Relevant bibliographies by topics / Sulfinic acids

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

Academic literature on the topic 'Sulfinic acids'

Author: Grafiati
Published: 4 June 2021
Last updated: 27 January 2023

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Journal articles on the topic "Sulfinic acids"

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Vicente, Dmistocles A., Danilo Galdino, Marcelo Navarro, and Paulo H. Menezes. "Electrochemical synthesis of sulfonamides in a graphite powder macroelectrode." Green Chemistry 22, no. 16 (2020): 5262–66. http://dx.doi.org/10.1039/d0gc01360a.

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And, Chew Lee, and Lamar Fields. "SULFINIC ACIDS AND RELATED COMPOUNDS. 21. PREPARATION OF CRYSTALLINE SULFINIC ESTERS1,2." Phosphorus, Sulfur, and Silicon and the Related Elements 45, no. 1-2 (September 1989): 35–45. http://dx.doi.org/10.1080/10426508908046074.

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ZOLLER, U. "ChemInform Abstract: Syntheses of Sulfinic Acids." ChemInform 22, no. 40 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199140281.

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Herwig, Jürgen, and Wilhelm Keim. "Palladium complex catalysed synthesis of sulfinic acids, sulfinic acid esters, sulfonic acids and S-alkyl alkanethiosulfonates." Inorganica Chimica Acta 222, no. 1-2 (July 1994): 381–85. http://dx.doi.org/10.1016/0020-1693(94)03911-9.

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Lee, Chew, D. Brian Stidham, and Lamar Field. "SULFINIC ACIDS AND RELATED COMPOUNDS. 22. DERIVATIVES OF 2-HYDROXYETHANE SULFINIC ACID1,2." Phosphorus, Sulfur, and Silicon and the Related Elements 47, no. 1-2 (January 1990): 53–59. http://dx.doi.org/10.1080/10426509008046846.

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STIRLING, C. J. M. "ChemInform Abstract: Sulfinic Acids and Carboxylic Acids - a Comparison." ChemInform 22, no. 41 (August 22, 2010): no. http://dx.doi.org/10.1002/chin.199141299.

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Liu, Cong-Rong, and Liang-Hui Ding. "Byproduct promoted regioselective sulfenylation of indoles with sulfinic acids." Organic & Biomolecular Chemistry 13, no. 8 (2015): 2251–54. http://dx.doi.org/10.1039/c4ob02575j.

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Ivanova, S., and D. Aleksiev. "Addition of Sulfinic Acids to Methacrylic Derivatives." Phosphorus, Sulfur, and Silicon and the Related Elements 186, no. 1 (December 30, 2010): 38–43. http://dx.doi.org/10.1080/10426501003776947.

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Ivanova, Sonya. "Reaction of Sulfinic Acids with Heteroconjugated Alkenes." Phosphorus, Sulfur, and Silicon and the Related Elements 188, no. 11 (September 20, 2013): 1670–74. http://dx.doi.org/10.1080/10426507.2012.760562.

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Kotomkin, A., N. Rusakova, V. Turovtsev, Yu Orlov, and E. Chernova. "Scale of the electronegativities of sulfinic acids." Актуальные направления научных исследований XXI века: теория и практика 2, no. 5 (December 2, 2014): 91–94. http://dx.doi.org/10.12737/6759.

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Dissertations / Theses on the topic "Sulfinic acids"

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Svarovsky, Serge A. "Structure, stability and reactivity of small organic sulfinic and sulfonic acids toxicological implications ; Role of charge transfer complexes in oxidation cleavage of benzpinacols by iron (III) trispenanthroline /." Morgantown, W. Va. : [West Virginia University Libraries], 2000. http://etd.wvu.edu/templates/showETD.cfm?recnum=1231.

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Sun, Xiaowei. "Protective role of coronary endothelium during the development of cardiac hypertrophy insights from pharmacological intervention studies /." Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2008. https://www.mhsl.uab.edu/dt/2010r/xsun.pdf.

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Motto, John M. "Ã,ß-unsaturated sulfoxides and sulfinic acid derivatives." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ58363.pdf.

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Orndorff, Zenah Wilson. "Evaluation of Sulfidic Materials in Virginia Highway Corridors." Diss., Virginia Tech, 2001. http://hdl.handle.net/10919/29183.

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Road construction through sulfidic materials in Virginia has resulted in localized acid rock drainage (ARD) that threatens water quality, fill stability, integrity of building materials, and vegetation management. The objectives of this study were: i) to develop a state-wide sulfide hazard rating map based on characterization of the geologic formations associated with acid roadcuts, ii) to estimate depth to sulfidic sediments in the Coastal Plain based on landscape relationships, and iii) to evaluate potential acidity testing procedures on diverse materials. Geologic formations associated with acid roadcuts were characterized by potential peroxide acidity (PPA) and S content, and grouped into four categories. Listed in order of increasing severity, these formations included: the Tabb Formation (Coastal Plain), the Lynchburg Group of the Ashe Formation (Blue Ridge), the Chesapeake Group and Lower Tertiary deposits (Coastal Plain), the Millboro shale, Marcellus shale, Chatanooga shale and Needmore Formation (Valley and Ridge), and the Quantico Formation (Piedmont). Evaluation of landscape parameters near Richmond, Virginia, indicated that the likelihood of encountering sulfidic materials within a given depth at a specific location was related to elevation and mapped soil types. Elevation and soil map units were assigned to risk classes to indicate the likelihood of encountering sulfides within a depth of 9 m. Comparison of PPA and S content for 296 diverse samples indicated that S may serve as a screening tool to evaluate materials without carbonates. Comparison of PPA and conventional Acid-Base Accounting (ABA) for 14 diverse samples indicated that PPA and ABA were highly correlated, with PPA yielding 0.60 to 0.95X the amount of acidity as ABA. Potential acidity by Soxhlet extraction and PPA were equivalent for 3 of 4 diverse samples. Average acidity and metal contents of leachate from Soxhlet extractors were correlated with acidity and metals of road drainage. Sulfide hazard analysis should be an essential step in the pre-design phase of highway construction and other earth-disturbing activities.
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Boukhenouna, Samia. "Enzymologie des étapes clés de régulation du système Peroxyrédoxine / Sulfirédoxine dans le contexte de la signalisation cellulaire redox." Thesis, Université de Lorraine, 2014. http://www.theses.fr/2014LORR0251/document.

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Les peroxyrédoxines (Prx) sont des peroxydases à thiol, ubiquitaires, qui jouent un rôle central dans la physiologie du peroxyde d’hydrogène. Une famille de Prx dite "2-Cys-Prx typique" possède une propriété unique de suroxydation de la Cys catalytique sous forme acide sulfinique, qui constitue un mécanisme de régulation des fonctions des 2-Cys-Prx typiques en tant que peroxydase, capteur de peroxyde ou protéine chaperon. La réduction des 2-Cys-Prx typiques suroxydées est catalysée par la Sulfirédoxine (Srx), une sulfinyl réductase ATP-dépendante dont la constante catalytique est de l’ordre de 1-2 min-1, une valeur faible qui doit être corrélée au rôle de Srx dans la régulation redox. L’objectif de ce travail était d’analyser l’enzymologie de la régulation du système Prx/Srx au niveau, du processus de suroxydation des 2-Cys-Prx typiques, de l’étape limitante de la Srx, et de son recyclage par les systèmes redox cellulaires. Dans un premier temps, nous avons caractérisé les deux étapes du cycle catalytique de la 2-Cys-Prx typique majeure de S. cerevisiae Tsa1, dont la compétition contrôle la sensibilité à la suroxydation, par une stratégie combinant cinétiques rapides, système enzymatique couplé et modélisation cinétique. Ces travaux suggèrent que cette compétition est contrôlée par une réorganisation conformationnelle au cours du cycle catalytique de la Tsa1. Dans un second temps, l’étude de la première étape du mécanisme catalytique de Srx, qui consiste en l’activation ATP-dépendante du groupement acide sulfinique de la 2 Cys-Prx a permis, i) de montrer que l’étape limitante de la réaction catalysée par Srx était associée au processus chimique de transfert de phosphate, et ii) de proposer un modèle d’assemblage du complexe Michaelien Prx/Srx/ATP formé lors de ce processus. Enfin, par une approche combinant cinétiques enzymatiques in vitro et génétique de la levure in vivo, nous avons établi que le mécanisme de recyclage des Srx à 1 Cys existant chez les plantes ou les mammifères implique le rôle du glutathion comme réducteur cellulaire, contrairement à la Srx de S. cerevisiae qui est recyclée par le système thiorédoxine. De façon inattendue, la spécificité du glutathion dans ce mécanisme est assurée par un événement de reconnaissance au sein du complexe Prx/Srx
The peroxiredoxins (Prx) are ubiquitous thiol peroxidases, which play a central role in the physiology of hydrogen peroxide. A subclass of Prx called "typical 2-Cys-Prx" has a unique property to hyperoxidize the catalytic Cys into the sulfinic acid form, which acts as a regulation mechanism of their functions, as peroxidase, peroxide sensor or protein chaperone. The reduction of the overoxidized form is catalyzed by sulfiredoxin (Srx), an ATP-dependent sulfinyl reductase whose catalytic constant is about 1-2 min-1, a low value that must be correlated to the role of Srx in redox regulation. The aim of this study was to analyze the enzymology of the regulation of the Prx/Srx system at three diffrents points of control: the hyper-oxidation process of typical 2-Cys-Prx, the rate-limiting step of the Srx mechanism and the recycling step of Srx by the cellular thiol redox systems. We have first characterized the competition mechanism between the two steps of the catalytic mechanism of the major typical 2-Cys-Prx of S. cerevisiae, Tsa1, through a strategy combining rapid kinetics, coupled enzyme system and kinetic modelling analysis. This work suggests that the sensitivity to hyper-oxidation is controlled by a conformational reorganization during the catalytic cycle of Tsa1. Next, the study of the first step of Srx catalytic mechanism, which involves the ATP-dependent activation of the sulfinic acid form of typical 2-Cys Prx i) has shown that the rate-limiting step is associated with the chemical phosphate transfer process, and ii) provided an assembly model of the Michaelien complex Prx/Srx/ATP, formed during this process. Finally, through the combination of in vitro enzyme kinetics and in vivo yeast genetic tools, we established that the recycling mechanism of one Cys Srx, existing in plants or mammals, involves the glutathione (GSH) as reducer in cells, contrary to the Srx from S. cerevisiae, which is recycled by the Thioredoxin system. Unexpectedly, our study suggests that GSH binds the thiolsulfinate complex, confirming the role of GSH as the primary reducing system of 1-Cys-Srx
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Kriznik, Alexandre. "Enzymologie du mécanisme de régulation des Peroxyrédoxines par suroxydation au cours de la signalisation cellulaire redox." Thesis, Université de Lorraine, 2020. http://www.theses.fr/2020LORR0083.

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La suroxydation des peroxyrédoxines (Prx) est un mécanisme post-traductionnel essentiel impliqué dans la régulation et la signalisation cellulaire redox. Les Prx sont des peroxydases à thiol, qui réagissent avec les peroxydes pour former un intermédiaire acide sulfénique. Leur sensibilité à la suroxydation dépend de la compétition entre la réaction de sulfinylation et la formation d’un pont disulfure au cours du cycle peroxydase. Cette compétition est contrôlée par une transition conformationnelle entre deux conformations FF : structurée et LU : localement déstructurée. Dans ce projet, nous abordons le mécanisme de suroxydation de Tsa1, la principale Prx1 cytosolique de S. cerevisiae, par des analyses cinétiques à l'état pré-stationnaire en cinétique rapide, à l'état stationnaire et in vivo. Une phase cinétique correspondant à un changement de conformation associé à la transition FF/LU a été identifiée, montrant que la formation de l’acide sulfénique facilite cette transition. L’utilisation de mutants de sensibilité à la suroxydation altérée et de différents substrats peroxydes a permis de montrer que la sensibilité est découplée de l'étape de formation du pont disulfure et ne dépend que des constantes de vitesse de sulfinylation et de transition conformationnelle FF/LU. A partir de ces deux paramètres, nous pouvons prédire l'indice de sensibilité à la suroxydation CHyp1%, une prédiction démontrée in vitro et in vivo
Peroxiredoxins from the Prx1 subfamily (Prx) are moonlighting peroxidases that operate in peroxide signaling and are regulated by sulfinylation. Prxs offer a major model of protein−thiol oxidative modification. They react with H2O2 to form a sulfenic acid intermediate that either engages into a disulfide bond, committing the enzyme into its peroxidase cycle, or again reacts with peroxide to produce a sulfinic acid that inactivates the enzyme. Sensitivity to sulfinylation depends on the kinetics of these two competing reactions and is critically influenced by a structural transition from a fully folded (FF) to locally unfolded (LU) conformation. Analysis of the reaction of the Tsa1 Saccharomyces cerevisiae Prx with H2O2 by Trp fluorescence-based rapid kinetics revealed a process linked to the FF/LU transition that is kinetically distinct from disulfide formation and suggested that sulfenate formation facilitates local unfolding. Use of mutants of distinctive sensitivities and of different peroxide substrates showed that sulfinylation sensitivity is not coupled to the resolving step kinetics but depends only on the sulfenic acid oxidation and FF-to-LU transition rate constants. From these two parameters, the relative sensitivities of Prxs toward hyperoxidation with different substrates can be predicted, as confirmed by in vitro and in vivo patterns
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Liu, Pingyang. "Biochemical studies of enzymes in insect cuticle hardening." Diss., Virginia Tech, 2013. http://hdl.handle.net/10919/50528.

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In insects, the cuticle provides protection against physical injury and water loss, rigidness for muscle attachment and mechanical support, and flexibility in inter-segmental and joint areas for mobility. As most insects undergo metamorphosis, they need to shred off old cuticle and synthesize new cuticle to fit the body shape and size throughout their life cycles. The newly formed cuticle, mainly composed of cuticular proteins, chitin, and sclerotizing reagents, needs to be hardened through the crosslinks between cuticular proteins and sclerotizing reagents. This dissertation concerns the biochemical activities of several pyridoxal 5-phosphate (PLP)-dependent decarboxylases with most of them involved in insect cuticle hardening. Herein, we first present a detailed overview of topics in reactions and enzymes involved in insect cuticle hardening. Aspartate 1-decarboxylase (ADC) is at the center of this dissertation. beta-alanine, the product of ADC-catalyzed reaction from aspartate, is the component of an important sclerotizing reagent, N-beta-alanyldopamine; the levels of beta-alanine in insects regulate the concentrations of dopamine, therefore affecting insect sclerotization and tanning (collectively referred as cuticle hardening in this dissertation).

Biochemical characterization of insect ADC has revealed that this enzyme has typical mammalian cysteine sulfinic acid decarboxylase (CSADC) activity, able to generate hypotaurine and taurine. The result throws lights on research in the physiological roles of insect ADC and the pathway of insect taurine biosynthesis. Cysteine was found to be  an inactivator of several PLP-dependent decarboxylases, such as ADC, glutamate decarboxylase (GAD) and CSADC. This study helps to understand symptoms associated with the abnormal cysteine concentrations in several neurodegenerative diseases. A mammalian enzyme, glutamate decarboxylase like-1 (GADL1), has been shown to have the same substrate usage as insect ADC does, potentially contributing to the biosynthesis of taurine and/or beta-alanine in mammalian species. Finally, the metabolic engineering work of L-3, 4-dihydroxyphenylalanine decarboxylase (DDC) and 3, 4-dihydroxylphenylacetaldehyde (DHPAA) synthase has revealed that the reactions of these enzymes could be determined by a few conserved residues at their active site. As both enzymes have been implicated in the biosynthesis of sclerotizing reagents, it is of great scientific and practical importance to understand the similarity and difference in their reaction mechanisms. The results of this dissertation provide valuable biochemical information of ADC, DDC, DHPAA synthase, and GADL1, all of which are PLP-dependent decarboxylases. ADC, DDC, DHPAA synthase are important enzymes in insect cuticle hardening by contributing to the biosynthesis of sclerotizing reagents. Knowledge towards understanding of these enzymes will promote the comprehension of insect cuticle hardening and help scientists to search for ideal insecticide targets. The characterization of GADL1 lays groundwork for future research of its potential role in taurine and beta-alanine metabolism.

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Roussel, Xavier. "Enzymologie moléculaire d'une sulfinyl réductase, la sulfirédoxine : Caractérisation du mécanisme catalytique." Thesis, Nancy 1, 2009. http://www.theses.fr/2009NAN10082/document.

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Les peroxyrédoxines à deux cystéines typiques (2-Cys Prx) sont impliquées dans la résistance des cellules au stress oxydant associé à H2O2, en réduisant H2O2 en H2O. En parallèle, ces enzymes participent à la transduction du signal dépendant de H2O2 en tant que second messager, via leur état rédox. La suroxydation sous forme d’acide sulfinique des 2-Cys Prx typiques eucaryotes est une modification posttraductionnelle qui inactive l’activité peroxydase, permettant de réguler le passage du message cellulaire H2O2-dépendant. La réduction de cette espèce oxydée est essentielle pour la viabilité des cellules. Cette réaction est catalysée par les sulfirédoxines (Srx). Les études réalisées ont permis de caractériser le mécanisme catalytique de Srx de S. cerevisiae qui consiste en : 1) l’activation de la fonction acide sulfinique sous forme d’anhydride phosphoryl sulfinique, par transfert direct du phosphate ? de l’ATP ; 2) la réduction de la fonction acide sulfinique activée par attaque de la Cys catalytique de Srx, ce qui conduit à un intermédiaire covalent thiosulfinate Prx/Srx ; 3) le recyclage de Srx avec la libération de PrxSOH. Au niveau du recyclage de l’activité Srx, deux classes de Srx peuvent être définies, celle à deux Cys et celle à une Cys. La classe de Srx à deux Cys, composée jusqu’à présent de Srx de levures, possède une Cys de recyclage qui attaque le thiosulfinate au niveau de la Cys de Srx, libérant la PrxSOH et la Srx oxydée sous forme de pont disulfure intramoléculaire. Cette forme oxydée de Srx est ensuite reconnue et réduite par la thiorédoxine. La classe de Srx à une Cys dont font partie les Srx de mammifères, ne possédant pas de Cys de recyclage, passe par un mécanisme de recyclage impliquant un réducteur autre que la Trx, qui reduit directement la fonction thiosulfinate, et dont la nature reste à déterminer
Typical two-cysteine peroxiredoxines are involved in cell resistance against H2O2-induced oxidative stress, by reducing H2O2 in H2O. Furthermore, these enzymes take part in H2O2 signalling, which is transmitted and regulated by their redox state. The eukaryotic typical 2-Cys Prxs are subject to post-translational modification under sulfinic acid oxidation state, which inactivates have lost their peroxidase activity and thus regulates allows the passage of H2O2-dependent cellular message. Reduction of the sulfinic acid oxidation state is essential for the cell viability. Sulfiredoxin (Srx) catalyzes this reduction. These research studies demonstrated that the catalytic mechanism of Srx occurs in three steps: first, the sulfinic acid is activated as a sulfinyl phosphoryl anhydride intermediate by a direct transfer of the ?-phosphate of ATP; second, the activated sulfinic acid intermediate is reduced via attack of the catalytic Cys of Srx, which leads to formation of a thiosulfinate intermediate and; third Srx, is recycled with concomitant release of the PrxSOH product of the reaction. Two classes of Srx could be defined depending on the mechanism of Srx recycling. The class comprising yeast Srxs have one recycling Cys. This Cys attacks the thiosulfinate intermediate, resulting in PrxSOH release and formation of an oxidized Srx intermediate. This oxidized species, with an intramolecular disulfide bond, is recognized and reduced by thioredoxin. In the class comprising Srx devoid of recycling Cys, which includes the mammalian Srxs, Srx is recycled by a reducer distinct from thioredoxin, which reduces directly the thiosulfinate function
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Wozniak, Jocelyne. "Nouvelles méthodes pour la dégradation de la chaine latérale des acides biliaires." Paris 11, 1986. http://www.theses.fr/1986PA112291.

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Deux nouvelles méthodes de dégradations de la chaîne latérale des acides biliaires ont été élaborées. La première approche met en jeu une nouvelle voie de synthèse des Δ² -oxazolines ainsi que leur utilisation pour l'introduction d'une insaturation en position 22(23) sur la chaine latérale des acides biliaires. La généralité de ces deux réactions a été examinée. La deuxième voie est fondée sur une nouvelle synthèse des 23-céto esters à partir des acides biliaires. L'auto-oxydation de ces esters permet ensuite de dégrader la chaîne latérale. Un mécanisme pour cette dernière transformation a été proposé
Two new methods for the degradation of the side chain of bile acids have been elaborated. The first method involves a new synthetic pathway to Δ² -oxazolines and their use for the introduction of a double bond between carbon atoms 22 and 23. The general applicability to these two reactions has been examined. The second method is based on a novel synthesis of 23-keto esters derived from bile acids. Autoxidation of these esters leads ta subsequent side chain degradation. A mechanism for this degradation is proposed
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Coantic, Stéphanie. "Réactivité des N-sulfonyl, N-sulfinyl et N-sulfénylimines dans la réaction de Staudinger : la synthèse de β-lactames N-sulfurés et leur utilisation pour la synthèse de β-aminoacides [alpha]-oxygénés." Aix-Marseille 3, 2004. http://www.theses.fr/2004AIX30045.

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La synthèse des N-sulfonyl, des N-sulfinyl et des N-sulfénylimines a été réalisée. Ces imines N-sulfurées ont été testées dans la réaction de Staudinger sur des cétènes [alpha]-oxygénés. Cette réaction de cycloaddition [2+2] a été appliquée avec succès à de nombreuses imines N-sulfénylées pour donner des N-sulfényl β-lactames avec de bons rendements et de bonnes sélectivités. Ces azétidinones porteuses d'un groupement électrodonneur sur l'atome d'azote du cycle ont ensuite été engagées dans des réactions d'oxydation de l'atome de soufre pour donner de façon quantitative les produits N-sulfinylés et N-sulfonylés. Ces nouveaux β-lactames, porteurs de groupements électroattracteurs sur l'atome d'azote, ont été utilisés dans des réactions d'ouverture nucléophile avec des amines, des alcools ou des thiols pour donner de nouveaux β-aminoacides [alpha]-oxygénés
The synthesis of N-sulfonyl, N-sulfinyl and N-sulfenylimines has been achieved. These N-thiolated imines were tested in the Staudinger reaction with [alpha]-oxygenated ketenes. The [2+2] cycloaddition reaction was successfully applied to many N-sulfenylimines to give N-sulfenyl β-lactames with good yields and a good selectivity. These azetidinones bearing an electron-donor group on the nitrogen of the cycle were then used in the oxidation reaction of the sulphur to give the N-sulfinylated and N-sulfonylated cycloadducts. The new β-lactames bearing an electron-acceptor group on the nitrogen were used in nucleophilic ring opening reactions with amines, alcohols or thiols to give new [alpha]-oxygenated β-aminoacids
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Books on the topic "Sulfinic acids"

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Saul, Patai, ed. The chemistry of sulphinic acids, esters, and their derivatives. Chichester: Wiley, 1990.

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Mihail, Pacurar, and Krejci Gavril, eds. Garlic consumption and health. Hauppauge, NY: Nova Science Publishers, 2009.

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Reimer, Marie. The Addition Reactions of Sulphinic Acids. BiblioLife, 2009.

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Reimer, Marie. The Addition Reactions of Sulphinic Acids. BiblioBazaar, 2009.

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Isbell, R. Australian Soil Classification. CSIRO Publishing, 2016. http://dx.doi.org/10.1071/9781486304646.

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The Australian Soil Classification provides a framework for organising knowledge about Australian soils by allocating soils to classes via a key. Since its publication in 1996, this book has been widely adopted and formally endorsed as the official national system. It has provided a means of communication among scientists and land managers and has proven to be of particular value in land resource survey and research programs, environmental studies and education. Classification is a basic requirement of all science and needs to be periodically revised as knowledge increases. This Second Edition of The Australian Soil Classification includes updates from a working group of the National Committee on Soil and Terrain (NCST), especially in regards to new knowledge about acid sulfate soils (sulfidic materials). Modifications include expanding the classification to incorporate different kinds of sulfidic materials, the introduction of subaqueous soils as well as new Vertosol subgroups, new Hydrosol family criteria and the consistent use of the term reticulate. All soil orders except for Ferrosols and Sodosols are affected by the changes.
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Book chapters on the topic "Sulfinic acids"

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Peter, L. B. "Sulfinic Acids, Salts and Esters." In Inorganic Reactions and Methods, 19–20. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145197.ch24.

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van Roy, Frans, Volker Nimmrich, Anton Bespalov, Achim Möller, Hiromitsu Hara, Jacob P. Turowec, Nicole A. St. Denis, et al. "Cysteine Sulfinic Acid Reductase." In Encyclopedia of Signaling Molecules, 496. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0461-4_100330.

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Park, Seung Yong, Georgia Schuller-Levis, and Eunkyue Park. "A Novel Cysteine Sulfinic Acid Decarboxylase Knock-Out Mouse: Immune Function." In Taurine 9, 89–98. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15126-7_8.

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Baseggio Conrado, Alessia, Laura Pecci, Elisabetta Capuozzo, and Mario Fontana. "Oxidation of Hypotaurine and Cysteine Sulfinic Acid by Peroxidase-generated Reactive Species." In Taurine 9, 41–51. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15126-7_4.

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Park, Eunkyue, Seung Yong Park, In Soo Cho, Bo Sook Kim, and Georgia Schuller-Levis. "A Novel Cysteine Sulfinic Acid Decarboxylase Knock-Out Mouse: Immune Function (II)." In Advances in Experimental Medicine and Biology, 449–60. Dordrecht: Springer Netherlands, 2017. http://dx.doi.org/10.1007/978-94-024-1079-2_36.

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Park, Eunkyue, Seung Yong Park, Carl Dobkin, and Georgia Schuller-Levis. "A Novel Cysteine Sulfinic Acid Decarboxylase Knock-Out Mouse: Comparison Between Newborn and Weanling Mice." In Taurine 9, 3–16. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15126-7_1.

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de Souza, José João Lelis Leal, and Walter Antônio Pereira Abrahão. "Pyritic Subsoils in Acid Sulfate Soils and Similar Problems in Mined Areas with Sulfidic Rocks." In Subsoil Constraints for Crop Production, 109–23. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-00317-2_5.

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Gordon, Ronald, Seung Yong Park, Georgia Schuller-Levis, and Eunkyue Park. "A Novel Cysteine Sulfinic Acid Decarboxylase Knock-Out Mouse: Pathology of the Kidney and Lung in Newborn Pups." In Taurine 9, 17–28. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-15126-7_2.

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Park, Eunkyue, Seung Yong Park, In Soo Cho, Bo Sook Kim, and Georgia Schuller-Levis. "A Novel Cysteine Sulfinic Acid Decarboxylase Knock-Out Mouse: Taurine Distribution in Various Tissues With and Without Taurine Supplementation." In Advances in Experimental Medicine and Biology, 461–74. Dordrecht: Springer Netherlands, 2017. http://dx.doi.org/10.1007/978-94-024-1079-2_37.

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Wang, Wankun, Jinhui Peng, Zebiao Zhang, Lijuan Chu, and Guodong Lai. "A Kinetic Study of the Leaching of Germanium Dust and Fume by Sulfiiric Acid." In Supplemental Proceedings, 141–46. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118357002.ch19.

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Conference papers on the topic "Sulfinic acids"

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Helser, Jillian, Valérie Cappuyns, and Ana Lupu. "Acid generation potential and metal(loid) release from resuspended sulfidic mine waste." In Goldschmidt2021. France: European Association of Geochemistry, 2021. http://dx.doi.org/10.7185/gold2021.5205.

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Hadi, S., D. Asnawati, S. R. Kamali, Z. Zulkarnaen, S. Syaifuddin, and S. Hizmi. "Investigation of sulfidic natural water in Sebau Lombok Island to remove dissolved copper (Cu2+) in acid mine drainage." In PROCEEDINGS OF THE 3RD INTERNATIONAL SYMPOSIUM ON CURRENT PROGRESS IN MATHEMATICS AND SCIENCES 2017 (ISCPMS2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5064080.

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You might also be interested in the extended bibliographies on the topic 'Sulfinic acids' for particular source types:
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