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Littérature scientifique sur le sujet « Organotin compounds »

Auteur : Grafiati
Publié le 4 juin 2021
Mis à jour le 25 juillet 2025

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Articles de revues sur le sujet "Organotin compounds"

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White, Jane S., John M. Tobin, and Joseph J. Cooney. "Organotin compounds and their interactions with microoganisms." Canadian Journal of Microbiology 45, no. 7 (1999): 541–54. http://dx.doi.org/10.1139/w99-048.

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Organotin compounds are ubiquitous in the environment. The general order of toxicity to microorganisms increases with the number and chain length of organic groups bonded to the tin atom. Tetraorganotins and inorganic tin have little toxicity. Because of their lipophilicity, organotins are regarded as membrane active. There is evidence that the site of action of organotins may be both at the cytoplasmic membrane and intracellular level. Consequently, it is not known whether cell surface adsorption or accumulation within the cell, or both is a prerequisite for toxicity. Biosorption studies on a
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Podestá, J. C., A. B. Chopa, A. D. Ayala, and L. C. Koll. "Organotin compounds." Journal of Organometallic Chemistry 333, no. 1 (1987): 25–36. http://dx.doi.org/10.1016/s0022-328x(00)99028-4.

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Ayala, A. D., N. Giagante, J. C. Podestá, and W. P. Neumann. "Organotin compounds." Journal of Organometallic Chemistry 340, no. 3 (1988): 317–29. http://dx.doi.org/10.1016/0022-328x(88)80025-1.

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Podestá, Julio C., Alicia D. Ayala, Alicia B. Chopa, and Nelda N. Giagante. "Organotin compounds." Journal of Organometallic Chemistry 364, no. 1-2 (1989): 39–55. http://dx.doi.org/10.1016/0022-328x(89)85329-x.

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Martin, F., FM Corrigan, Ofx Donard, J. Kelly, Jao Besson, and DF Horrobin. "Organotin compounds in trimethyltin-treated rats and in human brain in Alzheimer's Disease." Human & Experimental Toxicology 16, no. 9 (1997): 512–15. http://dx.doi.org/10.1177/096032719701600906.

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As blood tin concentrations are elevated in Alzheimer's disease and as some low molecular weight organotin compounds are neurotoxic, we have attempted to detect organotins in brain in Alzheimer's Disease. First we measured the concentration of trimethyltin (TMT) in the brains of rats which had been exposed to memory- impairing concentrations of TMT and, as the method of linking hydride generation, cryogenic trapping, gas chromatographic separation and atomic absorption spec trophotometric detection permitted the measurements of organotin compounds when the total tin was greater than 0.2 nanogr
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Terraza, V. Fabricio, Darío C. Gerbino, and Julio C. Podestá. "Stereoselective Hydrostannation of Diacrylate and Dimethacrylate Esters of Galactaric Acid Derivatives: Cyclohydrostannation vs. Diaddition." Proceedings 9, no. 1 (2018): 55. http://dx.doi.org/10.3390/ecsoc-22-05688.

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This paper reports a study on the free radical hydrostannation of ((4S,4′R,5R,5′S)-2,2,2′,2′-tetramethyl-[4,4′-bi(1,3-dioxolane)]-5,5′-diyl)bis(diphenyl methylene) diacrylate (1) and dimethacrylate (2) with triorganotin hydrides, R3SnH (R = Me, n-Bu, Ph). Preliminary investigations show that these reactions could lead to mixtures of products of cyclohydrostannation and/or mono- or diaddition according to the organotin hydrides employed and the reaction conditions used. The addition of Me3SnH to 1 afforded a mixture of three organotin compounds from which the pure new 13-membered macrodiolide 3
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Cheng, Shuming, and Jing Yang. "A Theoretical Study of Organotin Binding in Aromatase." International Journal of Molecular Sciences 24, no. 10 (2023): 8954. http://dx.doi.org/10.3390/ijms24108954.

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The widely used organotin compounds are notorious for their acute toxicity. Experiments revealed that organotin might cause reproductive toxicity by reversibly inhibiting animal aromatase functioning. However, the inhibition mechanism is obscure, especially at the molecular level. Compared to experimental methods, theoretical approaches via computational simulations can help to gain a microscopic view of the mechanism. Here, in an initial attempt to uncover the mechanism, we combined molecular docking and classical molecular dynamics to investigate the binding between organotins and aromatase.
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Fent, Karl. "Ecotoxicology of Organotin Compounds." Critical Reviews in Toxicology 26, no. 1 (1996): 3–117. http://dx.doi.org/10.3109/10408449609089891.

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Fait, Antonella, Adalberto Ferioli, and Franco Barbieri. "Chapter 11 Organotin compounds." Toxicology 91, no. 1 (1994): 77–82. http://dx.doi.org/10.1016/0300-483x(94)90244-5.

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Appel, Klaus E. "Organotin Compounds: Toxicokinetic Aspects." Drug Metabolism Reviews 36, no. 3-4 (2004): 763–86. http://dx.doi.org/10.1081/dmr-200033490.

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Thèses sur le sujet "Organotin compounds"

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Clarke, David John. "Organotin compounds for catalysis." Title page, abstract and contents only, 2001. http://web4.library.adelaide.edu.au/theses/09SM/09smc5974.pdf.

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Hill, Michael Stephen. "Organotin tetrazoles and related compounds." Thesis, University of Bath, 1994. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.240694.

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Kuan, Fong Sheen, and mikewood@deakin edu au. "Organotin-Oxo Clusters." Deakin University. School of biological and chemical sciences, 2002. http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20051125.084244.

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This thesis reports on the development and expansion of reliable synthetic di-and multi-tin precursors for the assembly of oligomeric organotin-oxo compounds in which the shape, dimension and tin nuclearity can be controlled. The reaction of polymeric diorganotin oxides, (R2SnO)m (R = Me, Et, n-Bu, n-Oct, c-Hex, i-Pr, Ph), with saturated aqueous NH4X solutions (X = F, Cl, Br, I, OAc) in refluxing 1,4-dioxane afforded in high yields dimeric tetraorganodistannoxanes, [R2(X)SnOSn(X)R2]2, and in a few cases diorganotin dihalides or diacetates, R2SnX2. This method appears to be particularly good fo
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Al-Rawi, Mustafa. "Halogenation of sterically hindered organotin compounds." Thesis, University of Sussex, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.310661.

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Chatterjee, Debesh Kumar. "Arylazo phenoxy derivatives of organotin compounds." Thesis, University of North Bengal, 1990. http://hdl.handle.net/123456789/757.

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Ross, Jennifer Nicola. "Alkoxy- substituted aryl- and benzyl- organotin compounds." Thesis, University of Aberdeen, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324880.

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New organotin compounds containing alkoxy- functionalities have been prepared. The methods of preparation of the tetraorganotin species have involved three routes. Hydrostannation reactions using triphenyltin hydride have resulted in the synthesis of triphenyltin derivatives of a series of alkoxy- substituted allyl ethers. The addition of tin IV chloride, diphenyltin dichloride and phenyltin trichloride to alkoxy- substituted aryl- and benzyl- Grignard reagents have also been successful. Alkoxy- substituted benzyltin compounds have been prepared by following an alternative preparation of benzy
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Deb, Chaitali. "Preparation and reactions of some organotin compounds : applications to organic synthesis." Thesis, University of North Bengal, 1993. http://hdl.handle.net/123456789/759.

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Doidge-Harrison, Solange Maria Silva Veloso. "X-ray and spectroscopic studies of organotin compounds." Thesis, Robert Gordon University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.304984.

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O'Loughlin, Edward John. "Association of organotin compounds with aquatic humic substances /." The Ohio State University, 1997. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487946776023338.

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Baguley, Paul A. "Search for practical alternatives to organotin hydrides." Thesis, University of St Andrews, 1998. http://hdl.handle.net/10023/15419.

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A summary of the tin hydride method of generating radicals in organic synthesis is presented, followed by illustrative examples of other methods available for mediating radical reactions, with a particular emphasis on recent developments. This is followed by four chapters describing our efforts to introduce alternative methods for generating radicals. A range of l-alkylcyclohexa-2,5-diene-l-carboxylic acids have been prepared by Birch reduction-alkylation methodology and shown to generate the corresponding alkyl radical by thermal initiation with dibenzoyl peroxide. The 1-benzyl, cyclopentyl a
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Livres sur le sujet "Organotin compounds"

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Schumann, Herbert, and Ingeborg Schumann. Sn Organotin Compounds. Edited by Ulrich Krüerke. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-662-06612-6.

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Schumann, Herbert, and Ingeborg Schumann. Sn Organotin Compounds. Edited by Ulrich Krüerke. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-662-09147-0.

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Schumann, Herbert, Ingeborg Schumann, Rainer Bohrer, Bernd Kalbskopf, and Hans-Jürgen Richter-Ditten. Sn Organotin Compounds. Edited by Ulrich Krüerke. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-662-09150-0.

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Schumann, Herbert, and Ingeborg Schumann. Sn Organotin Compounds. Edited by Ulrich Krüerke. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-662-09165-4.

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Schumann, Herbert, and Ingeborg Schumann. Sn Organotin Compounds. Edited by K. C. Buschbeck, H. Bergmann, J. Füssel, et al. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-662-06750-5.

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Canada, Canada Environment, Canada. Health and Welfare Canada., and Canada, eds. Non-pesticidal organotin compounds. Environment Canada, 1993.

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Davies, Alwyn George. Organotin chemistry. 2nd ed. Wiley-VCH, 2004.

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Davies, Alwyn George. Organotin chemistry. 2nd ed. VCH, 2004.

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Evans, Colin J. Organotin compounds in modern technology. Elsevier, 1985.

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R, Blair W., and United States. National Bureau of Standards, eds. An International butyltin measurement methods intercomparison: Sample preparation and results of analyses. U.S. Dept. of Commerce, National Bureau of Standards, 1986.

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Chapitres de livres sur le sujet "Organotin compounds"

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Schumann, Herbert, and Ingeborg Schumann. "Organotin Compounds." In Sn Organotin Compounds. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-662-09147-0_1.

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Schumann, Herbert, Ingeborg Schumann, Rainer Bohrer, Bernd Kalbskopf, Hans-Jürgen Richter-Ditten, and Ulrich Krüerke. "Organotin Compounds." In Sn Organotin Compounds. Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-662-09150-0_1.

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Schumann, Herbert, and Ingeborg Schumann. "Organotin Compounds." In Sn Organotin Compounds. Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-662-09165-4_1.

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Blunden, Stephen J., and Colin J. Evans. "Organotin Compounds." In The Handbook of Environmental Chemistry. Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-540-46211-8_1.

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Schumann, Herbert, Ingeborg Schumann, K. C. Buschbeck, et al. "Organotin Compounds." In Sn Organotin Compounds. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-662-06750-5_1.

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Fugami, Keigo, and Masanori Kosugi. "Organotin Compounds." In Topics in Current Chemistry. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-45313-x_4.

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Schumann, Herbert, Ingeborg Schumann, and Ulrich Krüerke. "Organotin Compounds." In Sn Organotin Compounds. Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-662-06612-6_1.

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Champ, Michael A., and Terry L. Wade. "Regulatory Policies and Strategies for Organotin Compounds." In Organotin. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-1507-7_3.

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Laughlin, Roy B., John Thain, Brad Davidson, Aldis O. Valkirs, and Frederick C. Newton. "Experimental Studies of Chronic Toxicity of Tributyltin Compounds." In Organotin. Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-1507-7_10.

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Lee, Maw-Rong, and Chung-Yu Chen. "Organotin Compounds Analysis." In Analysis of Endocrine Disrupting Compounds in Food. Wiley-Blackwell, 2012. http://dx.doi.org/10.1002/9781118346747.ch11.

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Actes de conférences sur le sujet "Organotin compounds"

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Kaluđerović, Goran. "MESOPOROUS SILICA AS A VEHICLE FOR ORGANOTIN(IV) COMPOUNDS." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac,, 2021. http://dx.doi.org/10.46793/iccbi21.060k.

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Free Ph3Sn(CH2)nOH (n = 3, 4, 6, 8 and 11) and immobilized organotin(IV) compounds, SBA- 15~Cl|Ph3Sn(CH2)nOH, were prepared and tested against different tumor cell lines. Both compounds and nanomaterials revealed strong cytotoxic potential. SBA-15~Cl|Ph3Sn(CH2)3OH as well as free compound induce caspase triggered apoptosis in human ovarian A2780 cells. Ph3Sn(CH2)6OH and corresponding nanomaterial induced apoptosis in mouse melanoma B16 cells. Survived clones of B16 cells demonstrated phenotypic changes, they differentiate toward melanocytes.
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Humphrey, B., and D. Hope. "Analysis of Water, Sediments, and Biota for Organotin Compounds." In OCEANS '87. IEEE, 1987. http://dx.doi.org/10.1109/oceans.1987.1160626.

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Becker, Til J., Tamara Krajnović, Vuk Gordić, et al. "TETRAKIS(4-METHOXYBENZENE)TIN(IV) IMMOBILISED INTO MCM-41 AND SBA-15 MESOPOROUS NANOSTRUCTURES." In 17th International Conference on Fundamental and Applied Aspects of Physical Chemistry. Society of Physical Chemists of Serbia, 2024. https://doi.org/10.46793/phys.chem24i.285b.

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Tetraaryltin(IV) compounds are suitable compounds to replace platinum-based chemotherapeutics since they provide promising in vitro results. To further decrease toxicity and side effects, passive drug targeting via nanostructures can be utilised, since tumour tissues provide the ability to accumulate bigger particles than healthy ones. In this study, tetrakis(4-methoxybenzene)tin(IV) (1) is immobilised in two mesoporous silica nanostructures (MCM-41|1 and SBA-15|1), which are synthesised and characterised herein. Employing MTT and CV assays, the antitumour activity of the organotin(IV) compoun
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Young, D., P. Schatzberg, F. Brinckman, M. Champ, S. Holm, and R. Landy. "Summary Report - Interagency Workshop on Aquatic Sampling and Analysis for Organotin Compounds." In OCEANS '86. IEEE, 1986. http://dx.doi.org/10.1109/oceans.1986.1160347.

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Cherek, Paulina, Michaela Balogova, Krishna Damodaran, and Helga M. Ögmundsdottir. "Abstract 2807: Cytotoxic activity of novel organotin compounds against different cancer cell lines." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-2807.

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Ivanovski, Vladimir, Til Becker, Ivana Predarska, Evamarie Hey-Hawkins, and Goran N. Kaluđerović. "IR and Raman spectroscopy: monitoring immobilization of some anticancer organotin(IV) compounds on mesoporous silica." In Biomedical Spectroscopy, Microscopy, and Imaging III, edited by Jürgen Popp and Csilla Gergely. SPIE, 2024. http://dx.doi.org/10.1117/12.3029524.

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Massari, Federica, Pietro Cotugno, Angelo Tursi, et al. "Mapping of Organotin compounds in sediments of Mar Piccolo (Taranto, Italy) using Gas Chromatography-Mass Spectrometry analysis and geochemical data." In 2021 International Workshop on Metrology for the Sea; Learning to Measure Sea Health Parameters (MetroSea). IEEE, 2021. http://dx.doi.org/10.1109/metrosea52177.2021.9611609.

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Ciavell, C., P. Seligman, and P. Stang. "Automated Analysis of Organotins Compounds: A Method for Monitoring Butyltins in the Marine Environment." In OCEANS '86. IEEE, 1986. http://dx.doi.org/10.1109/oceans.1986.1160368.

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Pitta, Marina Galdino da Rocha, Jordy Silva de Carvalho, Luzilene Pereira de Lima, and Ivan da Rocha Pitta. "iPSC therapies applied to rehabilitation in parkinson’s disease." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.022.

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Background: Parkinson’s disease (PD) is a neurological disorder that affects movement, mainly due to damage and degeneration of the nigrostriatal dopaminergic pathway. The diagnosis is made through a clinical neurological analysis where motor characteristics are considered. There is still no cure, and treatment strategies are focused on symptoms control. Cell replacement therapies emerge as an alternative. Objective: This review focused on current techniques of induced pluripotent stem cells (iPSCs). Methods: The search terms used were: “Parkinson’s Disease”, “Stem cells” and “iPSC”. Open arti
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