriazines se sont averees verifiees et demontrent a nouveau la bioequivalence entre les triazines et les pyridazines et l'absence de bioequivalence entre la pyrazine et les pyridazines. Au depart d'une dizaine de molecules synthetisees, plusieurs se sont revelees interessantes comme inhibiteur competitif et reversible de l'acetylcholinesterase; la plus puissante montrant une ic#5#0 de 3. 10#-#7 m

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Barman, Gopa. „Synthetic studies on N - Aryl Y - Lactam & N - Aryl Y - Thio - Lactam : chemoselective Transformation to N-Aryl-Pyrrolidine, N-Aryl Succinimide and Other Bioactive Compounds“. Thesis, University of North Bengal, 2009. http://hdl.handle.net/123456789/1379.

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Zhou, Edouard. „Nouveaux systèmes catalytiques appliqués aux formations de liaisons C—C par couplage croisé catalysé par des sels de fer : applications, mécanismes“. Thesis, Paris Sciences et Lettres (ComUE), 2018. http://www.theses.fr/2018PSLEC008.

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Gramberg, Joachim. „Synthese von threo-3-Aryl-glutaminsäurediethylestern und cis-3-Aryl-prolinen /“. [S.l. : s.n.], 1996. http://www.gbv.de/dms/bs/toc/225111152.pdf.

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Leyva-Ramos, Elisa. „The temperature dependent photochemistry of aryl azides and aryl diazo compounds /“. The Ohio State University, 1986. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487267024997622.

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Sun, Qingqing. „Aryl and Super Aryl-Extended Calix[4]pyrroles: Synthesis and Applications“. Doctoral thesis, Universitat Rovira i Virgili, 2021. http://hdl.handle.net/10803/672268.

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Aquesta tesi doctoral descriu el disseny i la síntesi d’una sèrie de receptors supramoleculars que presenten cavitats aromàtiques polars. Els receptors preparats inclouen receptors organometàl·lics, contenidors moleculars solubles en aigua, caixes moleculars basades en enllaços de coordinació i metal·lo-cavitands. S’han seleccionat unitats de calix[4]pirrole aril i super-aril estesos (AEC[4]P i SAE-C[4]P) com a components principals. S’han estudiat les propietats de reconeixement molecular dels receptors sintètics amb sals de clorur de tetraalquilamoni, així com de molècules polars neutres, en dissolvents orgànics i en aigua. Concretament, s’ha preparat un calix[4]pirrole super aril estès substituït amb una fosfina mono-Au(I) i s’han estudiat les seves propietats de reconeixement davant diferents sals de clorur de tetraalquilamoni en diclorometà i acetona. Els complexos organometàl·lics d'inclusió amb aquestes sals presenten una estabilitat termodinàmica reduïda respecte al seu anàleg no organometàlic simètric "de dues parets". Molt probablement això és degut a que les interaccions repulsives anió-π són més fortes al complex de clorur del receptor organometàl·lic. S’ha explorat l'aplicació d'un receptor SAE-C[4]P soluble en aigua en la hidròlisi de bis-isonitrils alifàtics catalitzada per àcids. El receptor SAE-C[4]P forma complexos 1:1 termodinàmicament estables amb els bis-isonitrils, mono-isonitrils-mono-formamides i bis-formamides. Els compostos mono reaccionats units presenten el grup formamida exclusivament en la conformació cis. Aquesta disposició protegeix el grup isonitril i provoca millores en el rendiment dels compostos mono-reaccionats. També s’ha dut a terme l’auto assemblatge d’una caixa metàl·lica soluble en aigua amb dos llocs d’unió polar endoèdrics. S’ha demostrat que l’assemblatge eficient de la caixa metàl·lica requereix l’encapsulació de molècules polars mono i ditòpiques neutres. La caixa metàl·lica mostra selectivitat conformacional per la unió de bis-formamides alifàtiques amb diferents longituds del espaiadors (grups metilè). Finalment, es descriu la síntesi d'un lligand tetra-oxazolo [4,5-b]pirazinil SAE-C[4]P sense precedents. Es descriu l’auto assemblatge d’un bis-metal·lo-cavitand basat en el lligand SAE-C[4]P i Pt(II) com a precursors. De la mateixa manera, es demostra que la inc
Esta tesis doctoral describe el diseño y la síntesis de una serie de receptores supramoleculares que presentan cavidades aromáticas polares. Los receptores preparados incluyen receptores organometálicos, contenedores moleculares solubles en agua, cajas moleculares basadas en enlaces de coordinación y metalo-cavitandos. Se han seleccionado unidades de calix[4]pirrol aril- y super-aril extendidos (AEC[4]P y SAE-C[4]P) como componentes principales. Se han estudiado las propiedades de reconocimiento molecular de los receptores sintéticos con sales de cloruro de tetraalquilamoni, así como de moléculas polares neutras, en disolventes orgánicos y en agua. Concretamente, se ha preparado un calix[4]pirrol super-aril extendido sustituido con una fosfina mono-Au(I) y se han estudiado sus propiedades de reconocimiento molecular ante diferentes sales de cloruro de tetraalquilamonio en diclorometano y acetona. Los complejos organometálicos de inclusión con estas sales presentan una estabilidad termodinámica reducida respecto a su análogo no organometálico simétrico "de dos paredes". Muy probablemente esto se debe a que las interacciones repulsivas anión-π son más fuertes en el complejo de cloruro del receptor organometálico. Se ha explorado la aplicación de un receptor SAE-C[4]P soluble en agua en la hidrólisis de bis-isonitrilos alifáticos catalizada por ácidos. El receptor SAE-C[4]P forma complejos 1: 1 termodinámicamente estables con los bis-isonitrilos, mono-isonitrilos-mono-formamida y bis-formamida. Los compuestos mono-reaccionados unidos presentan el grupo formamida exclusivamente en la conformación cis. Esta disposición protege el grupo isonitrilo y produce mejoras en el rendimiento de los compuestos mono-reaccionados. También se ha llevado a cabo el auto ensamblaje de una caja metálica soluble en agua con dos sitios de unión polar endoèdricos. Se ha demostrado que el ensamblaje eficiente de la caja metálica requiere la encapsulación de moléculas polares mono y di-tópicas neutras. La caja metálica muestra selectividad conformacional para la unión de bis-formamida alifáticas con diferentes longitudes de espaciadores (número de grupos metileno). Finalmente, se describe la síntesis de un ligando tetra-oxazolo [4,5-b] pirazinil SAE-C[4]P sin precedentes. Se describe el auto ensamblaje de un bis-metalo-cavitando basado
This PhD Thesis describes the design and synthesis of a series of supramolecular receptors featuring polar aromatic clefts and cavities. The prepared receptors include organometallic receptors, water-soluble containers, metallocages and metallocavitands. We selected aryl and super aryl-extended calix[4]pyrrole scaffolds (AE-C[4]P and SAE-C[4]P) as their main building blocks. We studied the molecular recognition properties of the synthetic receptors with tetraalkylammonium chloride salts, as well as neutral polar guests, in organic solvents and in water. Specifically, we prepared a mono-gold(I) phosphine substituted AE-C[4]P and studied its binding properties towards tetraalkylammonium chloride salts in dichloromethane and acetone solutions. The inclusion organometallic complexes featured a reduced thermodynamic stability with respect to its parent symmetrical “two-wall” counterpart. These results were explained considering the stronger repulsive anion-π interactions present in the chloride complex of the organometallic receptor. Next, we explored the application of a water-soluble SAE-C[4]P in the acid-catalyzed hydrolysis of aliphatic bis-isonitriles. The SAE-C[4]P receptor formed thermodynamically stable 1:1 complexes with the bis-isonitriles, mono-isonitrile-mono-formamides and bis-formamides. The bound mono-reacted compounds featured the formamide group in exclusive cis-conformation. This arrangement protected the unreacted isonitrile group from water solvation and induced yield enhancements for the mono-reacted compounds. We also reported the self-assembly of water-soluble metallocage featuring two endohedral polar binding sites. We showed that the efficient assembly of the metallcage requires the encapsulation of neutral mono-and ditopic polar guests. The assembled metallocage displayed conformational selectivity in the binding of aliphatic bis-formamides having different methylene spacers. Finally, we described the synthesis of an unprecedented tetra-oxazolo[4,5-b]pyrazinyl SAE-C[4]P ligand. We reported the self-assembly of a bis-metallocavitand based on the SAE-C[4]P ligand and Pt(II) precursors. Similarly, we showed that the inclusion of suitable polar guest was mandatory for the metallocavitand formation. The SAE-C[4]P ligand chelated only two Pt(II) metals between its adjacent substituents affordin

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Payton, John L. PhD. „The Photophysical Behavior of Aryl-diphosphenes and Aryl-phosphaalkenes: A Theoretical Study“. Cleveland, Ohio : Case Western Reserve University, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=case1270488297.

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Thesis (Doctor of Philosophy)--Case Western Reserve University, 2010
Department of Chemistry Title from PDF (viewed on 2010-05-25) Includes abstract Includes bibliographical references and appendices Available online via the OhioLINK ETD Center

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Chamoin, Sylvie. „Aryl-aryl Stille and Suzuzi-Miyaura cross-coupling reactions on solid support“. Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0022/NQ51184.pdf.

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Rydfjord, Jonas. „Palladium(II)-Catalyzed Addition Reactions : Synthesis of Aryl Amidines and Aryl Ketones“. Doctoral thesis, Uppsala universitet, Avdelningen för organisk farmaceutisk kemi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-326816.

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Palladium-catalyzed reactions have become one of the most important tools in modern organic chemistry due to its ability to catalyze the formation of new carbon-carbon bonds. The aim of the work presented in this thesis was to develop new palladium(II)-catalyzed addition reactions. In this work, cyanamides were investigated as a new substrate to give aryl amidines as products. The first protocol developed employed aryltrifluoroborates as the aryl partner, and the insertion of the aryl group into un-, mono-, and di-substituted cyanamides was successful for a wide variety of aryltrifluoroborates. An alternative method of generating the necessary intermediate for insertion into the cyanamide is the decarboxylative formation of aryl-palladium from aryl carboxylic acids. A protocol was developed for this reaction, but was unfortunately limited to a small number of ortho-substituted electron-rich aryl carboxylic acids. The mechanism was investigated by the means of DFT calculations and ESI-MS studies, and the rate-determining step was suggested to be the 1,2-carbopalladation based upon those results. A translation of the batch protocol to continuous-flow conditions was also demonstrated. The ideal method of generating the aryl-palladium species is by C-H bond activation, and this approach was demonstrated with indoles, giving a variety of 3-amidinoindoles as products. The mechanism was investigated by DFT calculations and a plausible catalytic cycle was proposed. A continuous-flow application of a desulfitative palladium(II)-catalyzed addition to nitriles to give ketones was developed. In addition, different reactor materials were evaluated in the microwave heated reactor cavity. Thus the reaction was shown to proceed with microwave heating in a borosilicate glass and an aluminum oxide reactor, and also in conditions mimicking conventional heating in a silicon carbide reactor. Finally, a protocol was developed for the convenient synthesis of sodium aryl sulfinates from Grignard and lithium reagents using a solid sulfur dioxide source as a safe alternative to the gas. The products of this protocol can be used as aryl-palladium precursors by a desulfitative process.

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Mei, Hua. „Perfluoroalkyl (aryl) sulfonimide zwitterions“. Connect to this title online, 2006. http://etd.lib.clemson.edu/documents/1175185494/.

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Bücher zum Thema "Aryl Y"

Chehimi, Mohamed Mehdi, Hrsg. Aryl Diazonium Salts. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.

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Singh, Sacha U. N. Aryl hydrocarbon-mediated inhibition of osteogenesis: Reversal by resveratrol, a novel aryl hydrocarbon receptor antagonist. [Toronto: University of Toronto, Faculty of Dentistry], 1999.

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Chehimi, Mohamed M., Jean Pinson und Fatima Mousli, Hrsg. Aryl Diazonium Salts and Related Compounds. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7.

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Atkinson, Jonathan Richard. Thermal & mechanical analysis of poly(aryl) systems. Birmingham: University of Birmingham, 1998.

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Cook, Robert Stephen Thomas. Chemical modification of poly(aryl ether sulphones). Birmingham: University of Birmingham, 1992.

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Kemmish, David John. Structure-property relationships in poly (aryl ether ether ketone), poly (aryl ether ketone) and some epoxy basedpaint systems. Birmingham: University of Birmingham, 1985.

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Darwen, Stuart. Synthetic and kinetic studies on some aryl azides. Salford: University of Salford, 1989.

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Owen, David Alan. Aryl substituted cyclohexadienyl iron complexes in alkaloid synthesis. Norwich: University of East Anglia, 1990.

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Tays, Kevin. Aryl hydroxamic acid analogues as potential therapeutic agents. St. Catharines, Ont: Brock University, Dept. of Chemistry, 1997.

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Henderson, Colin M. Nucleophilic additions to C-aryl, N-arylsulphonyl methyleneimines. [S.l: The Author], 1992.

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Buchteile zum Thema "Aryl Y"

Gooch, Jan W. „Aryl“. In Encyclopedic Dictionary of Polymers, 49. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_812.

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Schomburg, Dietmar, und Margit Salzmann. „Aryl acylamidase“. In Enzyme Handbook 4, 709–12. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-84437-9_131.

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Schomburg, Dietmar, und Dörte Stephan. „Aryl sulfotransferase“. In Enzyme Handbook, 907–14. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59025-2_168.

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Pinson, Jean. „Attachment of Organic Layers to Materials Surfaces by Reduction of Diazonium Salts“. In Aryl Diazonium Salts, 1–35. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch1.

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McCreery, Richard, und Adam Johan Bergren. „Diazonium Compounds in Molecular Electronics“. In Aryl Diazonium Salts, 219–39. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch10.

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Rappich, Jörg, Xin Zhang und Karsten Hinrichs. „Electronic Properties of Si Surfaces Modified by Aryl Diazonium Compounds“. In Aryl Diazonium Salts, 241–53. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch11.

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Podvorica, Fetah I. „Non-Diazonium Organic and Organometallic Coupling Agents for Surface Modification“. In Aryl Diazonium Salts, 255–81. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch12.

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Aswal, Dinesh K., Shankar Prasad Koiry und Shiv Kumar Gupta. „Various Electrochemical Strategies for Grafting Electronic Functional Molecules to Silicon“. In Aryl Diazonium Salts, 283–307. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch13.

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Belmont, James A., Christophe Bureau, Mohamed M. Chehimi, Sarra Gam-Derouich und Jean Pinson. „Patents and Industrial Applications of Aryl Diazonium Salts and Other Coupling Agents“. In Aryl Diazonium Salts, 309–21. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch14.

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Shao, Nan, Sheng Dai und De-en Jiang. „Aryl-Surface Bonding: A Density Functional Theory (DFT) Simulation Approach“. In Aryl Diazonium Salts, 37–52. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch2.

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Konferenzberichte zum Thema "Aryl Y"

Godoy Prieto, Leonela, Alicia Chopa und Maria Lockhart. „Tributylstannyl Azide as Efficient Reagent in the Synthesis of Aryl Azides from Aryl Amines“. In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a049.

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Herbivo, Cyril, Alain Comel und Gilbert Kirsch. „Synthesis of New Aryl-thienyl-thiophenes“. In The 11th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01320.

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Nunes, Vanessa Lóren, (PG) Ingryd Cristina de Oliveira und Olga S. do Rêgo Barros. „Copper(I)-Senelenophene-2-carboxylate Catalyzed Cross- Coupling of Aryl or alkyl Thiols And Aryl Halides“. In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0177-1.

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Dufossé, Laurent. „Microbial aryl carotenoids as bioactive food ingredients“. In Foods: Bioactives, Processing, Quality and Nutrition. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/bpqn2013-01295.

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Kharche, Ajay, Sandeep Waghulde, Nilesh Gorde und Mohan Kale. „MICROWAVE ASSISTED SYNTHESIS OF 2-ARYL BENZIMIDAZOLE“. In The 24th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08475.

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Silva, Júlia Akiyama da, Leonardo De Boni, Alessandra Pazini und Jones Limberger. „Controlling Two Photon Brightness of Benzothiadiazol Derivatives Through Aggregation“. In Frontiers in Optics. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/fio.2022.jtu5a.56.

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Annotation:

Molecules containing benzothiadiazole moieties were photophysically characterized. The quantum yields of fluorescence ranged depending on the aryl-aryloxy substituted group and aggregation formation, it was unveiled brightness properties relationship with aggregation for application in bioprobes.

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Bieleń, W., und I. Matyasik. „Aryl Isoprenoids as Indicators of Photic Zone Anoxia“. In 29th International Meeting on Organic Geochemistry. European Association of Geoscientists & Engineers, 2019. http://dx.doi.org/10.3997/2214-4609.201902983.

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Forostyanko, Anna, Elena Vasileva und Irina Proskurina. „SYNTHESIS OF 5-(4’-NITROPHENYL)-3-ARYL-1,2,4-OXADIAZOLES“. In Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m758.aks-2019/222-226.

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Kottmann, Robert M., Thomas H. Thatcher, Elizabeth Lyda, Amali Epa, Richard P. Phipps und Patricia J. Sime. „Aryl Hydrocarbon Receptor Ligands Inhibit TGF² Induced Myofibroblast Differentiation“. In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a1930.

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Liu, Chang, Jing Zhu, Wei Huang, Jin Xu, Changgui Lu und Yiping Cui. „Quadratic nonlinear optical properties of N-aryl stilbazolium dyes“. In Nonlinear Optics: Technologies and Applications. SPIE, 2007. http://dx.doi.org/10.1117/12.757577.

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Berichte der Organisationen zum Thema "Aryl Y"

Schneider, D. A., D. A. Loy, B. M. Baugher, D. R. Wheeler, R. A. Assink, T. M. Alam und R. Saunders. Preparation and characterization of aryl-substituted polysilsesquioxanes. Office of Scientific and Technical Information (OSTI), September 1998. http://dx.doi.org/10.2172/672121.

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Allcock, Harry R. Synthesis of Alkyl and Aryl Phosphazene High Polymers. Fort Belvoir, VA: Defense Technical Information Center, November 1990. http://dx.doi.org/10.21236/ada229369.

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Johnston, Randy F. Electron Density Modulation of Catalytic Metal Centers by Substituted Aryl-Isocyanide Ligands. Fort Belvoir, VA: Defense Technical Information Center, September 1989. http://dx.doi.org/10.21236/ada212875.

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Wynne, Shehla. Induction of the p75NTR by Aryl Propionic Acids in Prostate Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, Dezember 2008. http://dx.doi.org/10.21236/ada508209.

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Quann, Emily. Induction of the p75NTR by Aryl Propionic Acids in Prostate Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, Dezember 2007. http://dx.doi.org/10.21236/ada478245.

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Bedi, Vaibhav, Puja K. Mahajan und Nitin T. Patil. Gold Catalysis: A New Contender for Cross-Coupling Reactions with Aryl Halides. The Israel Chemical Society, März 2023. http://dx.doi.org/10.51167/acm00038.

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Carre, D. J., und P. A. Bertrand. Modeling and Measurement of Aryl Phosphate Ester Vapor Pressures at 50 Deg. C. Fort Belvoir, VA: Defense Technical Information Center, September 1998. http://dx.doi.org/10.21236/ada357652.

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Romagnolo, Donato F. A Molecular Model for Repression of BRCA-1 Transcription by the Aryl Hydrocarbon Receptor. Fort Belvoir, VA: Defense Technical Information Center, Juli 2002. http://dx.doi.org/10.21236/ada408088.

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Sherr, David H. The Aryl Hydrocarbon (Dioxin) Receptor/Transcription Factor and Cytochrome P450 1B1 as Targets for Breast Cancer Immunotherapy. Fort Belvoir, VA: Defense Technical Information Center, September 2002. http://dx.doi.org/10.21236/ada413137.

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