Bibliografie tematiche / Organic compounds Synthesis

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Letteratura scientifica selezionata sul tema "Organic compounds Synthesis"

Autore: Grafiati
Pubblicato: 4 giugno 2021
Ultima modifica: 30 luglio 2024

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Articoli di riviste sul tema "Organic compounds Synthesis"

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Ariefin, Mokhamat, and Vety Sri Harlinda Ayudha. "Synthesis and Characterization of Benzodithiophene (BDT) Quinoid Compounds as a Potential Compound for n-Type Organic Thin-Film Transistors (OTFT)." Jurnal Kimia Sains dan Aplikasi 23, no. 7 (July 17, 2020): 261–66. http://dx.doi.org/10.14710/jksa.23.7.261-266.

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Two potential compounds as an n-Type organic thin-film transistor (OTFT) from benzodithiophene (BDT) derivatives have been synthesized and characterized. BDT was chosen as the core because it has π-conjugated bonds, rigid structures, and planar. Quinoid structure with end-cap (terminal group) in the form of dicyanomethylene is used because it can lower the LUMO value of the compound, and side chains are selected in the form of alkoxy so that two BDT derivatives are obtained namely BDTQ-6 (hexyloxy) and BDTQ-10 (decyloxy). Based on the results of TGA, BDTQ-6 and BDTQ-10 have decomposition point
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Lobzhanidze, Tea. "Synthesis, Study and Use of New Type Biologically Active Arsenic-Organic Complex Compounds." Chemistry & Chemical Technology 6, no. 4 (December 20, 2012): 371–76. http://dx.doi.org/10.23939/chcht06.04.371.

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MURAHASHI, Shun-Ichi, and Takeshi NAOTA. "Organic synthesis using ruthenium compounds." Journal of Synthetic Organic Chemistry, Japan 46, no. 10 (1988): 930–42. http://dx.doi.org/10.5059/yukigoseikyokaishi.46.930.

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KUSAMA, Hiroyuki, and Koichi NARASAKA. "Rhenium Compounds in Organic Synthesis." Journal of Synthetic Organic Chemistry, Japan 54, no. 8 (1996): 644–53. http://dx.doi.org/10.5059/yukigoseikyokaishi.54.644.

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SHINOKUBO, Hiroshi, and Koichiro OSHIMA. "Organic Synthesis Using Organomanganese Compounds." Journal of Synthetic Organic Chemistry, Japan 57, no. 1 (1999): 13–23. http://dx.doi.org/10.5059/yukigoseikyokaishi.57.13.

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Negishi, Ei-ichi, and Tamotsu Takahashi. "Organozirconium Compounds in Organic Synthesis." Synthesis 1988, no. 01 (1988): 1–19. http://dx.doi.org/10.1055/s-1988-27453.

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Sadekov, Igor D., B. B. Rivkin, and Vladimir I. Minkin. "Organotellurium Compounds in Organic Synthesis." Russian Chemical Reviews 56, no. 4 (April 30, 1987): 343–54. http://dx.doi.org/10.1070/rc1987v056n04abeh003275.

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Khusnutdinov, R. I., T. M. Oshnyakova, and U. M. Dzhemilev. "Molybdenum compounds in organic synthesis." Russian Chemical Reviews 86, no. 2 (February 28, 2017): 128–63. http://dx.doi.org/10.1070/rcr4617.

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Jiao, Jiao, and Yasushi Nishihara. "Alkynylboron compounds in organic synthesis." Journal of Organometallic Chemistry 721-722 (December 2012): 3–16. http://dx.doi.org/10.1016/j.jorganchem.2012.05.027.

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Knölker, H. J. "Iron Compounds in Organic Synthesis." Synthesis 1994, no. 10 (1994): 1106. http://dx.doi.org/10.1055/s-1994-25646.

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Tesi sul tema "Organic compounds Synthesis"

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Newington, Ian M. "Azo-anions in organic synthesis." Thesis, University of Oxford, 1985. http://ora.ox.ac.uk/objects/uuid:690ab891-be13-4582-a029-47974d20adac.

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Novel synthetic applications of ambident azo-anions derived from hindered hydrazones have been investigated. Reaction with electrophiles occurred predominantly at carbon as the N-addition pathway was sterically retarded. Trityl, diphenyl-4-pyridylmethyl (DPP) benzhydryl, and t-butyldiphenylmethyl (BDP) hydrazones of various aldehydes and ketones were prepared in good yields from the corresponding hydrazines and carbonyls in aqueous methanol. The lithium salts derived from trityl and DPP hydrazones, by treatment with methyl lithium at -55°C, reacted with aldehydes and ketones to generate azo-al
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Esfandiarfard, Keyhan. "Novel Organophosphorus Compounds for Materials and Organic Synthesis." Doctoral thesis, Uppsala universitet, Molekylär biomimetik, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-328295.

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This thesis is devoted to the development of new organophosphorus compounds for potential uses in material science and as reagents in Organic Chemistry. Organophosphorus compounds in a single molecule or organic electronics context are appealing as the phosphorous centers perturb the electronic properties of the π-conjugated systems while at the same time provide synthetic handles for subsequent synthetic modifications. As such, new synthetic methodology to such compounds and the exploration of new building blocks is of considerable interest. In a different study, novel organophosphorus compou
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Reynolds, Stephen J. "Carbamoylcobalt (III) compounds in organic synthesis." Thesis, University of Nottingham, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.280294.

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This thesis describes the development and use of organocobalt (III) compounds in the formation of carbon-carbon and carbon-heteroatom bonds and, in particular, details the application of this chemistry for the synthesis of functionalised amides and ~, 1" and 8-lactams. Organocobalt chemistry was born from the isolation and characterisation of the vitamin B12 coenzyme (2) in the 1950s and early 1960s. The introduction to this thesis covers the search for vitamin B12 and briefly describes its biological role. Next, the considerable development of the simple vitamin B12 analogues, i.e. organocoba
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Kim, Byeongmoon 1957. "Asymmetric organic synthesis using organoboron compounds." Thesis, Massachusetts Institute of Technology, 1987. http://hdl.handle.net/1721.1/14679.

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Sharma, Y. "Continuous flow synthesis of organic compounds." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2017. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/4520.

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Haughey, Simon Anthony. "Chemoenzymatic synthesis of organosulfur compounds." Thesis, Queen's University Belfast, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318731.

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Kou, Xiaodi. "Synthesis, characterization and reactivity of organic bismuth compounds." Fort Worth, Tex. : Texas Christian University, 2007. http://etd.tcu.edu/etdfiles/available/etd-07312007-125631/unrestricted/kou.pdf.

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Wallner, Olov. "Palladium-Catalyzed Synthesis and Transformations of Organometallic Compounds." Doctoral thesis, Stockholm : Dept. of Organic Chemistry, Stockholm University, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-804.

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Wang, Haofan. "Synthesis and reactions of organoiron compounds." Diss., The University of Arizona, 2003. http://hdl.handle.net/10150/289994.

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The multistep synthesis of the redox active adenine analog [e]-ferrocenyl-4-aminopyrimidine is reported. The redox active system will be incorporated into oligonucleotides to study the electron transfer through the molecular pi-system of DNA in future studies. Attempts were made to synthesize a cyclopenta-4-aminopyrimidine derivative which possesses an endocyclic double bond in the cyclopentane ring. This intermediate can be subsequently coupled with cyclopentadienyl iron dicarbonyl (Fp) group and, after thermal decarbonylation, form the desired ferrocene ring. Many double bond precursors are
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Buckley, Anne Margaret. "Inorganic-organic layer compounds : synthesis and properties." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.253398.

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Libri sul tema "Organic compounds Synthesis"

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Hans-Günther, Schmalz, and Wirth Thomas 1964-, eds. Organic synthesis highlights V. Weinheim: Wiley-VCH, 2003.

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Willis, Christine L. Organic synthesis. Oxford: Oxford University Press, 1995.

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M, Trost Barry, and International Union of Pure and Applied Chemistry., eds. Stereocontrolled organic synthesis. Oxford: Blackwell Scientific Publications, 1994.

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Smith, Michael B. Organic synthesis. New York: McGraw-Hill, 1994.

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J, Mulzer, and Waldmann H, eds. Organic synthesis highlights III. Weinheim: Wiley-VCH, 1998.

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Tanaka, Koichi. Solvent-free organic synthesis. Weinheim: Wiley-VCH, 2003.

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Ahluwalia, V. K. Organic synthesis: Special techniques. Pangbourne: Alpha Science International, 2001.

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Ho, Tse-Lok. Tactics of organic synthesis. New York: Wiley, 1994.

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Hanson, James Ralph. Organic synthetic methods. New York: Wiley-Interscience, 2002.

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Larock, Richard C. Organomercury Compounds in Organic Synthesis. Berlin, Heidelberg: Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-642-70004-0.

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Capitoli di libri sul tema "Organic compounds Synthesis"

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Ahluwalia, V. K. "Stereoselective Synthesis." In Stereochemistry of Organic Compounds, 505–61. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-84961-0_18.

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Volke, Jiří, and František Liška. "Reactions of Organic Compounds at Electrodes." In Electrochemistry in Organic Synthesis, 45–139. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78699-0_3.

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Fagnoni, Maurizio. "CHAPTER 6. Colored Compounds for Eco-sustainable Visible-light Promoted Syntheses." In Sustainable Organic Synthesis, 150–80. Cambridge: Royal Society of Chemistry, 2021. http://dx.doi.org/10.1039/9781839164842-00150.

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Norman, Richard, and James M. Coxon. "The syntheses of some naturally occurring compounds." In Principles of Organic Synthesis, 728–90. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2166-8_22.

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Ahluwalia, V. K. "Reduction of Specific Types of Organic Compounds." In Reduction in Organic Synthesis, 55–113. Cham: Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-37686-3_3.

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Norman, Richard, and James M. Coxon. "The synthesis of five-and six-membered heterocyclic compounds." In Principles of Organic Synthesis, 676–727. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2166-8_21.

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Carl, Elena, and Dietmar Stalke. "Structure-Reactivity Relationship in Organolithium Compounds." In Lithium Compounds in Organic Synthesis, 1–32. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch1.

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Shimizu, Masaki. "Lithium Compounds in Cross-Coupling Reactions." In Lithium Compounds in Organic Synthesis, 463–90. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.ch16.

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Liang, Huan, and Marco A. Ciufolini. "Biomimetic Synthesis of Alkaloids Derived from Tyrosine: The Case of FR-901483 and TAN-1251 Compounds." In Biomimetic Organic Synthesis, 61–89. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2011. http://dx.doi.org/10.1002/9783527634606.ch2.

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Brunner, Henri. "Enantioselective Synthesis of Organic Compounds with Optically Active Transition Metal Catalysts and Transition Metal Compounds." In Organometallics in Organic Synthesis 2, 277–89. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-74269-9_15.

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Atti di convegni sul tema "Organic compounds Synthesis"

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Monçalves, Matias, Mariana M. Bassaco, Marcos A. Villetti, and Claudio C. Silveira. "Novel Divinyl Sulfides: Potential Luminescent Compounds." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0308-1.

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Martins, Lucimara J., Wanessa F. Altei, Cristiane S. Schwalm, Adriano D. Andricopulo, and Fernando Coelho. "Synthesis of new biologically actived azaspiro compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013917144424.

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Ali, Bakhat, Hélio A. Stefani, and Fernando P. Ferreira. "Addition of Amino Acids to oxopyrrolidin compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_20131014161751.

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Silva, Anderson B. da, and Juliana A. Vale. "Rapid synthesis of di-1,2,4-oxadiazoles pyridyl compounds." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0031-1.

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Silva, Anderson B. da, and Juliana A. Vale. "Rapid synthesis of di-1,2,4-oxadiazoles pyridyl compounds." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0317-1.

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Carneiro, Paula F., Maria do Carmo F. R. Pinto, Tatiane S. Coelho, Antonio V. Pinto, Kelly C. G. Moura, Pedro A. da Silva, and Eufrânio N. da Silva Júnior. "Quinonoid and phenazine compounds: synthesis of new antimycobacterial prototypes." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0224-1.

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Barbosa, Flavio A. R., Rômulo F. S. Canto, and Antonio L. Braga. "Synthesis of novel 6-seleno-dihydropyrimidinones: Potentially bioactive compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013819222620.

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Rafique, Jamal, Sumbal Saba, Rômulo F. S. Canto, Waseem Hassan, João B. T. Rocha, and Antonio L. Braga. "Synthesis of Diselenide Based Picolylamide Derivatives: Biologically Potential Compounds." In 15th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_2013822125235.

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Valdomir, Guillermo, Juan Ignacio Padrón, Jenny Saldaña, José Manuel Padrón, Gloria Serra, Eduardo Manta, Victor S. Martín, and Danilo Davyt. "Synthesis of hybrids compounds by Click Chemistry and their bioactivities." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0081-1.

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Brondani, Patrícia B., Gonzalo de Gonzalo, Marco W. Fraaije, and Leandro H. Andrade. "Selective oxidations of organoboron compounds catalyzed by Baeyer-Villiger monooxygenases." In 14th Brazilian Meeting on Organic Synthesis. São Paulo: Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0097-2.

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Rapporti di organizzazioni sul tema "Organic compounds Synthesis"

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Singh, Anjali. Amino Acids: Building Blocks of Proteins. ConductScience, June 2022. http://dx.doi.org/10.55157/cs20220612.

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Amino acids are essential organic compounds serving as protein building blocks. Recognized for their biological roles, they underpin proteins' structure and interactions. Classified by polarity and nutritional necessity, essential amino acids, not synthesized by the body, include histidine, leucine, lysine, and more, while non-essential ones are produced internally. These molecules exhibit diverse functions, from neurotransmitter precursor synthesis to immune support. Industries leverage amino acids in animal feed, artificial sweeteners, flavor enhancers, and drug manufacturing, highlighting t
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Wiemers, K. D., H. Babad, R. T. Hallen, L. P. Jackson, and M. E. Lerchen. An Assessment of the Stability and the Potential for In-Situ Synthesis of Regulated Organic Compounds in High Level Radioactive Waste Stored at Hanford, Richland, Washington. Office of Scientific and Technical Information (OSTI), January 1999. http://dx.doi.org/10.2172/2535.

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Jung, Carina, Karl Indest, Matthew Carr, Richard Lance, Lyndsay Carrigee, and Kayla Clark. Properties and detectability of rogue synthetic biology (SynBio) products in complex matrices. Engineer Research and Development Center (U.S.), September 2022. http://dx.doi.org/10.21079/11681/45345.

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Synthetic biology (SynBio) aims to rationally engineer or modify traits of an organism or integrate the behaviors of multiple organisms into a singular functional organism through advanced genetic engineering techniques. One objective of this research was to determine the environmental persistence of engineered DNA in the environment. To accomplish this goal, the environmental persistence of legacy engineered DNA building blocks were targeted that laid the foundation for SynBio product development and application giving rise to “post-use products.” These building blocks include genetic constru
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Chefetz, Benny, and Baoshan Xing. Sorption of hydrophobic pesticides to aliphatic components of soil organic matter. United States Department of Agriculture, 2003. http://dx.doi.org/10.32747/2003.7587241.bard.

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Sorption of hydrophobic compounds to aliphatic components of soil organic matter (SOM) is poorly understood even though these aliphatic carbons are a major fraction of SOM. The main source of aliphatic compounds in SOM is above- and below-ground plant cuticular materials (cutin, cutan and suberin). As decomposition proceeds, these aliphatic moieties tend to accumulate in soils. Therefore, if we consider that cuticular material contributes significantly to SOM, we can hypothesize that the cuticular materials play an important role in the sorption processes of hydrophobic compounds (including pe
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Zhirov, Nikita, Akim Akimov, and Sergei Zhuravkov. Synthesis and properties of bicomponent complex systems based on organic acid and polyoxometalate compound. Peeref, July 2023. http://dx.doi.org/10.54985/peeref.2307p9790614.

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Sisler, Edward C., Raphael Goren, and Akiva Apelbaum. Controlling Ethylene Responses in Horticultural Crops at the Receptor Level. United States Department of Agriculture, October 2001. http://dx.doi.org/10.32747/2001.7580668.bard.

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Ethylene is a plant hormone that controls many plant responses, such as growth, senescence, ripening, abscission and seed germination. Recently, 1-methy- cyclopropene (1-MCP), was shown to bind to ethylene receptor for a certain period of time and prevent ethylene action. The objectives of this research were to synthesize analogues of 1-MCP and test their potency to block the ethylene receptor and inhibit ethylene action. During the course of this project, procedures for synthesis and shipment of the cyclopropene compounds were developed as well assay procedures for each compound were worked o
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Amir, Rachel, David J. Oliver, Gad Galili, and Jacline V. Shanks. The Role of Cysteine Partitioning into Glutathione and Methionine Synthesis During Normal and Stress Conditions. United States Department of Agriculture, January 2013. http://dx.doi.org/10.32747/2013.7699850.bard.

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The objective of this research is to study the nature of the competition for cysteine (Cys), the first organic sulfur-containing compound, between its two main metabolites, glutathione (GSH) and methionine (Met). GSH plays a central role in protecting plants during various stresses, while Met, an essential amino acid, regulates essential processes and metabolites in plant cells through its metabolite S-adenosyl-Met. Our results, which are based on flux analysis and measurements of Met- metabolites, show that the flux towards Met synthesis is high during non-stress conditions, however the flux
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Corscadden, Louise, and Anjali Singh. Metabolism And Measurable Metabolic Parameters. ConductScience, December 2022. http://dx.doi.org/10.55157/me20221213.

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Metabolism is the sum of chemical reactions involved in sustaining the life of organisms.[1] It constantly provides your body with the energy to perform essential functions. The process is categorized into two groups:[2] Catabolism: It’s the process of breaking down molecules to obtain energy. For example, converting glucose to pyruvate by cellular respiration. Anabolism: It’s the process of synthesis of compounds required to run the metabolic process of the organisms. For example, carbohydrates, proteins, lipids, and nucleic acids.[2] Metabolism is affected by a range of factors, such as age,
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Trace elements and synthetic organic compounds in biota and streambed sediment of the Western Lake Michigan Drainages, 1992-1995. US Geological Survey, 1997. http://dx.doi.org/10.3133/wri974192.

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Synthetic organic compounds and carp endocrinology and histology in Las Vegas Wash and Las Vegas and Callville Bays of Lake Mead, Nevada, 1992 and 1995. US Geological Survey, 1996. http://dx.doi.org/10.3133/wri964266.

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