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Artykuły w czasopismach na temat "Aryl Y"
Wang, Xi-Cun, Fang Wang, Zheng-Jun Quan, Man-Gang Wang i 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 (listopad 2005): 689–90. http://dx.doi.org/10.3184/030823405774909423.
Pełny tekst źródłaSteparuk, Elena V., Dmitrii L. Obydennov i 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.
Pełny tekst źródłaYing, Jun, Zhengjie Le, Zhi-Peng Bao i 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.
Pełny tekst źródłaPassananti, Monica, Flavio Cermola, Marina DellaGreca, Maria Rosaria Iesce, Lucio Previtera, Rosalia Sferruzza i 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.
Pełny tekst źródłaJugelt, W. "Über Aryl-aroyl-diazomethane". Zeitschrift für Chemie 5, nr 12 (2.09.2010): 455–56. http://dx.doi.org/10.1002/zfch.19650051206.
Pełny tekst źródłaMkrtchyan, Satenik, Michał Jakubczyk, Suneel Lanka, Michael Pittelkow i 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.
Pełny tekst źródłaBhaskar Reddy, Dandu, Biradavolu Seenaiah, Adivireddi Padmaja i 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.
Pełny tekst źródłaRasheed, O. K., I. R. Hardcastle, J. Raftery i 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.
Pełny tekst źródłaGlaum, Marcus, Wolfgang Kläaui, Brian W. Skelton i 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.
Pełny tekst źródłaQuesnel, Jeffrey S., Alexander Fabrikant i 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.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaBarman, 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.
Pełny tekst źródłaZhou, 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.
Pełny tekst źródłaGramberg, 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.
Pełny tekst źródłaLeyva-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.
Pełny tekst źródłaSun, 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.
Pełny tekst źródłaEsta 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
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.
Pełny tekst źródłaDepartment of Chemistry Title from PDF (viewed on 2010-05-25) Includes abstract Includes bibliographical references and appendices Available online via the OhioLINK ETD Center
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.
Pełny tekst źródłaRydfjord, 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.
Pełny tekst źródłaMei, Hua. "Perfluoroalkyl (aryl) sulfonimide zwitterions". Connect to this title online, 2006. http://etd.lib.clemson.edu/documents/1175185494/.
Pełny tekst źródłaKsiążki na temat "Aryl Y"
Chehimi, Mohamed Mehdi, red. Aryl Diazonium Salts. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.
Pełny tekst źródłaSingh, 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.
Znajdź pełny tekst źródłaChehimi, Mohamed M., Jean Pinson i Fatima Mousli, red. Aryl Diazonium Salts and Related Compounds. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-04398-7.
Pełny tekst źródłaAtkinson, Jonathan Richard. Thermal & mechanical analysis of poly(aryl) systems. Birmingham: University of Birmingham, 1998.
Znajdź pełny tekst źródłaCook, Robert Stephen Thomas. Chemical modification of poly(aryl ether sulphones). Birmingham: University of Birmingham, 1992.
Znajdź pełny tekst źródłaKemmish, 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.
Znajdź pełny tekst źródłaDarwen, Stuart. Synthetic and kinetic studies on some aryl azides. Salford: University of Salford, 1989.
Znajdź pełny tekst źródłaOwen, David Alan. Aryl substituted cyclohexadienyl iron complexes in alkaloid synthesis. Norwich: University of East Anglia, 1990.
Znajdź pełny tekst źródłaTays, Kevin. Aryl hydroxamic acid analogues as potential therapeutic agents. St. Catharines, Ont: Brock University, Dept. of Chemistry, 1997.
Znajdź pełny tekst źródłaHenderson, Colin M. Nucleophilic additions to C-aryl, N-arylsulphonyl methyleneimines. [S.l: The Author], 1992.
Znajdź pełny tekst źródłaCzęści książek na temat "Aryl Y"
Gooch, Jan W. "Aryl". W Encyclopedic Dictionary of Polymers, 49. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_812.
Pełny tekst źródłaSchomburg, Dietmar, i Margit Salzmann. "Aryl acylamidase". W Enzyme Handbook 4, 709–12. Berlin, Heidelberg: Springer Berlin Heidelberg, 1991. http://dx.doi.org/10.1007/978-3-642-84437-9_131.
Pełny tekst źródłaSchomburg, Dietmar, i Dörte Stephan. "Aryl sulfotransferase". W Enzyme Handbook, 907–14. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59025-2_168.
Pełny tekst źródłaPinson, Jean. "Attachment of Organic Layers to Materials Surfaces by Reduction of Diazonium Salts". W Aryl Diazonium Salts, 1–35. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch1.
Pełny tekst źródłaMcCreery, Richard, i Adam Johan Bergren. "Diazonium Compounds in Molecular Electronics". W Aryl Diazonium Salts, 219–39. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch10.
Pełny tekst źródłaRappich, Jörg, Xin Zhang i Karsten Hinrichs. "Electronic Properties of Si Surfaces Modified by Aryl Diazonium Compounds". W Aryl Diazonium Salts, 241–53. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch11.
Pełny tekst źródłaPodvorica, Fetah I. "Non-Diazonium Organic and Organometallic Coupling Agents for Surface Modification". W Aryl Diazonium Salts, 255–81. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch12.
Pełny tekst źródłaAswal, Dinesh K., Shankar Prasad Koiry i Shiv Kumar Gupta. "Various Electrochemical Strategies for Grafting Electronic Functional Molecules to Silicon". W Aryl Diazonium Salts, 283–307. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch13.
Pełny tekst źródłaBelmont, James A., Christophe Bureau, Mohamed M. Chehimi, Sarra Gam-Derouich i Jean Pinson. "Patents and Industrial Applications of Aryl Diazonium Salts and Other Coupling Agents". W Aryl Diazonium Salts, 309–21. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch14.
Pełny tekst źródłaShao, Nan, Sheng Dai i De-en Jiang. "Aryl-Surface Bonding: A Density Functional Theory (DFT) Simulation Approach". W Aryl Diazonium Salts, 37–52. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527650446.ch2.
Pełny tekst źródłaStreszczenia konferencji na temat "Aryl Y"
Godoy Prieto, Leonela, Alicia Chopa i Maria Lockhart. "Tributylstannyl Azide as Efficient Reagent in the Synthesis of Aryl Azides from Aryl Amines". W The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-a049.
Pełny tekst źródłaHerbivo, Cyril, Alain Comel i Gilbert Kirsch. "Synthesis of New Aryl-thienyl-thiophenes". W The 11th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2007. http://dx.doi.org/10.3390/ecsoc-11-01320.
Pełny tekst źródłaNunes, Vanessa Lóren, (PG) Ingryd Cristina de Oliveira i Olga S. do Rêgo Barros. "Copper(I)-Senelenophene-2-carboxylate Catalyzed Cross- Coupling of Aryl or alkyl Thiols And Aryl Halides". W 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0177-1.
Pełny tekst źródłaDufossé, Laurent. "Microbial aryl carotenoids as bioactive food ingredients". W Foods: Bioactives, Processing, Quality and Nutrition. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/bpqn2013-01295.
Pełny tekst źródłaKharche, Ajay, Sandeep Waghulde, Nilesh Gorde i Mohan Kale. "MICROWAVE ASSISTED SYNTHESIS OF 2-ARYL BENZIMIDAZOLE". W The 24th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/ecsoc-24-08475.
Pełny tekst źródłaSilva, Júlia Akiyama da, Leonardo De Boni, Alessandra Pazini i Jones Limberger. "Controlling Two Photon Brightness of Benzothiadiazol Derivatives Through Aggregation". W Frontiers in Optics. Washington, D.C.: Optica Publishing Group, 2022. http://dx.doi.org/10.1364/fio.2022.jtu5a.56.
Pełny tekst źródłaBieleń, W., i I. Matyasik. "Aryl Isoprenoids as Indicators of Photic Zone Anoxia". W 29th International Meeting on Organic Geochemistry. European Association of Geoscientists & Engineers, 2019. http://dx.doi.org/10.3997/2214-4609.201902983.
Pełny tekst źródłaForostyanko, Anna, Elena Vasileva i Irina Proskurina. "SYNTHESIS OF 5-(4’-NITROPHENYL)-3-ARYL-1,2,4-OXADIAZOLES". W Chemistry of nitro compounds and related nitrogen-oxygen systems. LLC MAKS Press, 2019. http://dx.doi.org/10.29003/m758.aks-2019/222-226.
Pełny tekst źródłaKottmann, Robert M., Thomas H. Thatcher, Elizabeth Lyda, Amali Epa, Richard P. Phipps i Patricia J. Sime. "Aryl Hydrocarbon Receptor Ligands Inhibit TGF² Induced Myofibroblast Differentiation". W 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.
Pełny tekst źródłaLiu, Chang, Jing Zhu, Wei Huang, Jin Xu, Changgui Lu i Yiping Cui. "Quadratic nonlinear optical properties of N-aryl stilbazolium dyes". W Nonlinear Optics: Technologies and Applications. SPIE, 2007. http://dx.doi.org/10.1117/12.757577.
Pełny tekst źródłaRaporty organizacyjne na temat "Aryl Y"
Schneider, D. A., D. A. Loy, B. M. Baugher, D. R. Wheeler, R. A. Assink, T. M. Alam i R. Saunders. Preparation and characterization of aryl-substituted polysilsesquioxanes. Office of Scientific and Technical Information (OSTI), wrzesień 1998. http://dx.doi.org/10.2172/672121.
Pełny tekst źródłaAllcock, Harry R. Synthesis of Alkyl and Aryl Phosphazene High Polymers. Fort Belvoir, VA: Defense Technical Information Center, listopad 1990. http://dx.doi.org/10.21236/ada229369.
Pełny tekst źródłaJohnston, Randy F. Electron Density Modulation of Catalytic Metal Centers by Substituted Aryl-Isocyanide Ligands. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 1989. http://dx.doi.org/10.21236/ada212875.
Pełny tekst źródłaWynne, Shehla. Induction of the p75NTR by Aryl Propionic Acids in Prostate Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, grudzień 2008. http://dx.doi.org/10.21236/ada508209.
Pełny tekst źródłaQuann, Emily. Induction of the p75NTR by Aryl Propionic Acids in Prostate Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, grudzień 2007. http://dx.doi.org/10.21236/ada478245.
Pełny tekst źródłaBedi, Vaibhav, Puja K. Mahajan i Nitin T. Patil. Gold Catalysis: A New Contender for Cross-Coupling Reactions with Aryl Halides. The Israel Chemical Society, marzec 2023. http://dx.doi.org/10.51167/acm00038.
Pełny tekst źródłaCarre, D. J., i P. A. Bertrand. Modeling and Measurement of Aryl Phosphate Ester Vapor Pressures at 50 Deg. C. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 1998. http://dx.doi.org/10.21236/ada357652.
Pełny tekst źródłaRomagnolo, Donato F. A Molecular Model for Repression of BRCA-1 Transcription by the Aryl Hydrocarbon Receptor. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2002. http://dx.doi.org/10.21236/ada408088.
Pełny tekst źródłaRomagnolo, Donato F. A Molecular Model for Repression of BRCA-1 Transcription by the Aryl Hydrocarbon Receptor. Fort Belvoir, VA: Defense Technical Information Center, lipiec 2003. http://dx.doi.org/10.21236/ada418719.
Pełny tekst źródłaSherr, 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, wrzesień 2002. http://dx.doi.org/10.21236/ada413137.
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