Relevant bibliographies by topics / Mercapto-1

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Mercapto-1'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Mercapto-1"

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Végh, Daniel, Michal Uher, Oľga Rajniaková, Miloslava Dandárová, and Milan Kováč. "Preparation of vic-Mercaptoisopentanols." Collection of Czechoslovak Chemical Communications 58, no. 2 (1993): 404–8. http://dx.doi.org/10.1135/cccc19930404.

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This paper describes the preparation of some mercaptoisopentanols: 2-mercapto-3-methyl-1-butanol (I), 1-mercapto-3-methyl-2-butanol (II), 3-mercapto-3-methyl-2-butanol (III) and the unsaturated analogue of compound I - 2-mercapto-3-methyl-2-buten-1-ol (IV). These compounds belong to the flavonoid group present in food responsible for deterioration of their gustatory properties.
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Aliya, Sireesha B., Venkata Ramana Reddy Ch., and Sarala Devi Ch. "Spectral and equilibrium studies on some new derivatives of 4-amino-5-phenyl-3-mercapto-1,2,4-triazole." Journal of Indian Chemical Society Vol. 85, Sep 2008 (2008): 926–29. https://doi.org/10.5281/zenodo.5820217.

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Department of Chemistry, Nizam College, Osmania University, Hyderabad-500 001, India <em>E-mail:</em> dr_saraladevich@yahoo.com <em>Manuscript received 1 October 2007, revised 3 June 2008, accepted 17 June 2008</em> 4-Amino-5-phenyl-3-mercapto-1,2,4-triazole (APMT), 4-(4&#39;-methoxy)benzylidineamino-5-phenyl-3-mercapto-1,2,4- triazole (PMBPMT), 4-benzylidineamino-5-phenyl-3-mercapto-1,2,4-triazole (BPMT), 4-(2&acute;-hydroxy)benzyhdmeammo-5-phenyl-3-mercapto-1 2,4-triazole (HBPMT) and 4-amino-5-(4&#39; -nitro)phenyl-3-mercapto-1,2,4-triazole (ANPMT) were synthesized and characterized&nbsp;by
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V., V. RAMANA, YAMUNA K., and SARASWATHI K. "Stability Constants of Metal Complexes of 1,2,4-Triazoles." Journal of Indian Chemical Society Vol. 68, Dec 1991 (1991): 666–67. https://doi.org/10.5281/zenodo.6135029.

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Department of Chemistry. S. V. University, Tirupati-517 502 <em>Manuscript received 21 May 1990, revised 2 December 1991, accepted 6 December 1991</em> The present study reports the stability constants of the metal complexes using bivalent Mn, Fe, Co, Ni, Cu and Zn with 4-amino-3-(methylphenyl)-5- mercapto-1 ,2,4-triazole (1), 4-amino-3-phenyl-5-mercapto-1,2,4-triazole (2), 4-amino-3-(p-cblorophenoxymethyl)-5-mercapto-1,2,4-triazole (3), 4-amino-3&middot; (phenoxymethyl)-5-mercapto-1,2,4-triazole (4).
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Phillips, Brian T., David A. Claremon, and Sandor L. Varga. "Preparation of 5-Substituted 2-Mercapto-1-methylimidazoles. Direct Metalation of 2-Mercapto-1-methylimidazole." Synthesis 1990, no. 09 (1990): 761–63. http://dx.doi.org/10.1055/s-1990-27007.

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Iglesias, Luis E., Alicia Baldessari, and Eduardo G. Gros. "Lipase-catalyzed chemospecific O-acylation of 3-mercapto-1-propanol and 4-mercapto-1-butanol." Bioorganic & Medicinal Chemistry Letters 6, no. 7 (1996): 853–56. http://dx.doi.org/10.1016/0960-894x(96)00133-3.

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IGLESIAS, L. E., A. BALDESSARI, and E. G. GROS. "ChemInform Abstract: Lipase-Catalyzed Chemospecific O-Acylation of 3-Mercapto-1-propanol and 4-Mercapto-1-butanol." ChemInform 27, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.199635043.

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PHILLIPS, B. T., D. A. CLAREMON, and S. L. VARGA. "ChemInform Abstract: Preparation of 5-Substituted 2-Mercapto-1-methylimidazoles. Direct Metalation of 2-Mercapto-1-methylimidazole." ChemInform 22, no. 3 (2010): no. http://dx.doi.org/10.1002/chin.199103169.

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Zhang, Jiaqian, Zhe Wang, Ying Luo, et al. "Preparation and Characterization of Mercapto-Functionalized Calcined Attapulgite and Its Removal of Pb (II) and Cd (II) Solution." Minerals 13, no. 10 (2023): 1337. http://dx.doi.org/10.3390/min13101337.

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To enhance the sorption efficacy of attapulgite for heavy metals, mercapto-functionalized attapulgite (ATP-SH) was synthesized with mercaptan functional groups. When the mass-to-volume ratio of calcined attapulgite (ATP-C) to 3-Mercapropyltrimethoxysilane (MPTMS) was 1 g:0.5 mL (ATP-SH-0.5) and the pH was set to 8, a strong adsorption capacity for Cd (II) and Pb (II) was demonstrated. This indicates excellent adsorption performance for these heavy metals. ATP-SH-0.5 exhibited a maximum adsorption capacity of 43.81 mg/g and 274.83 mg/g for Cd (II) and Pb (II), respectively, in a single ion syst
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Miftiyati, Saral Dwi, Saprini Hamdiani, and Made Ganesh Darmayanti. "Synthesis Of Paramagnetic Merkapto Silica Hybrid From Rice Husk Ash For Ag(I) Adsorben." Acta Chimica Asiana 1, no. 2 (2018): 30. http://dx.doi.org/10.29303/aca.v1i2.19.

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A study has been conducted on the synthesis of paramagnetic mercapto silica hybrids as metal adsorbent of Ag(I). The aim of this study was to synthesis paramagnetic mercapto silica hybrid from rice husk ash waste, knowing the characteristics of paramagnetic mercapto silica hybrid from rice husk ash waste, and to determine the effect of pH, metal ions concentration, and the contact time on the value of adsorption capacity (Q). Based on the results of the study, it was found that paramagnetic mercapto silica hybrids can be synthesized from the rice husk ash waste. Characterization using FTIR spe
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Kupihár, Zoltán, Zoltán Schmél, and Lajos Kovács. "6-S-Trityl-mercapto-hexan-1-ol." Molecules 5, no. 12 (2000): M144. http://dx.doi.org/10.3390/m144.

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Dissertations / Theses on the topic "Mercapto-1"

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Pereira, Fernanda Antonia. "Estudo da interação do As(III) com modelo "zinc finger" da proteína NCp7 HIV-1 e complexos de Bi(III) e Sb(III) com ligantes contendo 2-mercapto-imidazol." Universidade Federal de Minas Gerais, 2010. http://hdl.handle.net/1843/SFSA-8DFJ9Z.

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The ejection of zinc from its coordination site in Zn-finger protein can be promoted by other metal species through competitive binding. This is considered as a promising strategy to inactivate the Zn-finger protein and for the design of new and more efficient drugs. A study of the As(III) interaction with the CCHC zinc finger domain of the NCp7 protein of HIV-1 has been carried out using the fluorescence and circular dichroism spectroscopies. This study allowed a better understanding of the ability of As(III) to promote Zn ejection and brought new insights into the role of glutathione as a bi
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VALLEE, PAULE YOLANDE. "Obtention par thermolyse eclair et etude physicochimique de molecules conjuguees reactives d'interet synthetique ou astrophysique." Caen, 1988. http://www.theses.fr/1988CAEN2033.

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Camacho, Cláudia Sofia. "Polímeros condutores em monocamadas automontadas para a determinação de compostos de interesse ambiental." Master's thesis, 2012. http://hdl.handle.net/10400.13/1663.

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Huang, Sheng-Han, and 黃聖涵. "1. Total Synthesis of (+)-Antrocin 2. Study and Synthesis of Thionated Perylene Diimides for N-Channel Organic Field Effect Transistors3. Thiazo[2,3-a]tetrahydroisoquinolines from Addition Reaction of 3,4-Dihydroisoquinolines with (E)-4-Mercapto-2-butenoic Ester." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/05116601965888128991.

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博士<br>國立暨南國際大學<br>應用化學系<br>105<br>Part 1: This thesis three parts. The frist total synthesis of (+)-antrocin, which was need to clarify the absolute structure of the natural sesquiterpenoid (-)-antrocin. Special transformations in this synthetic route include highly stereoselective intramolecular Diels-Alder reaction (IMDA) of camphanate triene intermediate and highly efficient selective hydrogenation with two different catalysts. We explain the key intramolecular Diels-Alder reaction mechanism by density functional theory calculation. Overall the (+)-anrtocin was synthesized starting from com
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Nyokong, T., K. I. Ozoemena, and B. Agboola. "Synthesis and electrochemical characterisation of benzyl mercapto and dodecylmercapto tetra substituted cobalt, iron, and zinc phthalocyanines complexes." 2006. http://eprints.ru.ac.za/229/1/tebello.pdf.

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The work reports on cyclic voltammetry (CV), square wave voltammetry and spectroelectrochemistry of the following complexes: tetrakis (benzyl mercapto) phthalocyanine complexes of Zn(II) (ZnTBMPc, 4a ), Co(II) (CoTBMPc, 5a ), Fe(II) (FeTBMPc 6a ); and tetrakis (dodecylmercapto) phthalocyanine complexes of Zn(II) (ZnTDMPc, 4b), Co(II) (CoTDMPc, 5b) and Fe(II) (FeTDMPc, 6b). More reversible CV couples were observed for complexes 4a, 5a and 6a containing thiol phenyl ring substituents. Complexes 4b, 5b and 6b containing long chain thiol substituents showed less reversible couples. Complexes 6a
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Books on the topic "Mercapto-1"

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Carné, Josep Vives. Estudi dels complexos formats pels lligands 4-mercapto-1-metilpiperidina, 3-dimetilamino-1-propantiol i 3-amino-1-propantiol amb els ions Ag(I) i Cd(II). 1987.

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Book chapters on the topic "Mercapto-1"

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Trinchieri, A., P. Luongo, F. Rovera, R. Nespoli, G. Zanetti, and E. Austoni. "Treatment of Cystine Nephrolithiasis with Alpha-Mercapto-Propionylglycine." In Urolithiasis 2. Springer US, 1994. http://dx.doi.org/10.1007/978-1-4615-2556-1_236.

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Hussein, Waleed M., Mariusz Skwarczynski, and Istvan Toth. "Double Conjugation Using Mercapto-Acryloyl and Alkyne-Azide Reactions for the Synthesis of Branched Multiantigenic Vaccine Candidates." In Methods in Molecular Biology. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1617-8_13.

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Cvijanović D., Damjanović V., Picek I., and Foretić B. "Spectroscopic studies of methimazole reactivity toward the aquapentacyanoferrate(II) ion in aqueous solutions." In Advances in Biomedical Spectroscopy. IOS Press, 2013. https://doi.org/10.3233/978-1-61499-184-7-085.

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Methimazole (2-mercapto-1-methylimidazole, MMI) and its pentacyanoferrate(II) complex have been characterized by means of UV/Vis, Raman and NMR spectroscopy. The reaction of MMI with aquapentacyanoferrate(II), [Fe(CN)5(H2O)]3&amp;minus;, in buffered aqueous solutions yielded the [Fe(CN)5(MMI)]3&amp;minus;complex. It was found that only thione tautomer of MMI coordinates to the iron(II). The exceptionally stabile and inert complex was produced.
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Yu, Ningya, Junlin Zheng, Qunli Tang, et al. "Preparation of hydrothermally stable mercapto-functionalized mesoporous silicas via assembly of nanoclustered zeolite Y seeds and 3-mercaptopropyltrimethoxysilane." In Nanoporous Materials IV, Proceedings of the 4th International Symposium on Nanoporous Materials. Elsevier, 2005. http://dx.doi.org/10.1016/s0167-2991(05)80210-1.

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Conference papers on the topic "Mercapto-1"

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Robbins, Winston, Sridhar Srinivasan, and Gerrit Buchheim. "Predicting Hot Oil Corrosion: a Framework for Quantifying Reactive Organic Sulfur Compounds in Crude Unit Process Streams." In CONFERENCE 2023. AMPP, 2023. https://doi.org/10.5006/c2023-19105.

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Abstract Sulfur has long been recognized to contribute to many forms of corrosion in petroleum refining. One of the most common and least understood forms of corrosion is hot oil sulfidation, i.e., localized wall thinning by reactive organic sulfur compounds (ROSC) in CDU and VDU operations. In oil at 400-750F (204-400C), Simultaneous Naphthenic Acid alongside Sulfidation (SNAPS) reactions remove iron (Fe) from steel surfaces. Discrepancies in observed corrosion among refinery operators (through inspection) and laboratory testing are frequently due to differences in sulfur analyses of oils. In
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Patel, Ishan, Gheorghe Bota, and David Young. "Evaluation of Reactive Sulfur for Improved Corrosion Predictions in Oil Refineries." In CONFERENCE 2022. AMPP, 2022. https://doi.org/10.5006/c2022-18039.

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Abstract Refinery operators rely on total sulfur (TS) content (wt.% S) and total acid number (TAN), reported in crude oil assays, to predict high temperature corrosion rates by organosulfur species and naphthenic acids. The sulfur exists in a variety of forms in crude oil, associated with particular molecular moieties; from the standpoint of corrosion, these are grouped into reactive (sulfide and mercaptan) and non-reactive (thiophenic) species. According to an industrial rule-of-thumb, only 1/3 of the TS is considered as reactive sulfur (RS) and, hence, this value, together with TAN, is typic
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Reddy, D. Amaranatha, G. Murali, R. P. Vijayalakshmi, et al. "2-Mercapto Ethanol Passivated Zn[sub 1−x]Cr[sub x]S Nanoparticles." In SOLID STATE PHYSICS, PROCEEDINGS OF THE 55TH DAE SOLID STATE PHYSICS SYMPOSIUM 2010. AIP, 2011. http://dx.doi.org/10.1063/1.3605834.

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Cvetković, Aleksandar, Mihajlović Petrović, Žaklina Tasić, Milan Radovanović, Ana Simonović, and Vladan Nedelkovski. "Influence of organic compound structure on brass corrosion inhibition efficiency." In Proceedings of XVI International Mineral Processing and Recycling Conference, Belgrade, 28-30.05.2025. University of Belgrade, Technical Faculty, Bor, 2024. https://doi.org/10.5937/imprc25497c.

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In this study the influence of organic compounds with different structures on the inhibition of brass corrosion in sodium chloride solutions of 0.9%, 2% and 3.5% is investigated. The experimental work includes the evaluation of the inhibition efficiency of 2-mercapto-1-methylimidazole (MMI), 2-amino-5-ethyl1,3,4-thiadiazole (AETDA) and N-acetyl-L-leucine at various concentrations using electrochemical methods, including open circuit potential (OCP), cyclic voltammetry (CV), and potentiodynamic measurements (PD). The results show that all tested inhibitors reduce the corrosion currents and pote
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Kawaguchi, Touru, Gota Kikugawa, Ikuya Kinefuchi, Taku Ohara, Shinichi Yatuzuka, and Yoichiro Matsumoto. "Molecular Dynamics Study of Interfacial Thermal Resistance of Mercapto-Alkanol Self-Assembled Monolayer and Water." In ASME 2009 Second International Conference on Micro/Nanoscale Heat and Mass Transfer. ASMEDC, 2009. http://dx.doi.org/10.1115/mnhmt2009-18424.

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The interfacial thermal resistance of 11-mercaptoundecanol (-S(CH2)11OH) self-assembled monolayer (SAM) adsorbed on Au(111) substrate and water was investigated using nonequilibrium molecular dynamics simulations. The interfacial thermal resistance was found to be a half of that in the system which consists of 1-dodecanthiol (-S(CH2)11CH3) SAM adsorbed on Au(111) and toluene [Kikugawa G. et al., J. Chem. Phys. (2009)]. The effective thermal energy transfer originates from hydrogen-bond structure between the SAM and water molecules in spite of weak structurization of water molecules near the SA
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Spang, Brent, Sayaka Yoshimura, Richard Hack, Vincent McDonell, and Scott Samuelsen. "Evaluation of the Level of Gaseous Fuel-Bound Sulfur on Fine Particulate Emission From a Low Emission Gas Turbine Engine." In ASME Turbo Expo 2012: Turbine Technical Conference and Exposition. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/gt2012-69352.

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The present work investigates the effect of natural gas fuel sulfur on particulate emissions from stationary gas turbine engines used for electricity generation. Fuel sulfur from standard line gas was scrubbed using a system of fluidized reactor beds containing a specially designed activated carbon purposely built for sulfur absorption. A sulfur injection system using sonic orifices was designed and constructed to inject methyl mercaptan into the scrubbed gas stream at varying concentrations. Using these systems, particulate emissions created by various fuel sulfur levels between 0 and 15 ppmv
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