Academic literature on the topic 'Organic dithiocarbamate'

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Journal articles on the topic "Organic dithiocarbamate"

1

Pedras, M. Soledade, and Francis I. Okanga. "Metabolism of analogs of the phytoalexin brassinin by plant pathogenic fungi." Canadian Journal of Chemistry 78, no. 3 (2000): 338–46. http://dx.doi.org/10.1139/v00-024.

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he metabolism of analogs of the cruciferous phytoalexin brassinin by the phytopathogenic fungi Phoma lingam (Tode ex Fr.) "virulent" and "avirulent" groups (sexual stage Leptosphaeria maculans (Desm.) Ces. et de Not.) and Alternaria brassicae (Berk.) Sacc. is reported. It was established that each pathogen detoxified methyl tryptamine dithiocarbamate, although yielding different metabolic products. While the biotransformation by virulent P. lingam proceeded to yield methyl 3a-hydroxy-3,3a,8,8a-tetrahydropyrrolo[2,3-b]indol-1(2H)-yl carbodithioate and indole-3-acetic acid as final products, avi
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2

Ziyaei Halimehjani, Azim, Petr Beier та Maryam Khalili Foumeshi. "Synthesis of Novel α,β-Unsaturated Sulfonic Acid Derivatives Containing Dithiocarbamate/Xanthate Groups by Ring Opening of an α,β-Unsaturated γ-Sultone". Synlett 31, № 10 (2020): 987–90. http://dx.doi.org/10.1055/s-0040-1707970.

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An efficient method is disclosed for the synthesis of novel α,β-unsaturated sulfonic acid derivatives containing dithiocarbamate/xanthate groups through ring opening of an α,β-unsaturated γ-sultone with dithiocarbamic acid salts or xanthates prepared in situ. Treatment of the primary products with hydrochloric acid afforded the corresponding β-chloro-γ-(dithiocarbamato)propanesulfonic acids in excellent yields.
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3

Oliveira, Johny Wysllas de Freitas, Hugo Alexandre Oliveira Rocha, Wendy Marina Toscano Queiroz de Medeiros, and Marcelo Sousa Silva. "Application of Dithiocarbamates as Potential New Antitrypanosomatids-Drugs: Approach Chemistry, Functional and Biological." Molecules 24, no. 15 (2019): 2806. http://dx.doi.org/10.3390/molecules24152806.

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Dithiocarbamates represent a class of compounds that were evaluated in different biomedical applications because of their chemical versatility. For this reason, several pharmacological activities have already been attributed to these compounds, such as antiparasitic, antiviral, antifungal activities, among others. Therefore, compounds that are based on dithiocarbamates have been evaluated in different in vivo and in vitro models as potential new antimicrobials. Thus, the purpose of this review is to present the possibilities of using dithiocarbamate compounds as potential new antitrypanosomati
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4

Humeres, Eduardo, Byung Sun Lee, and Nito Angelo Debacher. "Mechanisms of Acid Decomposition of Dithiocarbamates. 5. Piperidyl Dithiocarbamate and Analogues." Journal of Organic Chemistry 73, no. 18 (2008): 7189–96. http://dx.doi.org/10.1021/jo801015t.

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5

Odularu, Ayodele T., and Peter A. Ajibade. "Dithiocarbamates: Challenges, Control, and Approaches to Excellent Yield, Characterization, and Their Biological Applications." Bioinorganic Chemistry and Applications 2019 (February 6, 2019): 1–15. http://dx.doi.org/10.1155/2019/8260496.

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Progresses made in previous researches on syntheses of dithiocarbamates led to increase in further researches. This paper reviews concisely the challenges experienced during the synthesis of dithiocarbamate and mechanisms to overcome them in order to obtain accurate results. Aspects of its precursor’s uses to synthesize adducts, nanoparticles, and nanocomposites are reported. Some common characterization techniques used for the synthesized products were assessed. Biological applications are also reported.
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6

Das, Rituparna, Balaram Mukhopadhyay, and Bedangshu Mishra. "A ‘Turn-on’ Fluorescence Glycosyl Dithiocarbamate Probe for Selective Fluoride Sensing in Aqueous Medium." Synlett 29, no. 15 (2018): 2001–5. http://dx.doi.org/10.1055/s-0037-1610533.

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A glycosyl dithiocarbamate derivative is developed as a ‘turn on’ fluorescent sensor for fluorides in aqueous medium. The probe is prepared through a simple chemical strategy reported earlier from our group. The virtually nonfluorescent probe showed significant enhancement of fluorescence upon interaction with fluorides in aqueous solution. It was seen to be selective to fluorides too as the interactions with various other anions resulted in very low increase in fluorescence. The simple preparation and unique interaction of the dithiocarbamato derivative with fluorides in aqueous solution prom
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7

Adeyemi, Jerry O., and Damian C. Onwudiwe. "Chemistry and Some Biological Potential of Bismuth and Antimony Dithiocarbamate Complexes." Molecules 25, no. 2 (2020): 305. http://dx.doi.org/10.3390/molecules25020305.

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Interest in the synthesis of Bi(III) and Sb(III) dithiocarbamate complexes is on the rise, and this has been attributed to their wide structural diversity and their interesting application as biological agents and in solid state/materials chemistry. The readily available binding sites of the two sulphur atoms within the dithiocarbamate moiety in the complexes confers a wide variety of geometry and interactions that often leads to supramolecular assemblies. Although none of the bismuth or antimony metals are known to play any natural biological function, their dithiocarbamate complexes, however
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8

Ziyaei-Halimjani, Azim, та Mohammad R. Saidi. "Synthesis of β-hydroxy dithiocarbamate derivatives via regioselective addition of dithiocarbamate anion to epoxide in water". Canadian Journal of Chemistry 84, № 11 (2006): 1515–19. http://dx.doi.org/10.1139/v06-150.

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The reactions of different dithiocarbamate anions with epoxides were investigated in water. With this method, β-hydroxy dithiocarbamate derivatives were synthesized in high yields. The reaction was also carried out in DMF in the presence of lithium perchlorate with a simple work-up procedure, and the results are compared.Key words: hydroxy dithiocarbamate, dithiocarbamate anion, epoxide, water.
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9

Drake, John E., Layla N. Khasrou, Anil G. Mislankar, and Raju Ratnani. "Dimethyltellurium(IV) derivatives with mixed 1,1-dithio ligands. Crystal structures of Me2Te[S2CNMe2][S2COEt] and Me2Te[S2CNEt2][S2COMe]." Canadian Journal of Chemistry 77, no. 7 (1999): 1262–73. http://dx.doi.org/10.1139/v99-123.

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Mixed ligand derivatives of Me2TeLL'2, where L = N,N-dialkyl dithiocarbamate or O,O-alkylene dithiophosphate and L' = O-alkyl dithiocarbonate, have been synthesized and characterized by elemental analysis, 1H, 13C, 31P, and 125Te NMR spectroscopy and infrared and Raman spectroscopy, and X-ray crystallography. Me2Te[S2CNMe2][S2COEt], 8: P[Formula: see text] (no. 2), with cell parameters a = 10.073(3) Å, b = 10.139(2) Å, c = 9.108(2) Å, α = 92.36(2)°, β = 115.55(2)°, γ = 111.19(2)°, V = 760.7(4) Å3, Z = 2, R = 0.0343, Rw = 0.0296. Me2Te[S2CNEt2][S2COMe], 9: P21/c (no. 14) with cell parameters a
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10

Wieber, Markus, and Stefan Rohse. "TRIMETHYLTELLURONIUMXANTHOGENATE, -THIOXANTHOGENATE UND -DITHIOCARBAMATE." Phosphorus, Sulfur, and Silicon and the Related Elements 55, no. 1 (1991): 79–83. http://dx.doi.org/10.1080/10426509108045925.

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