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Artykuły w czasopismach na temat "Synthesis of thioamide"
Dong, Zhi-Bing, Meng-Tian Zeng, Min Wang, Han-Ying Peng i Yu Cheng. "Copper-Catalyzed Synthesis of Aryl Thioamides from Aryl Aldehydes and Tetramethylthiuram Disulfide". Synthesis 50, nr 03 (12.10.2017): 644–50. http://dx.doi.org/10.1055/s-0036-1590936.
Pełny tekst źródłaSauvé, Gilles, Vanga S. Rao, Gilles Lajoie i 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, nr 11 (1.11.1985): 3089–101. http://dx.doi.org/10.1139/v85-511.
Pełny tekst źródłaFong, Mei, Wit K. Janowski, Rolf H. Prager i Max R. Taylor. "A Convenient Synthesis of 2-Substituted Thiazole-5-carboxylates". Australian Journal of Chemistry 57, nr 6 (2004): 599. http://dx.doi.org/10.1071/ch03252.
Pełny tekst źródłaSzantai-Kis, D., Christopher Walters, Taylor Barrett, Eileen Hoang i 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, nr 14 (19.05.2017): 1789–94. http://dx.doi.org/10.1055/s-0036-1589027.
Pełny tekst źródłaZhang, Qiang, Laurent Soulère i Yves Queneau. "Towards More Practical Methods for the Chemical Synthesis of Thioamides Using Sulfuration Agents: A Decade Update". Molecules 28, nr 8 (17.04.2023): 3527. http://dx.doi.org/10.3390/molecules28083527.
Pełny tekst źródłaPham 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, nr 76 (12.12.2021): 54–60. http://dx.doi.org/10.54939/1859-1043.j.mst.76.2021.54-60.
Pełny tekst źródłaHammam, A. S., i 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, nr 1 (1985): 71–79. http://dx.doi.org/10.1135/cccc19850071.
Pełny tekst źródłaSharma, Shubham, Dharmender Singh, Sunit Kumar, Vaishali, Rahul Jamra, Naveen Banyal, Deepika, Chandi C. Malakar i 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 (2.03.2023): 231–44. http://dx.doi.org/10.3762/bjoc.19.22.
Pełny tekst źródłaYeo, Chien, i Edward Tiekink. "O-Methyl m-Tolylcarbamothioate". Molbank 2018, nr 3 (15.09.2018): M1020. http://dx.doi.org/10.3390/m1020.
Pełny tekst źródłaCakmak, M., I. I. Ozturk, C. N. Banti, M. Manoli, E. Moushi, A. J. Tasiopoulos, A. M. Grześkiewicz, M. Kubicki i S. K. Hadjikakou. "Bismuth(III) bromide-thioamide complexes: synthesis, characterization and cytotoxic properties". Main Group Metal Chemistry 41, nr 5-6 (27.11.2018): 143–54. http://dx.doi.org/10.1515/mgmc-2018-0035.
Pełny tekst źródłaRozprawy doktorskie na temat "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.
Pełny tekst źródłaMukherjee, Suvodip. "Methodological approach on carbon-hetero bond formation reaction". Thesis, University of North Bengal, 2022. http://ir.nbu.ac.in/handle/123456789/4792.
Pełny tekst źródłaKienz, Torben [Verfasser]. "Exploration of N-ferrocenyl substituted thioamides : synthesis, properties and reactivity / Torben Kienz". Mainz : Universitätsbibliothek Mainz, 2016. http://d-nb.info/1120619912/34.
Pełny tekst źródłaEllwood, 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/.
Pełny tekst źródłaLELONG, BRUNO. "Synthese diastereoselective de thioamides ' et -dihydroxyles : une voie d'acces aux valerolactones". Caen, 1997. http://www.theses.fr/1997CAEN2059.
Pełny tekst źródłaABOUSAID, LEKBIR. "Etude cinetique de la thioamidation en serie aromatique. Synthese et caracterisation des (co)polyamide-thioamides". Caen, 1996. http://www.theses.fr/1996CAEN2031.
Pełny tekst źródłaRodriguez-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.
Pełny tekst źródłaKulesza, 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.
Pełny tekst źródłaThe 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.
Pełny tekst źródłaPerfluoroketene 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.
Pełny tekst źródłaKsiążki na temat "Synthesis of thioamide"
Reilly, William Leo 1926. Some Reactions of Fluorocarbon Nitriles: Syntheses of Amidines, Thioamides and Triazines. Creative Media Partners, LLC, 2021.
Znajdź pełny tekst źródłaCzęści książek na temat "Synthesis of thioamide"
Murai, Toshiaki. "Synthesis of Thioamides". W Chemistry of Thioamides, 45–73. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7828-7_3.
Pełny tekst źródłaKumagai, Naoya, i Masakatsu Shibasaki. "Asymmetric Synthesis Using Thioamides". W Chemistry of Thioamides, 103–25. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7828-7_5.
Pełny tekst źródłaYan, Hong, i Hai-Chao Xu. "Synthesis of Heterocycles from Thioamides". W Chemistry of Thioamides, 127–55. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7828-7_6.
Pełny tekst źródłaZhang, Xue, Jinhua Yang i Junfeng Zhao. "Ynamide-Mediated Synthetic Approach to Thioamide-Substituted Peptides". W Methods in Molecular Biology, 69–80. New York, NY: Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2489-0_6.
Pełny tekst źródłaKantlehner, W. "Synthesis from α-Phosphoryl Thioamide Derivatives". W Three Carbon-Heteroatom Bonds: Ketenes and Derivatives, 1. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00418.
Pełny tekst źródłaChou, Jonathan Chiu-Chun, Veronica E. Stafford, Grace E. Kenney i Laura M. K. Dassama. "The enzymology of oxazolone and thioamide synthesis in methanobactin". W Synthetic and Enzymatic Modifications of the Peptide Backbone, 341–73. Elsevier, 2021. http://dx.doi.org/10.1016/bs.mie.2021.04.008.
Pełny tekst źródłaTaber, Douglass F. "Enantioselective Preparation of Alkylated Stereogenic Centers". W Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0042.
Pełny tekst źródłaTaber, Douglass F. "Stereocontrolled C-N Ring Construction: The Pyne Synthesis of Hyacinthacine B 3". W Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0054.
Pełny tekst źródłaTang, R. Y. "22.1.7.2 Thioamides (Update 2024)". W Knowledge Updates 2024/1. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-122-00021.
Pełny tekst źródłaBraverman, S., M. Cherkinsky i M. L. Birsa. "Synthesis of Thioamides". W Four Carbon-Heteroatom Bonds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00203.
Pełny tekst źródłaStreszczenia konferencji na temat "Synthesis of thioamide"
Stojković, Danijela, Maja Đukić, Marija Ristić, Marina Ćendić Serafinović, Svetlana Belošević, Emina Mrkalić i Ivan Jakovljević. "Synthesis, characterization and HSA interactions of a new piano-stool ruthenium(II) complex containing a thioamide-type ligand". W 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.507s.
Pełny tekst źródłaDekamin, Mohammad G., Niaz Kheirabi i 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". W The 19th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2015. http://dx.doi.org/10.3390/ecsoc-19-a028.
Pełny tekst źródłaDotsenko, Victor, Konstantin Frolov i Sergey Krivokolysko. "DMSO-HCl System as an Efficient Oxidant of Thioamides and Selenoamides". W The 16th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2012. http://dx.doi.org/10.3390/ecsoc-16-01073.
Pełny tekst źródłaLevchenko, Arina G., Polina G. Dahno i Victor V. Dotsenko. "Synthesis of N-(hydroxymethylene)thioamides by N-hydroxymethylation of 2-cyanothioacrylamides". W ECSOC-25. Basel Switzerland: MDPI, 2021. http://dx.doi.org/10.3390/ecsoc-25-11799.
Pełny tekst źródłaHeimgartner, Heinz, Jürg Lehmann i Anthony Linden. "Site-Selective Incorporation of Thioamide-Linkages into a Growing Peptide via Variation of the 'Azirine/Oxazolone Method'". W The 1st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02033.
Pełny tekst źródłaMuntyan, Victoria S., Mariia E. Vladimirova, Alexey M. Afonin, Alexey N. Muntyan i Marina L. Roumiantseva. "ANALYSIS OF SALT-SENSITIVE AND SALT-TOLERANT SINORHIZOBIUM MELILOTI STRAINS USING DNA MICROARRAY, PHENOTYPE MICROARRAY AND GENOME MINING TECHNIQUES". W 23rd SGEM International Multidisciplinary Scientific GeoConference 2023. STEF92 Technology, 2023. http://dx.doi.org/10.5593/sgem2023/6.1/s25.15.
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