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Journal articles on the topic 'Organic dithiocarbamate'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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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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11

Abbaszadeh, Abolfazl, and Azadeh Tadjarodi. "Speciation analysis of inorganic arsenic in food and water samples by electrothermal atomic absorption spectrometry after magnetic solid phase extraction by a novel MOF-199/modified magnetite nanoparticle composite." RSC Advances 6, no. 114 (2016): 113727–36. http://dx.doi.org/10.1039/c6ra21819a.

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12

Sun, Nan, Bin Li, Jianping Shao, et al. "A general and facile one-pot process of isothiocyanates from amines under aqueous conditions." Beilstein Journal of Organic Chemistry 8 (January 10, 2012): 61–70. http://dx.doi.org/10.3762/bjoc.8.6.

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A general and facile one-pot protocol for the preparation of a broad range of alkyl and aryl isothiocyanates has been developed from their corresponding primary amines under aqueous conditions. This synthetic process involves an in situ generation of a dithiocarbamate salt from the amine substrate by reacting with CS2 followed by elimination to form the isothiocyanate product with cyanuric acid as the desulfurylation reagent. The choice of solvent is of decisive importance for the successful formation of the dithiocarbamate salt particularly for highly electron-deficient substrates. This novel

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13

Dutta, Soumya, Manas Mondal, Tubai Ghosh, and Amit Saha. "Unprecedented thiocarbamidation of nitroarenes: a facile one-pot route to unsymmetrical thioureas." Organic Chemistry Frontiers 6, no. 1 (2019): 70–74. http://dx.doi.org/10.1039/c8qo00752g.

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14

Sugimoto, Hirohiko, Itsuo Makino, and Kentaro Hirai. "Activation of dithiocarbamate by 2-halothiazolium salts." Journal of Organic Chemistry 53, no. 10 (1988): 2263–67. http://dx.doi.org/10.1021/jo00245a025.

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15

Aly, Ashraf A., Alan B. Brown, Tarek M. I. Bedair, and Esam A. Ishak. "Dithiocarbamate salts: biological activity, preparation, and utility in organic synthesis." Journal of Sulfur Chemistry 33, no. 5 (2012): 605–17. http://dx.doi.org/10.1080/17415993.2012.718349.

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16

Baba, Ibrahim, Amirah Faizah Abdul Muthalib, Yang Farina Abdul Aziz, and Ng Seik Weng. "New Dithiocarbamate Compounds from Organotin(IV)." Phosphorus, Sulfur, and Silicon and the Related Elements 186, no. 6 (2011): 1326–29. http://dx.doi.org/10.1080/10426507.2010.548841.

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17

Vasiliev, A., and A. Polackov. "Synthesis of Potassium (1,1-Dioxothiolan-3-yl)-dithiocarbamate." Molecules 5, no. 12 (2000): 1014–17. http://dx.doi.org/10.3390/50801014.

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18

Zhang, Dingjun, Jianmin Chen, Yongming Liang, and Huidi Zhou. "Facile Synthesis of Novel Ionic Liquids Containing Dithiocarbamate." Synthetic Communications 35, no. 4 (2005): 521–26. http://dx.doi.org/10.1081/scc-200049773.

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19

Liu, Aili, Xinnan Mao, Zhoumin Xiao, et al. "One-pot synthesis of dumbbell shaped PbS–Te hybrids with promising photothermal properties." Canadian Journal of Chemistry 98, no. 12 (2020): 799–805. http://dx.doi.org/10.1139/cjc-2020-0007.

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The development of multi-component photothermal agents has attracted increasing attention due to their potential applications in energy conversion, medical treatments, etc. Herein, a dumbbell shaped PbS–Te heterostructure was prepared via a one-pot microwave-assisted decomposition of lead dimethyl dithiocarbamate and tellurium diethyl dithiocarbamate. The as-obtained PbS–Te hybrids exhibit excellent photothermal stability and strong optical absorption over a broad wavelength range spanning from ultraviolet to near-infrared, where the photothermal conversion efficiency could reach as high as 12

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20

Kociok-Köhn, Gabriele, Kieran C. Molloy, and Anna L. Sudlow. "Molecular routes to Cu2ZnSnS4: A comparison of approaches to bulk and thin-film materials." Canadian Journal of Chemistry 92, no. 6 (2014): 514–24. http://dx.doi.org/10.1139/cjc-2013-0497.

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A range of xanthates (R′3P)2CuS2COR [R′ = Ph, R = Et (1), i-Pr (2), t-Bu (3), t-Amyl (4); R′ = PhO, R = Et (5), R′ = n-Bu, R = Et (6), Bun (7)], M(S2COR)2 [M = Sn R = Et (8); Zn, R = Et (10), i-Pr (11), n-Pr (12), n-Bu (13), n-Hex (14)], Sn(S2COEt)4 (9), Zn(S2COEt)2.TMEDA (15) have been synthesised and their thermal decomposition profiles delineated by TGA. A parallel range of dithiocarbamates (R′3P)2CuS2CN(Me)R [R′ = Ph, R = Bun (16), Bz (17)], M[S2CN(Me)R]2 [M = Sn, R = Bun (18), Bz (19); M = Zn, R = Bun (21), Bz (22)] has been similarly assessed. Although precursor combinations have been fo

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21

Khoshdoun, Maryam, Salman Taheri, Parandis Daneshgar, Hamid R. Jamshidi, and Azim Ziyaei Halimehjani. "Synthesis of 5‐amino‐1,3,4‐thiadiazoles containing dithiocarbamate groups." Journal of Heterocyclic Chemistry 57, no. 3 (2020): 1063–70. http://dx.doi.org/10.1002/jhet.3841.

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22

Li, Bowen, Shuo Zhou, Shucheng Wang, Xingyi Sun, Zemei Ge, and Runtao Li. "Efficient synthesis of organic sulfonic acid derivatives containing dithiocarbamate side chains." Tetrahedron 72, no. 27-28 (2016): 3885–89. http://dx.doi.org/10.1016/j.tet.2016.05.011.

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23

Zhang, Jingjing, Nicholas R. Myllenbeck, and Trisha L. Andrew. "Synthesis and Properties of Dithiocarbamate-Linked Acenes." Organic Letters 19, no. 1 (2016): 210–13. http://dx.doi.org/10.1021/acs.orglett.6b03492.

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24

Aly, Ashraf A., Alan B. Brown, Tarek M. I. Bedair, and Esam A. Ishak. "ChemInform Abstract: Dithiocarbamate Salts: Biological Activity, Preparation, and Utility in Organic Synthesis." ChemInform 44, no. 9 (2013): no. http://dx.doi.org/10.1002/chin.201309224.

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25

Toscani, Anita, Eeva K. Heliövaara, Jubeda B. Hena, Andrew J. P. White, and James D. E. T. Wilton-Ely. "Multimetallic Alkenyl Complexes Bearing Macrocyclic Dithiocarbamate Ligands." Organometallics 34, no. 2 (2015): 494–505. http://dx.doi.org/10.1021/om5011269.

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26

Ajibade, Peter A., Fartisincha P. Andrew, Nandipha L. Botha, and Nolwazi Solomane. "Synthesis, Crystal Structures and Anticancer Studies of Morpholinyldithiocarbamato Cu(II) and Zn(II) Complexes." Molecules 25, no. 16 (2020): 3584. http://dx.doi.org/10.3390/molecules25163584.

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Cu(II) and Zn(II) morpholinyldithiocarbamato complexes, formulated as [Cu(MphDTC)2] and [Zn(μ-MphDTC)2(MphDTC)2], where MphDTC is morpholinyldithiocarbamate were synthesized and characterized by elemental analysis, spectroscopic techniques and single-crystal X-ray crystallography. The molecular structure of the Cu(II) complex revealed a mononuclear compound in which the Cu(II) ion was bonded to two morpholinyl dithiocarbamate ligands to form a four-coordinate distorted square planar geometry. The molecular structure of the Zn(II) complex was revealed to be dinuclear, and each metal ion was bon

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27

Bergerbit, Cédric, Bárbara Farías-Mancilla, Lucie Seiler, et al. "Synthesis of PMMA-based block copolymers by consecutive irreversible and reversible addition–fragmentation chain transfer polymerizations." Polymer Chemistry 10, no. 48 (2019): 6630–40. http://dx.doi.org/10.1039/c9py01181a.

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Xanthate and dithiocarbamate functionalized PMMAs obtained by free radical polymerization in the presence of xanthogen and dithiuram disulfide were used for chain extension with less activated monomers such as vinyl acetate and ethylene.

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28

Eschliman, Kayla, and Stefan Bossmann. "Synthesis of Isothiocyanates: An Update." Synthesis 51, no. 08 (2019): 1746–52. http://dx.doi.org/10.1055/s-0037-1612303.

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Isothiocyanates (ICTs) are a group of molecules that can be used for many different purposes, they exhibit anticancer, antimicrobial, antibiotic, and anti-inflammatory properties. The synthesis of isothiocyanates has been a focus of many researchers for nearly the past 100 years. One of the most common synthetic methods is to form a dithiocarbamate salt, either as the first step or in situ, and then treat the salt with a desulfurization agent to reach the isothiocyanate. There are many different desulfurization agents available. Among these, there are eleven in particular that will be discusse

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29

Borràs, Jordi, Julie Foster, Roxana Kashani, et al. "New Bioconjugated Technetium and Rhenium Folates Synthesized by Transmetallation Reaction with Zinc Derivatives." Molecules 26, no. 8 (2021): 2373. http://dx.doi.org/10.3390/molecules26082373.

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The zinc dithiocarbamates functionalized with folic acid 2Zn and 3Zn were synthesized with a simple straightforward method, using an appropriated folic acid derivative and a functionalized zinc dithiocarbamate (1Zn). Zinc complexes 2Zn and 3Zn show very low solubilities in water, making them useful for preparing Tc-99m radiopharmaceuticals with a potentially high molar activity. Thus, the transmetallation reaction in water medium between the zinc complexes 2Zn or 3Zn and the cation fac-[99mTc(H2O)3(CO)3]+, in the presence of the monodentate ligand TPPTS, leads to the formation of the 2 + 1 com

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30

Todorovic, Zoran, Predrag Polic, Tibor Sabo, and Milorad Cakic. "Preconcentration method for trace metals in natural waters using 4-morpholine dithiocarbamate." Journal of the Serbian Chemical Society 67, no. 12 (2002): 879–85. http://dx.doi.org/10.2298/jsc0212879t.

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The optimum conditions were found for the preconcentration of trace metals in natural waters and model samples with standard metals concentrations by using 4-morpholine dithiocarbamate. The formed complexes were extracted with chloroform. Different methods for recovering the metals from the organic solvent were studied and compared before AAS metal analysis. The developed preconcentration method was successfully applied to the determination of trace metals concentrations in water samples from the "Barje" lake (Leskovac, Yugoslavia).

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31

Kaplancıli, Zafer Asim, Gülhan Turan-Zitouni, Gilbert Revial, and Gökalp Işcan. "SYNTHESIS OF SOME DITHIOCARBAMATE DERIVATIVES AND THEIR ANTIMICROBIAL ACTIVITY." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 7 (2004): 1449–54. http://dx.doi.org/10.1080/10426500490463664.

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32

Dutta, Soumya, and Amit Saha. "Iodine mediated direct coupling of benzylic alcohols with dithiocarbamate anions: An easy access of S-benzyl dithiocarbamate esters under neat reaction condition." Tetrahedron Letters 61, no. 41 (2020): 152382. http://dx.doi.org/10.1016/j.tetlet.2020.152382.

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33

Adeyemi, Jerry O., and Damian C. Onwudiwe. "PbS Nanoparticles Prepared Using 1, 10-Phenanthroline Adduct of Lead(II) Bis(N-alkyl-N-phenyl dithiocarbamate) as Single Source Precursors." Molecules 25, no. 9 (2020): 2097. http://dx.doi.org/10.3390/molecules25092097.

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Dithiocarbamate complexes have remained prominent as single source precursors for the synthesis of clean metal sulfide nanoparticles. This study reports the synthesis of lead sulfide (PbS) nanoparticles using some novel complexes of 1, 10-phenanthroline lead(II) bis(N-alkyl-N-phenyl dithiocarbamate), represented as [Pb(L1)2phen] (1) and [Pb(L2)2phen] (2) (where L1 = bis(N-ethyl-N-phenyldithiocarbamate; L2 = bis(N-butyl-N-phenyldithiocarbamate); phen = 1, 10 phenanthroline) as a single source precursors. The complexes (1 and 2) were synthesized and characterized using various spectroscopic tech

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34

Nilakantan, Lakshmi, David R. McMillin, and Paul R. Sharp. "Emissive Biphenyl Cyclometalated Gold(III) Diethyl Dithiocarbamate Complexes." Organometallics 35, no. 14 (2016): 2339–47. http://dx.doi.org/10.1021/acs.organomet.6b00275.

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35

Koivukorpi, Juha, and Erkki Kolehmainen. "Synthesis of Both Ionic Species of Ammonium Dithiocarbamate Derived Cholic Acid Moieties." Molecules 16, no. 8 (2011): 6306–12. http://dx.doi.org/10.3390/molecules16086306.

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36

Baghershiroudi, Mahrokh, Kazem D. Safa, Khosro Adibkia, and Farzaneh Lotfipour. "Synthesis and antibacterial evaluation of new sulfanyltetrazole derivatives bearing piperidine dithiocarbamate moiety." Synthetic Communications 48, no. 3 (2018): 323–28. http://dx.doi.org/10.1080/00397911.2017.1401639.

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37

Ohtake, Norikazu, Hideaki Imamura, Hideki Jona, et al. "Novel dithiocarbamate carbapenems with anti-MRSA activity." Bioorganic & Medicinal Chemistry 6, no. 7 (1998): 1089–101. http://dx.doi.org/10.1016/s0968-0896(98)00069-8.

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38

Imamura, Hideaki, Norikazu Ohtake, Hideki Jona, et al. "Dicationic dithiocarbamate carbapenems with anti-MRSA activity." Bioorganic & Medicinal Chemistry 9, no. 6 (2001): 1571–78. http://dx.doi.org/10.1016/s0968-0896(01)00044-x.

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39

Fanjul-Bolado, Pablo, Ronen Fogel, Janice Limson, Cristina Purcarea, and Alina Vasilescu. "Advances in the Detection of Dithiocarbamate Fungicides: Opportunities for Biosensors." Biosensors 11, no. 1 (2020): 12. http://dx.doi.org/10.3390/bios11010012.

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Dithiocarbamate fungicides (DTFs) are widely used to control various fungal diseases in crops and ornamental plants. Maximum residual limits in the order of ppb-ppm are currently imposed by legislation to prevent toxicity problems associated with excessive use of DTFs. The specific analytical determination of DTFs is complicated by their low solubility in water and organic solvents. This review summarizes the current analytical procedures used for the analysis of DTF, including chromatography, spectroscopy, and sensor-based methods and discusses the challenges related to selectivity, sensitivi

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40

Dou, Ye-Hong, Shou-De Xu, Yi Chen, and Xiang-Hua Wu. "Synthesis, characterization, and anticancer activity of dithiocarbamate ruthenium(II) complexes." Phosphorus, Sulfur, and Silicon and the Related Elements 192, no. 11 (2017): 1219–23. http://dx.doi.org/10.1080/10426507.2017.1359594.

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41

Yu, Jia-Ying, Xue-Qiang Li, and Meng-Xue Wei. "Synthesis and biological activities of artemisinin-piperazine-dithiocarbamate derivatives." European Journal of Medicinal Chemistry 169 (May 2019): 21–28. http://dx.doi.org/10.1016/j.ejmech.2019.02.071.

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42

Ramesh, Rao, Hong, and Reddy. "Molecular Design, Synthesis, and Biological Evaluation of 2-Hydroxy-3-Chrysino Dithiocarbamate Derivatives." Molecules 24, no. 17 (2019): 3038. http://dx.doi.org/10.3390/molecules24173038.

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A series of 2-hydroxy-3-chrysino dithiocarbamate derivatives (3a–k) were designed, synthesized, and characterized for their structure determination by 1H NMR, 13C NMR, and HRMS (ESI) spectral data. They were screened for their in vitro biological activities against a panel of selected bacterial and fungal strains. These antimicrobial studies indicate that some of the analogues manifested significant activity compared to standard drugs. Among the synthetic analogues (3a–k), compounds 3d, 3f, and 3j exhibited very good antibacterial activity and compounds 3d, 3f, and 3h showed very good antifung

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43

Zhao, Chun Lin, Li Xing, Xiao Hong Liang, et al. "Photoluminescence Enhancement of CdS Nanocrystals Fabricated on Dithiocarbamate Functionalized PET Substrates." Key Engineering Materials 512-515 (June 2012): 1511–15. http://dx.doi.org/10.4028/www.scientific.net/kem.512-515.1511.

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Cadmium sulfide (CdS) nanocrystals (NCs) were self-assembled and in-situ immobilized on the dithiocarbamate (DTCs)-functionalized polyethylene glycol terephthalate (PET) substrates between the organic (carbon disulfide diffused in n-hexane) –aqueous (ethylenediamine and Cd2+ dissolved in water) interface at room temperature. Powder X-ray diffraction measurement revealed the hexagonal structure of CdS nanocrystals. Morphological studies performed by scanning electron microscopy (SEM) and high-resolution transmission electron microscope (HRTEM) showed the island-like structure of CdS nanocrystal

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44

Wang, Jianxin, Mini Thomas, Peng Lin, Ji-Xin Cheng, Daniela E. Matei, and Alexander Wei. "siRNA Delivery Using Dithiocarbamate-Anchored Oligonucleotides on Gold Nanorods." Bioconjugate Chemistry 30, no. 2 (2018): 443–53. http://dx.doi.org/10.1021/acs.bioconjchem.8b00723.

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45

Turner, S. Richard, and Richard W. Blevins. "Photoinitiated block copolymer formation using dithiocarbamate free radical chemistry." Macromolecules 23, no. 6 (1990): 1856–59. http://dx.doi.org/10.1021/ma00208a050.

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46

Gorshkov, Nikolay I., Andrey Yu Murko, Irina I. Gavrilova, et al. "Synthesis of Water-Soluble Copolymers of N-vinylpyrrolidone with N-vinyldithiocarbamate as Multidentate Polymeric Chelation Systems and Their Complexes with Indium and Gallium." Molecules 25, no. 20 (2020): 4681. http://dx.doi.org/10.3390/molecules25204681.

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Dithiocarbamate (DTC) derivatives of N-vinylpyrrolidone-N-vinylamine (VP–VA) copolymers were synthesized via reaction between the copolymers and carbon disulfide in alkaline medium; molecular masses of the products were 12 and 29 kDa; the VP:VDTC ratios were 94:6 and 83:17 mol.%. Complexation between the obtained DTC derivatives and metal ions (indium and gallium) was investigated. It was demonstrated that metal–DTC ligand complexes with 1:3 ratio between components were formed. Gallium metal–polymer complexes (MPC) were unstable in solution. Individual indium MPC were isolated and characteriz

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Patel, Alpesh, and Kibret Mequanint. "The kinetics of dithiocarbamate-mediated polyurethane-block-poly(methyl methacrylate) polymers." Polymer 50, no. 19 (2009): 4464–70. http://dx.doi.org/10.1016/j.polymer.2009.07.045.

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Asar, Farzane Jafari, Farinaz Soleymani, Seyyed Emad Hooshmand, and Azim Ziyaei Halimehjani. "Direct synthesis of piperazines containing dithiocarbamate derivatives via DABCO bond cleavage." Tetrahedron Letters 61, no. 49 (2020): 152610. http://dx.doi.org/10.1016/j.tetlet.2020.152610.

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Sharma, Jyoti, Yashpal Singh, and Audhesh Kumar Rai. "SYNTHESIS AND SPECTROSCOPIC CHARACTERIZATION OF HETEROCYCLIC DITHIOCARBAMATE COMPLEXES OF TRIORGANOTIN (IV)." Phosphorus, Sulfur, and Silicon and the Related Elements 112, no. 1-4 (1996): 19–26. http://dx.doi.org/10.1080/10426509608046344.

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Behalo, M. S., and A. A. Aly. "Facile, Three-Component Synthesis of Dithiocarbamate Derivatives With Potent Antimicrobial Activity." Phosphorus, Sulfur, and Silicon and the Related Elements 185, no. 11 (2010): 2194–200. http://dx.doi.org/10.1080/10426500903453300.

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