Добірка наукової літератури з теми "Synthesis of thioamide"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Synthesis of thioamide".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Synthesis of thioamide"
Dong, Zhi-Bing, Meng-Tian Zeng, Min Wang, Han-Ying Peng, and Yu Cheng. "Copper-Catalyzed Synthesis of Aryl Thioamides from Aryl Aldehydes and Tetramethylthiuram Disulfide." Synthesis 50, no. 03 (October 12, 2017): 644–50. http://dx.doi.org/10.1055/s-0036-1590936.
Повний текст джерелаSauvé, Gilles, Vanga S. Rao, Gilles Lajoie, and Bernard Belleau. "Backbone-modified oligopeptidic bioregulators. The synthesis and configuration of thioamide, amidoxime, cyanoamidine, and amidrazone analogs of the chemotactic peptide N-formyl-methionyl-leucyl-phenylalanine (f-Met-Leu-Phe-OR)." Canadian Journal of Chemistry 63, no. 11 (November 1, 1985): 3089–101. http://dx.doi.org/10.1139/v85-511.
Повний текст джерелаFong, Mei, Wit K. Janowski, Rolf H. Prager, and Max R. Taylor. "A Convenient Synthesis of 2-Substituted Thiazole-5-carboxylates." Australian Journal of Chemistry 57, no. 6 (2004): 599. http://dx.doi.org/10.1071/ch03252.
Повний текст джерелаSzantai-Kis, D., Christopher Walters, Taylor Barrett, Eileen Hoang, and E. Petersson. "Thieme Chemistry Journals Awardees – Where Are They Now? Improved Fmoc Deprotection Methods for the Synthesis of Thioamide-Containing Peptides and Proteins." Synlett 28, no. 14 (May 19, 2017): 1789–94. http://dx.doi.org/10.1055/s-0036-1589027.
Повний текст джерелаZhang, Qiang, Laurent Soulère, and Yves Queneau. "Towards More Practical Methods for the Chemical Synthesis of Thioamides Using Sulfuration Agents: A Decade Update." Molecules 28, no. 8 (April 17, 2023): 3527. http://dx.doi.org/10.3390/molecules28083527.
Повний текст джерелаPham Xuan Thao. "Study on the synthesis of thioamides from aldehyde N-tert-butylsulfinyl amide and sulfur in aqueous media." Journal of Military Science and Technology, no. 76 (December 12, 2021): 54–60. http://dx.doi.org/10.54939/1859-1043.j.mst.76.2021.54-60.
Повний текст джерелаHammam, A. S., and B. E. Bayoumy. "Reaction of thioamides with 2,3-dichloro-1,4-naphthoquinone. A novel synthesis of naphtho[2,3-d]thiazole-4,9-diones." Collection of Czechoslovak Chemical Communications 50, no. 1 (1985): 71–79. http://dx.doi.org/10.1135/cccc19850071.
Повний текст джерелаSharma, Shubham, Dharmender Singh, Sunit Kumar, Vaishali, Rahul Jamra, Naveen Banyal, Deepika, Chandi C. Malakar, and Virender Singh. "An efficient metal-free and catalyst-free C–S/C–O bond-formation strategy: synthesis of pyrazole-conjugated thioamides and amides." Beilstein Journal of Organic Chemistry 19 (March 2, 2023): 231–44. http://dx.doi.org/10.3762/bjoc.19.22.
Повний текст джерелаYeo, Chien, and Edward Tiekink. "O-Methyl m-Tolylcarbamothioate." Molbank 2018, no. 3 (September 15, 2018): M1020. http://dx.doi.org/10.3390/m1020.
Повний текст джерелаCakmak, M., I. I. Ozturk, C. N. Banti, M. Manoli, E. Moushi, A. J. Tasiopoulos, A. M. Grześkiewicz, M. Kubicki, and S. K. Hadjikakou. "Bismuth(III) bromide-thioamide complexes: synthesis, characterization and cytotoxic properties." Main Group Metal Chemistry 41, no. 5-6 (November 27, 2018): 143–54. http://dx.doi.org/10.1515/mgmc-2018-0035.
Повний текст джерелаДисертації з теми "Synthesis of thioamide"
Brandes, Dee Anne. "The synthesis and reactivity of alpha,beta-unsaturated thioamide, thioester, and thione iron tricarbonyl complexes." Thesis, University of Ottawa (Canada), 1990. http://hdl.handle.net/10393/6008.
Повний текст джерелаMukherjee, Suvodip. "Methodological approach on carbon-hetero bond formation reaction." Thesis, University of North Bengal, 2022. http://ir.nbu.ac.in/handle/123456789/4792.
Повний текст джерелаKienz, Torben [Verfasser]. "Exploration of N-ferrocenyl substituted thioamides : synthesis, properties and reactivity / Torben Kienz." Mainz : Universitätsbibliothek Mainz, 2016. http://d-nb.info/1120619912/34.
Повний текст джерелаEllwood, A. R. "A synthetic approach to the sarain core and development of new thioamide-based methodologies." Thesis, University College London (University of London), 2011. http://discovery.ucl.ac.uk/1332893/.
Повний текст джерелаLELONG, BRUNO. "Synthese diastereoselective de thioamides ' et -dihydroxyles : une voie d'acces aux valerolactones." Caen, 1997. http://www.theses.fr/1997CAEN2059.
Повний текст джерелаABOUSAID, LEKBIR. "Etude cinetique de la thioamidation en serie aromatique. Synthese et caracterisation des (co)polyamide-thioamides." Caen, 1996. http://www.theses.fr/1996CAEN2031.
Повний текст джерелаRodriguez-Garcia, Valerie. "Efficient methodology for the synthesis of 2,4-benzodiazepin-1-ones, sulfonylbenzotriazoles, sulfonamides, ethylene sulfonamides, thiocarbamates, dithiocarbamates and thioamides." [Gainesville, Fla.] : University of Florida, 2004. http://purl.fcla.edu/fcla/etd/UFE0006303.
Повний текст джерелаKulesza, Joanna. "Synthesis and studies of binding properties of calix[4]arenes functionalised with amide and hydroxamate moities and their thiocarbonyl analogues." Strasbourg, 2011. http://www.theses.fr/2011STRA6093.
Повний текст джерелаThe need of monitoring and controlling the concentration of heavy metal ions such as Pb2+ or Cd2+, which have toxic effects on all living organisms inspires chemists to synthesise more and more selective compounds. The aim of this work was the synthesis of amide and hydroxyamide derivatives of calix[4]arenes and their thiocarbonyl analogues. Nine thioamide derivatives as well as their respective amide derivatives, five hydroxamate derivatives and four calix[4]arene-hydroxamic acids were obtained. Studies of ligands interaction with metal cations were investigated using different techniques: 1H NMR spectroscopy, X-ray diffraction, liquid-liquid extraction, UV absorption spectrophotometry, potentiometry and microcalorimetry. The replacement of the oxygen atoms by sulphur atoms in the tertiary amide structures led to compounds highly selective for Ag+ and Pb2+ over I and II group of cations. Hydroxamic acids of calix[4]arene occurred to be efficient extractants for Fe3+ and Cu2+. Moreover, very important results obtained with these compounds could find an application in the context of the removal and separation of Pb2+ from other toxic metals such as Cd2+. In addition, these ligands could be used to separate Cu2+ from Ni2+ and Zn2+, which are often found together. Selectivity of thioamide and hydroxamate derivatives was assessed using these ligands as sensor materials in ion-selective membrane electrodes. Electrodes based on calix[4]arene-thioamides, particularly on compounds bearing piperidinyl and morpholinyl substituents are promising analytical tools for monitoring Pb2+ concentration in natural and drinking waters
Mykhaylychenko, Sergiy. "Study of perfluoroketene dithioacetals and N,S-acetals for the synthesis of fluorinated acyclic and heterocyclic compounds." Rouen, 2008. http://www.theses.fr/2008ROUES066.
Повний текст джерелаPerfluoroketene dithioacetals are simple and highly versatile building-blocks for the synthesis of various fluorinated acyclic and heterocyclic compounds. Efficient and straightforward transformation of a,b-unsaturated g-lactones into 2,2,2-trifluoroethyl substituted γ-lactams and pyridazin-3-ones was performed, starting from a variety of primary amines or hydrazines and perfluoroketene dithioacetatals. The structures of all new compounds were ascribed using NMR (19F, 1H, 13C), IR, MS data and X-ray diffraction analysis. The possible mechanisms for the formation of γ-lactams and pyridazin-3-ones are also presented. The reactions of N-monosubstituted polyfluorothioamides with alkyllithium reagents were studied. In the case of N,N-disubstituted perfluorothioamides N,S-acetals were obtained. Some chemical properties of perfluoroketene-N,S-acetals, including oxidation and chlorination reactions, were investigated. Oxidation reaction of perfluoroketene-N,S-acetals with t-butylhydroperoxide led to a formation of a-hydroperfluoroamides. Chlorination of perfluoroketene-N,S-acetals with sulfuryl chloride gave a-chloroperfluoroamides; this method proved to be a new approach in the synthesis of polyfluorinated a-chloro optically active compounds. The possible mechanisms for these transformations are discussed
Khatri, Bhavesh. "Exploring Nature's Inventory: Investigating the Role of Amide to Thioamide Substitution on Protein Stability." Thesis, 2020. https://etd.iisc.ac.in/handle/2005/5635.
Повний текст джерелаКниги з теми "Synthesis of thioamide"
Reilly, William Leo 1926. Some Reactions of Fluorocarbon Nitriles: Syntheses of Amidines, Thioamides and Triazines. Creative Media Partners, LLC, 2021.
Знайти повний текст джерелаЧастини книг з теми "Synthesis of thioamide"
Murai, Toshiaki. "Synthesis of Thioamides." In Chemistry of Thioamides, 45–73. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7828-7_3.
Повний текст джерелаKumagai, Naoya, and Masakatsu Shibasaki. "Asymmetric Synthesis Using Thioamides." In Chemistry of Thioamides, 103–25. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7828-7_5.
Повний текст джерелаYan, Hong, and Hai-Chao Xu. "Synthesis of Heterocycles from Thioamides." In Chemistry of Thioamides, 127–55. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7828-7_6.
Повний текст джерелаZhang, Xue, Jinhua Yang, and Junfeng Zhao. "Ynamide-Mediated Synthetic Approach to Thioamide-Substituted Peptides." In Methods in Molecular Biology, 69–80. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2489-0_6.
Повний текст джерелаKantlehner, W. "Synthesis from α-Phosphoryl Thioamide Derivatives." In Three Carbon-Heteroatom Bonds: Ketenes and Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00418.
Повний текст джерелаChou, Jonathan Chiu-Chun, Veronica E. Stafford, Grace E. Kenney, and Laura M. K. Dassama. "The enzymology of oxazolone and thioamide synthesis in methanobactin." In Synthetic and Enzymatic Modifications of the Peptide Backbone, 341–73. Elsevier, 2021. http://dx.doi.org/10.1016/bs.mie.2021.04.008.
Повний текст джерелаTaber, Douglass F. "Enantioselective Preparation of Alkylated Stereogenic Centers." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0042.
Повний текст джерелаTaber, Douglass F. "Stereocontrolled C-N Ring Construction: The Pyne Synthesis of Hyacinthacine B 3." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0054.
Повний текст джерелаTang, R. Y. "22.1.7.2 Thioamides (Update 2024)." In Knowledge Updates 2024/1. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-122-00021.
Повний текст джерелаBraverman, S., M. Cherkinsky, and M. L. Birsa. "Synthesis of Thioamides." In Four Carbon-Heteroatom Bonds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00203.
Повний текст джерелаТези доповідей конференцій з теми "Synthesis of thioamide"
Stojković, Danijela, Maja Đukić, Marija Ristić, Marina Ćendić Serafinović, Svetlana Belošević, Emina Mrkalić, and Ivan Jakovljević. "Synthesis, characterization and HSA interactions of a new piano-stool ruthenium(II) complex containing a thioamide-type ligand." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.507s.
Повний текст джерелаDekamin, Mohammad G., Niaz Kheirabi, and Zahra Karimi. "A green and facile ultrasound-promoted synthesis of thioamide derivatives catalyzed by Cu(I)@Chitosan as a new bio-polymeric nano catalyst in aqueous media." In The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a028.
Повний текст джерелаDotsenko, Victor, Konstantin Frolov, and Sergey Krivokolysko. "DMSO-HCl System as an Efficient Oxidant of Thioamides and Selenoamides." In The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01073.
Повний текст джерелаLevchenko, Arina G., Polina G. Dahno, and Victor V. Dotsenko. "Synthesis of N-(hydroxymethylene)thioamides by N-hydroxymethylation of 2-cyanothioacrylamides." In ECSOC-25. Basel Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11799.
Повний текст джерелаHeimgartner, Heinz, Jürg Lehmann, and Anthony Linden. "Site-Selective Incorporation of Thioamide-Linkages into a Growing Peptide via Variation of the 'Azirine/Oxazolone Method'." In The 1st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02033.
Повний текст джерелаMuntyan, Victoria S., Mariia E. Vladimirova, Alexey M. Afonin, Alexey N. Muntyan, and Marina L. Roumiantseva. "ANALYSIS OF SALT-SENSITIVE AND SALT-TOLERANT SINORHIZOBIUM MELILOTI STRAINS USING DNA MICROARRAY, PHENOTYPE MICROARRAY AND GENOME MINING TECHNIQUES." In 23rd SGEM International Multidisciplinary Scientific GeoConference 2023. STEF92 Technology, 2023. http://dx.doi.org/10.5593/sgem2023/6.1/s25.15.
Повний текст джерела