Academic literature on the topic 'Carbamyl derivatives'

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Journal articles on the topic "Carbamyl derivatives"

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Sinaga, Cinthia Uly Hotnami, and Asep Wahyu Nugraha. "Determining the Most Stable Structure of Benzamided Derivatives Using Density Functional Theory (DFT)." Indonesian Journal of Chemical Science and Technology (IJCST) 4, no. 2 (2021): 49. http://dx.doi.org/10.24114/ijcst.v4i2.27594.

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This study aims to determine the energy change ∆E and determine the most stable compound based on computation results using the Density Functional Theory (DFT) method. In determining the energy change ∆E and determining the most stable compound, computational chemical calculations were used using NWChem version 6.6 software with the DFT method with the B3LYP / 3-21G base set hybrid function, the results of the calculations were visualized using the Jmol software. The results of computational calculations on the compound Benzamide is 57467.3632844735 kJ / mol, (4 - chlorocarbonyl - benzial) - p
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Zincircioğlu, S. Burhanedtin, Naime Canoruç, Şemsettin Osmanoğlu, M. Halim Başkan, I. Yeşim Dicle та Murat Aydın. "Electron Paramagnetic Resonance of Some γ-Irradiated Amino Acid Derivatives". Zeitschrift für Naturforschung A 61, № 10-11 (2006): 577–82. http://dx.doi.org/10.1515/zna-2006-10-1110.

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γ -Irradiated powders of N-acetyl-L-arginine, Nα -carbamyl-L-arginine, N-glycyl-L-leucine and glycyl-L-alanine were investigated at room temperature by electron paramagnetic resonance. The observed species in N-acetyl-L-arginine and Nα -carbamyl-L-arginine were attributed to the CH2CHNHCNHNH2 radical, and those in N-glycyl-L-leucine and glycyl-L-alanine powders to (CH3)2CCH2 and CH3CHCOOH radicals.
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Bry, Lynn, Philip C. Chen, and David B. Sacks. "Effects of Hemoglobin Variants and Chemically Modified Derivatives on Assays for Glycohemoglobin." Clinical Chemistry 47, no. 2 (2001): 153–63. http://dx.doi.org/10.1093/clinchem/47.2.153.

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Abstract Background: Glycohemoglobin (gHb), measured as hemoglobin (Hb) A1c or as total gHb, provides a common means for assessing long-term glycemic control in individuals with diabetes mellitus. Genetic variants and chemically modified derivatives of Hb can profoundly affect the accuracy of these measurements, although effects vary considerably among commercially available methods. The prevalence of genetic variants such as HbS, HbC, and HbE, and chemically modified derivatives such as carbamyl-Hb among patient populations undergoing testing is not insignificant. Clinical laboratories and si
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Polovic, Natalija, Tanja Cirkovic-Velickovic, Marija Gavrovic-Jankulovic, et al. "IgG binding of mugwort pollen allergens and allergoids exposed to simulated gastrointestinal conditions measured by a self-developed ELISAtest." Journal of the Serbian Chemical Society 69, no. 7 (2004): 533–40. http://dx.doi.org/10.2298/jsc0407533p.

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This study considers the influence of exposure to simulated gastrointestinal conditions (saliva, gut, intestine and acidic conditions of the gut) on IgG binding of unmodified allergens and three types of LMW allergoids of Artemisia vulgaris pollen extract obtained by means of potassium cyanate succinic and maleic anhydride. It also concerns the optimization of a self-developed ELISA assay for comparison of the specific IgG binding of mugwort pollen extract and modified mugwort pollen derivatives. The ELISA was conducted with a mugwort pollen extract coupled to the plate, using the sera from 12
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Mateva, R., P. Petrov, S. Rousseva, R. Dimitrov, and G. Zolova. "On the structure of poly--caprolactams, obtained with bifunctional N-carbamyl derivatives of lactams." European Polymer Journal 36, no. 4 (2000): 813–21. http://dx.doi.org/10.1016/s0014-3057(99)00132-9.

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Callier, Anne-Claude, Beatrice Quiclet-Sire, and Samir Z. Zard. "Amidyl and carbamyl radicals by stannane mediated cleavage of O-benzoyl hydroxamic acid derivatives." Tetrahedron Letters 35, no. 33 (1994): 6109–12. http://dx.doi.org/10.1016/0040-4039(94)88089-1.

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Mateva, R., та P. Petrov. "On the activating anionic polymerization of ε-caprolactam in bulk caused by bis carbamyl derivatives". European Polymer Journal 35, № 2 (1999): 325–33. http://dx.doi.org/10.1016/s0014-3057(98)00113-x.

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Boivin, Jean, Anne-Claude Callier-Dublanchet, Béatrice Quiclet-Sire, Anne-Marie Schiano, and Samir Z. Zard. "Iminyl, amidyl, and carbamyl radicals from O-benzoyl oximes and O-benzoyl hydroxamic acid derivatives." Tetrahedron 51, no. 23 (1995): 6517–28. http://dx.doi.org/10.1016/0040-4020(95)00319-4.

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Shiba, Toshikazu, Kohji Takeda, Misako Yajima та Makoto Tadano. "Genes from Pseudomonas sp. Strain BS Involved in the Conversion of l-2-Amino-Δ2-Thiazolin-4-Carbonic Acid to l-Cysteine". Applied and Environmental Microbiology 68, № 5 (2002): 2179–87. http://dx.doi.org/10.1128/aem.68.5.2179-2187.2002.

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ABSTRACT dl-2-amino-Δ2-thiazolin-4-carbonic acid (dl-ATC) is a substrate for cysteine synthesis in some bacteria, and this bioconversion has been utilized for cysteine production in industry. We cloned a DNA fragment containing the genes involved in the conversion of l-ATC to l-cysteine from Pseudomonas sp. strain BS. The introduction of this DNA fragment into Escherichia coli cells enabled them to convert l-ATC to cysteine via N-carbamyl-l-cysteine (l-NCC) as an intermediate. The smallest recombinant plasmid, designated pTK10, contained a 2.6-kb insert DNA fragment that has l-cysteine synthet
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Zieve, Leslie, Carolyn Lyftogt, and Donna Raphael. "Ammonia toxicity: Comparative protective effect of various arginine and ornithine derivatives, aspartate, benzoate, and carbamyl glutamate." Metabolic Brain Disease 1, no. 1 (1986): 25–35. http://dx.doi.org/10.1007/bf00998474.

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Dissertations / Theses on the topic "Carbamyl derivatives"

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Wang, Haiyu, та Abbas Shilabin. "Synthesis of 2-Carbamoyl-4-Oxo-1,5-Diazabicyclo [3.2.1] Octane Derivatives as a Possible Inhibitors of Serine β-Lactamases". Digital Commons @ East Tennessee State University, 2018. https://dc.etsu.edu/asrf/2018/schedule/178.

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Antibiotic resistance is becoming ever more severe due in part to the increasing use of antibiotic drugs. One significant contributor to this problem is the production of β-lactamase enzymes that provide resistance to common β-lactam antibiotics. The scope of this research is to synthesize and study the β-lactamase inhibitors of 2-carbamoyl-4-oxo-1,5-diazabicyclo [3.2.1] octane derivatives. Currently the research process is in the beginning stages of synthesizing three compounds: (R)-hexahydro-6-oxopyrimidine-4-carboxylic acid (1a), hexahydro-2,2-dimethyl-6-oxopyrimidine-4-carboxylic acid (1b)
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Li, Junming. "The performance characterization of carbazole/dibenzothiophene derivatives in modern OLEDs." Doctoral thesis, Humboldt-Universität zu Berlin, Mathematisch-Naturwissenschaftliche Fakultät, 2017. http://dx.doi.org/10.18452/17678.

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Ein vielversprechendes Design für organische lichtemittierende Dioden (OLEDs) verwendet eine Wirt-Gast-Strategie durch Dispergieren einer kleinen Menge eines hocheffizienten Emitters (der Gast) in eine passende Transportmatrix (der Wirt). Die Aufgabe des Wirts ist den Exzitonentranport zum Emitter sicherzustellen und den Zerfall von Triplet-Exzitonen zu verhindern, und damit eine hohe Bauteilperformance zu erreichen. Die vorliegende Arbeit konzentriert sich auf die Beziehung zwischen Molekülstruktur und optoelektrischer Eigenschaften von Carbazol/Dibenzothiophen-Derivaten. Die Untersuchung um
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Tu, Tzu-Chiang, and 杜自強. "Study of synthesis of 4-carbamoyl-1-(5-carboxypentyl)pyridin-1-ium salts and derivatives." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/41311024910203387926.

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碩士<br>國立高雄師範大學<br>化學系<br>100<br>A series of 4-carbamoyl-1-(5-carboxypentyl)pyridin-1-ium salts with different anions (Br、NO3、BF4、PF6、OTf、BPh4、ZnBr42-、CuBr42-)and deprotonated carboxylate zwitterion have been synthesized and anions (Br、PF6、OTf) have been characterized by single crystal X-ray diffraction. The results demonstrate that the unparallel diamide-substituted pyridinium salts form a dimerized rectangular building block and a 2-D rectangular structure via N-H∙∙∙O and C-H∙∙∙O hydrogen bonding (OTf-), a 2-D sheet structure (Br-, PF6-) via N-H∙∙∙O hydrogen bonding catemers, and a 2-D plate
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Chan, Chien-Ching, and 詹前慶. "Substituent and Solvent Effects on Keto-Enol Tautomerism of Acetyl, Carbamoyl Derivatives, and Their Radical Cations." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/41560203078684144988.

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碩士<br>國立清華大學<br>化學系<br>87<br>Abstract The results of DFT study of the substituent effects on molecular structures, relative stabilities, and mechanisms of intramolecular proton transfer in isolated acetyl and carbamoyl drivatives, for both neutral molecules and their radical cations, are reported. The reaction in the presence of one and two water molecules is also investigated. Furthermore, the effect of bulk water is considered for the system with two water molecules using the PCM continuum models. All of geometries of the local minima and transition states were optimized without
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WU, DENG-LU, and 吳登陸. "Synthesis of Conjugated Copolymers Based on 1,3-Bis(carbazol-9-yl)Benzene and Thiophene Derivatives for Electrochromic Device." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/tca8hw.

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碩士<br>國立高雄應用科技大學<br>化學工程與材料工程系博碩士班<br>104<br>In this study, 1,3-bis(carbazol-9-yl)benzene (BiCP) and three 3,4-ethylenedioxythiophene derivatives (3,4-ethylenedioxythiophene (EDOT), 2,2-dimethyl-3,4-propylenedioxythiophene (ProDOT-Me2), and 3,4-ethylenedithiathiophene (EDTT)) are copolymerized electrochemically on indium tin oxide (ITO) to obtain P(BiCP-co-EDOT), P(BiCP-co-ProDOT-Me2), and P(BiCP-co-EDTT), respectively. Spectroelectrochemical properties of polymer films reveal that P(BiCP-co-ProDOT-Me2) film is yellowish in the reduced state, yellow in the intermediate state, and dark green in
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Wu, Li-Chu, and 吳禮竹. "Fluorescent and Electrochromic Polymers from 2,8-Di(carbazol-9-yl)dibenzothiophene and Its S,S-Dioxide Derivative." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/s57896.

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碩士<br>國立臺北科技大學<br>化學工程研究所<br>101<br>This thesis deals with the synthesis and characterization of two carbazole-endcapped monomers, named as 2,8-di(carbazol-9-yl)dibenzothiophene (SCz) and 2,8-di(carbazol-9-yl)dibenzothiophene S,S-dioxide (SO2Cz), and their derived polymers PSCz and PSO2Cz prepared by both chemically oxidative coupling polymerization in the presence of FeCl3 and electrochemically oxidative process. Two referenced compounds with tert-butyl blocking groups on their carbazole units, namely 2,8-di(3,6-di-tert-butylcarbazol-9-yl)dibenzothiophene (StBCz) and 2,8-di(3,6-di-tert- butyl
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Hsueh, Ju-Chun, and 薛如君. "Preparation and Optoelectronic Properties of Electropolymerized Polymeric Films from Di(carbazol-9-yl)-substituted Triphenylamine and N-Phenylcarbazole Derivatives." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/tu49b9.

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碩士<br>國立臺北科技大學<br>化學工程研究所<br>101<br>Two carbazole end-capped monomers containing triphenylamine or N-phenylcarbazole as an interior core, namely 4,4’-di(carbazol-9-yl)- 4”-methoxytriphenylamine (TPA-2Cz) and 3,6-di(carbazol-9-yl)-N-(4-methoxy- phenyl)carbazole (PhCz-2Cz), were prepared by a well-known chemistry from readily available reagents. The electrochemistry and electropolymerization of these two monomers were investigated and compared with those of structurally similar analogues with tert-butyl groups attaching on the active sites of the end-capped carbazole units. The polymeric films
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Book chapters on the topic "Carbamyl derivatives"

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Marinaki, Anthony M., Lynette D. Fairbanks, and Richard W. E. Watts. "Disorders of purine and pyrimidine metabolism." In Oxford Textbook of Medicine, edited by Timothy M. Cox. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198746690.003.0230.

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Disorders of purine and pyrimidine metabolism are due to abnormalities in the biosynthesis, interconversion, and degradation of the purines—adenine and guanine—and of the pyrimidines—cytosine, thymine, and uracil. The purine nucleotides, their cyclic derivatives (cAMP and cGMP), and their more highly phosphorylated derivatives have functions in many aspects of intermediary metabolism. Purine compounds also function as signal transducers, neurotransmitters, vasodilators, and mediators of platelet aggregation. Disorders of purine metabolism—the end point of purine metabolism in humans is uric ac
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Rossi, L. "Carbamic Acids and Derivatives." In Four Carbon-Heteroatom Bonds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00579.

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Stien, D. "From Carbamoyl Halides and Related Derivatives." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00011.

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Braverman, S., M. Cherkinsky, and M. L. Birsa. "Synthesis of Carbamic Acid Derivatives." In Four Carbon-Heteroatom Bonds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00079.

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Tidwell, T. T. "Carbamoyl-Substituted Esters by Successive Amine and Alcohol Addition." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00644.

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Stien, D. "Synthesis from Carbamic Acids and Related Derivatives." In Three Carbon-Heteroatom Bonds: Esters and Lactones; Peroxy Acids and R(CO)OX Compounds; R(CO)X, X=S, Se, Te. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-021-00009.

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Murai, T. "22.2.5 Selenocarboxylic Acids and Derivatives (Update 2024)." In Knowledge Updates 2024/2. Georg Thieme Verlag KG, 2024. http://dx.doi.org/10.1055/sos-sd-122-00194.

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Abstract Selenocarboxylic acids and their derivatives are the selenium isologues of carboxylic, thioic, carbamic, and carbonic acids, and the corresponding esters, amides, and ureas, and are distinguished by the presence of a C=Se bond. The synthesis of these selenium analogues primarily involves incorporating selenium atoms into precursor molecules. This can be achieved by reducing elemental selenium to produce Se2– species, which are then introduced into electrophilic species. Alternatively, carbon nucleophiles can directly bond with elemental selenium, forming carbon–selenium bonds. Compoun
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Tidwell, T. T. "A Cyclic Carbamoyl Ester by Addition of an Amino Alcohol to a 1,2-Bisketene." In Three Carbon-Heteroatom Bonds: Thio-, Seleno-, and Tellurocarboxylic Acids and Derivatives; Imidic Acids and Derivatives; Ortho Acid Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-023-00645.

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Boyd, G. V. "From α-Hydroxy Ketones and Carbamic Acid Derivatives." In Five-Membered Hetarenes with One Chalcogen and One Additional Heteroatom. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-011-00565.

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Senet, J. P. G. "By Chlorination of N,N-Disubstituted Carbamic Acid Derivatives." In Four Carbon-Heteroatom Bonds. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00386.

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