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Journal articles on the topic 'Organosulfur'

Author: Grafiati

Published: 4 June 2021

Last updated: 31 October 2024

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1

Arisawa, Mieko, and Masahiko Yamaguchi. "Transition-metal-catalyzed synthesis of organosulfur compounds." Pure and Applied Chemistry 80, no. 5 (January 1, 2008): 993–1003. http://dx.doi.org/10.1351/pac200880050993.

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Rhodium complexes are efficient catalysts for the synthesis of organosulfur compounds. They catalyze the addition reaction of organosulfur groups to unsaturated compounds, the substitution of C-H with organosulfur groups, and single-bond metathesis reactions. They cleave S-S bonds and transfer the organosulfur groups to various organic and inorganic molecules, including alkynes, allenes, disulfides, sulfur, isonitriles, imines, diphosphines, thiophosphinites, hydrogen, 1-alkylthio-1-alkynes, thioesters, and allyl sulfides.

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2

Qiu, Yichen, Yunchao Feng, Ashley C. Lindsay, Xianhai Zeng, and Jonathan Sperry. "Synthesis of bio-based 2-thiothiophenes." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 379, no. 2209 (September 13, 2021): 20200350. http://dx.doi.org/10.1098/rsta.2020.0350.

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While the synthesis of bio-based compounds containing carbon, oxygen and (to a lesser extent) nitrogen is well studied, the production of organosulfur compounds from biomass has received virtually no attention, despite their widespread application throughout the chemical industry. Herein, we demonstrate that a range of bio-based 2-thiothiophenes are available from the biopolymer cellulose, proving that functionally diverse small-molecule organosulfurs can be prepared independent of fossil carbon. This article is part of the theme issue ‘Bio-derived and bioinspired sustainable advanced material

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3

Chauvin, Jean-Philippe R., Zosia A. M. Zielinski, and Derek A. Pratt. "Inspired by garlic: insights on the chemistry of sulfenic acids and the radical-trapping antioxidant activity of organosulfur compounds." Canadian Journal of Chemistry 94, no. 1 (January 2016): 1–8. http://dx.doi.org/10.1139/cjc-2015-0438.

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Organosulfur compounds have long been recognized as important antioxidants for the preservation of petroleum-derived products. It has also been suggested that the health benefits of garlic and related plant species can be ascribed to the radical-trapping antioxidant activity of some of their unique organosulfur constituents, such as allicin. This account highlights our efforts to elucidate the radical-trapping antioxidant mechanisms of allicin and related plant-derived organosulfur compounds as well as the organosulfur compounds used to preserve commercial and industrial products.

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4

Shine, Henry J. "Researches in organosulfur chemistry by a non-organosulfur chemist." Sulfur reports 15, no. 3 (August 1994): 381–93. http://dx.doi.org/10.1080/01961779408050635.

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5

Doddipatla, Srinivas, Chao He, Ralf I. Kaiser, Yuheng Luo, Rui Sun, Galiya R. Galimova, Alexander M. Mebel, and Tom J. Millar. "A chemical dynamics study on the gas phase formation of thioformaldehyde (H2CS) and its thiohydroxycarbene isomer (HCSH)." Proceedings of the National Academy of Sciences 117, no. 37 (August 28, 2020): 22712–19. http://dx.doi.org/10.1073/pnas.2004881117.

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Complex organosulfur molecules are ubiquitous in interstellar molecular clouds, but their fundamental formation mechanisms have remained largely elusive. These processes are of critical importance in initiating a series of elementary chemical reactions, leading eventually to organosulfur molecules—among them potential precursors to iron-sulfide grains and to astrobiologically important molecules, such as the amino acid cysteine. Here, we reveal through laboratory experiments, electronic-structure theory, quasi-classical trajectory studies, and astrochemical modeling that the organosulfur chemi

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6

Monika, Monika, Anita Dua, Sandeep Kumar, Sanjay Sharma, Sanjeev Gupta, and Ashwani Mittal. "Profiling of organosulfur compounds and amino acids in novel variety of Allium sativum (Hisar garlic 17) by HR-LCMS-QTOF." Journal of Applied and Natural Science 16, no. 1 (March 20, 2024): 315–24. http://dx.doi.org/10.31018/jans.v16i1.5386.

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Over the past few years, the biological properties of garlic have been utilized as an attractive natural alternative to many therapeutic drugs. The biological effects of garlic have been ascribed to organosulfur compounds, secondary metabolites derived from amino acids. The present study aimed to investigate the extracts of a novel garlic variety (Hisar garlic 17) after processing it as fresh, dry, heated, and aged in different solvents and then analyzed with highly sensitive and rapid technique i.e., High resolution liquid chromatograph mass spectrometer quadrupole time of flight (HR-LCMS-QTO

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7

Arisawa, Mieko, and Masahiko Yamaguchi. "Rhodium-Catalyzed Synthesis of Organosulfur Compounds Involving S-S Bond Cleavage of Disulfides and Sulfur." Molecules 25, no. 16 (August 7, 2020): 3595. http://dx.doi.org/10.3390/molecules25163595.

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Organosulfur compounds are widely used for the manufacture of drugs and materials, and their synthesis in general conventionally employs nucleophilic substitution reactions of thiolate anions formed from thiols and bases. To synthesize advanced functional organosulfur compounds, development of novel synthetic methods is an important task. We have been studying the synthesis of organosulfur compounds by transition-metal catalysis using disulfides and sulfur, which are easier to handle and less odiferous than thiols. In this article, we describe our development that rhodium complexes efficiently

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8

Islam, Fawad, and Qingle Zeng. "Advances in Organosulfur-Based Polymers for Drug Delivery Systems." Polymers 16, no. 9 (April 25, 2024): 1207. http://dx.doi.org/10.3390/polym16091207.

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Organosulfur-based polymers have unique properties that make them useful for targeted and managed drug delivery, which can improve therapy while reducing side effects. This work aims to provide a brief review of the synthesis strategies, characterization techniques, and packages of organosulfur-based polymers in drug delivery. More importantly, this work discusses the characterization, biocompatibility, controlled release, nanotechnology, and targeted therapeutic aspects of these important structural units. This review provides not only a good comprehension of organosulfur-based polymers but a

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9

Egbujor, Melford Chuka, Maria Petrosino, Karim Zuhra, and Luciano Saso. "The Role of Organosulfur Compounds as Nrf2 Activators and Their Antioxidant Effects." Antioxidants 11, no. 7 (June 26, 2022): 1255. http://dx.doi.org/10.3390/antiox11071255.

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Nuclear factor erythroid 2-related factor 2 (Nrf2) signaling has become a key pathway for cellular regulation against oxidative stress and inflammation, and therefore an attractive therapeutic target. Several organosulfur compounds are reportedly activators of the Nrf2 pathway. Organosulfur compounds constitute an important class of therapeutic agents in medicinal chemistry due to their ability to participate in biosynthesis, metabolism, cellular functions, and protection of cells from oxidative damage. Sulfur has distinctive chemical properties such as a large number of oxidation states and v

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10

Yuen, Pong Kau, and Cheng Man Diana Lau. "New approach for assigning mean oxidation number of carbons to organonitrogen and organosulfur compounds." Chemistry Teacher International 4, no. 1 (October 8, 2021): 1–13. http://dx.doi.org/10.1515/cti-2021-0015.

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Abstract Organonitrogen and organosulfur compounds are abundant in the natural environment. To understand the biological redox pathways properly, it is important for learners to be able to count the oxidation number of organic carbons. However, the process of counting is not always easy. In addition, organonitrogen and organosulfur molecules are seldom studied. To compensate these problems, this paper explores the bond-dividing method, which can effectively determine the mean oxidation number of carbons of organonitrogen and organosulfur molecules. This method uses the cleavage of carbon-sulfu

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11

Chou, Liang Hsiung. "On Improvements of Rubberized Concrete with Organosulfur Compounds." Advanced Materials Research 156-157 (October 2010): 1459–62. http://dx.doi.org/10.4028/www.scientific.net/amr.156-157.1459.

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Crumb rubbers have been investigated as additives to concrete and promising results have been observed. Organosulfur compounds from a petroleum-refining factory were used to modify the surface properties of crumb rubbers. The intermolecular interaction forces between cement hydration products (C-S-H) and rubber crumbs were measured directly by an atomic force microscope (AFM) equipped with a colloid probe. Experimental data indicate that crumb rubber surface is more hydrophilic after the treatment with organosulfur compounds and the intermolecular interaction forces between C-S-H and rubber in

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12

Nakahodo, Tsukasa, Midori O. Ishitsuka, Yuta Takano, Takahiro Tsuchiya, Takeshi Akasaka, M. Angeles Herranz, Nazario Martin, Dirk M. Guldi, and Shigeru Nagase. "Organosulfur-Based Fullerene Materials." Phosphorus, Sulfur, and Silicon and the Related Elements 186, no. 5 (May 1, 2011): 1308–11. http://dx.doi.org/10.1080/10426507.2010.523033.

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13

Kiełbasiński, Piotr. "Biocatalysis in Organosulfur Chemistry." Phosphorus, Sulfur, and Silicon and the Related Elements 186, no. 5 (May 1, 2011): 1104–18. http://dx.doi.org/10.1080/10426507.2010.541397.

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14

Weil, Edward D. "RECENT INDUSTRIAL ORGANOSULFUR CHEMISTRY." Phosphorus, Sulfur, and Silicon and the Related Elements 59, no. 1-4 (May 1991): 31–46. http://dx.doi.org/10.1080/10426509108045699.

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15

Uehara, Kazuhiro, and Katsuhiko Tomooka. "Planar Chiral Organosulfur Cycles." Chemistry Letters 38, no. 11 (November 5, 2009): 1028–29. http://dx.doi.org/10.1246/cl.2009.1028.

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16

ITO, OSAMU. "Reactivities of organosulfur radicals." NIPPON GOMU KYOKAISHI 61, no. 3 (1988): 201–8. http://dx.doi.org/10.2324/gomu.61.201.

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17

Tarbell, D. S. "Researches on Organosulfur Compounds." Sulfur reports 6, no. 1 (September 1986): 1–11. http://dx.doi.org/10.1080/01961778608082489.

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18

Douglass, Irwin B., and Miriam L. Douglass. "Adventures in Organosulfur Chemistry." Sulfur reports 17, no. 1 (October 1995): 129–53. http://dx.doi.org/10.1080/01961779508047887.

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19

Doraghi, Fatemeh, Seyedeh Pegah Aledavoud, Mehdi Ghanbarlou, Bagher Larijani, and Mohammad Mahdavi. "N-Sulfenylsuccinimide/phthalimide: an alternative sulfenylating reagent in organic transformations." Beilstein Journal of Organic Chemistry 19 (September 27, 2023): 1471–502. http://dx.doi.org/10.3762/bjoc.19.106.

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In the field of organosulfur chemistry, sulfenylating agents are an important key in C–S bond formation strategies. Among various organosulfur precursors, N-sulfenylsuccinimide/phthalimide derivatives have shown highly electrophilic reactivity for the asymmetric synthesis of many organic compounds. Hence, in this review article, we focus on the application of these alternative sulfenylating reagents in organic transformations.

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20

Rickly, Pamela S., Hongyu Guo, Pedro Campuzano-Jost, Jose L. Jimenez, Glenn M. Wolfe, Ryan Bennett, Ilann Bourgeois, et al. "Emission factors and evolution of SO₂ measured from biomass burning in wildfires and agricultural fires." Atmospheric Chemistry and Physics 22, no. 23 (December 13, 2022): 15603–20. http://dx.doi.org/10.5194/acp-22-15603-2022.

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Abstract. Fires emit sufficient sulfur to affect local and regional air quality and climate. This study analyzes SO2 emission factors and variability in smoke plumes from US wildfires and agricultural fires, as well as their relationship to sulfate and hydroxymethanesulfonate (HMS) formation. Observed SO2 emission factors for various fuel types show good agreement with the latest reviews of biomass burning emission factors, producing an emission factor range of 0.47–1.2 g SO2 kg−1 C. These emission factors vary with geographic location in a way that suggests that deposition of coal burning emi

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21

Praveen, Reddy P., and Rao V. Uma Maheswara. "Effect of nutrient and physical parameters on dibenzothiophene desulfurization activity of Streptomyces sp. VUR PPR 101 isolated from oil contaminated soils of mechanical workshops." Research Journal of Chemistry and Environment 26, no. 6 (May 25, 2022): 86–99. http://dx.doi.org/10.25303/2606rjce086099.

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Motor vehicles use petroleum products and release sulfur dioxide gas which causes deleterious effects to environment and humans. The sulfur containing compounds present in petroleum products especially organosulfur compounds serve as major source of sulfur dioxide emission. During refining process, petroleum products are subjected to hydrodesulfurization for the removal of sulfur, which is not an efficient method and most of the organosulfur compounds are not eliminated particularly dibenzothiophene and its derivatives. A process known as biodesulfurization which employs microorganisms was sug

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22

Reed, Nathan W., Randall L. Shearer, Shawn Erin McGlynn, Boswell A. Wing, Margaret A. Tolbert, and Eleanor C. Browne. "Abiotic Production of Dimethyl Sulfide, Carbonyl Sulfide, and Other Organosulfur Gases via Photochemistry: Implications for Biosignatures and Metabolic Potential." Astrophysical Journal Letters 973, no. 2 (September 23, 2024): L38. http://dx.doi.org/10.3847/2041-8213/ad74da.

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Abstract Among the atmospheric gases that have been proposed as possible biosignatures in exoplanetary atmospheres, organosulfur gases are currently considered one of the more robust indicators of extant life. These gases include dimethyl sulfide (DMS; CH3SCH3), carbonyl sulfide (OCS), and carbon disulfide (CS2), which are predominantly secondary metabolic products of living organisms on Earth. Here we present results that challenge this interpretation and provide constraints on the robustness of organosulfur gases as biosignatures. Through laboratory photochemical experiments, we show the abi

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23

Kropp, Kevin G., and Phillip M. Fedorak. "A review of the occurrence, toxicity,and biodegradation of condensed thiophenes found in petroleum." Canadian Journal of Microbiology 44, no. 7 (July 1, 1998): 605–22. http://dx.doi.org/10.1139/w98-045.

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Condensed thiophenes comprise a significant portion of the organosulfur compounds in petroleum and in other products from fossil fuels. Dibenzothiophene (DBT) has served as a model compound in biodegradation studies for over two decades. However, until quite recently, few other organosulfur compounds were studied, and their fates in petroleum-contaminated environments are largely unknown. This paper presents a review of the types of organosulfur compounds found in petroleum and summarizes the scant literature on toxicity studies with condensed thiophenes. Reports on the biodegradation of benzo

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24

Yoshioka, Yuri, Shinichi Matsumura, and Masanori Morimoto. "Deodorant Activity of Black Cumin Seed Essential Oil against Garlic Organosulfur Compound." Biomolecules 11, no. 12 (December 14, 2021): 1874. http://dx.doi.org/10.3390/biom11121874.

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The deodorant activity of black cumin (Nigella sativa L.) seed, a spice used to flavor curry and vegetable foods in Southwest Asia, against garlic (Allium sativum L.) organosulfur compounds related to human malodor was evaluated. Black cumin seed essential oil showed remarkable deodorant activity against garlic essential oil. The mode of action of this deodorant activity was presumed to be that black cumin seed essential oil covalently reacted with the organosulfur compounds in garlic. Therefore, thymoquinone, which is a major constituent in black cumin seed essential oil, and allyl mercaptan,

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25

Robert M. Moriarty, Rajesh Naithani, and Bhushan Surve. "Organosulfur Compounds in Cancer Chemoprevention." Mini-Reviews in Medicinal Chemistry 7, no. 8 (August 1, 2007): 827–38. http://dx.doi.org/10.2174/138955707781387939.

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26

Firouzabadi, Habib, and Arezu Jamalian. "Reduction of oxygenated organosulfur compounds." Journal of Sulfur Chemistry 29, no. 1 (January 22, 2008): 53–97. http://dx.doi.org/10.1080/17415990701684776.

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27

Pope, John M., Toshitada Sato, Eiichi Shoji, Noboru Oyama, Kevin C. White, and Daniel A. Buttry. "Organosulfur/Conducting Polymer Composite Cathodes." Journal of The Electrochemical Society 149, no. 7 (2002): A939. http://dx.doi.org/10.1149/1.1482768.

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28

Takeda, Takeshi, Yasuo Horikawa, Tadahiro Nomura, Mikako Watanabe, Ichiro Miura, and Tooru Fujiwara. "Desulfurizative Titanation of Organosulfur Compounds." Phosphorus, Sulfur, and Silicon and the Related Elements 120, no. 1 (January 1, 1997): 391–92. http://dx.doi.org/10.1080/10426509708545563.

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29

Vazquez-Prieto, Marcela A., and Roberto M. Miatello. "Organosulfur compounds and cardiovascular disease." Molecular Aspects of Medicine 31, no. 6 (December 2010): 540–45. http://dx.doi.org/10.1016/j.mam.2010.09.009.

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30

Eckert-Maksic, Mirjana, and Davor Margetic. "Ionic hydrogenation of organosulfur compounds." Energy & Fuels 5, no. 2 (March 1991): 327–32. http://dx.doi.org/10.1021/ef00026a018.

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31

Crank, George, and Achmad Mursyidi. "Photochemistry of some organosulfur pesticides." Journal of Photochemistry and Photobiology A: Chemistry 68, no. 3 (September 1992): 289–97. http://dx.doi.org/10.1016/1010-6030(92)85238-p.

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32

Harpp, David N., John Robertson, Kim Laycock, and David Butler. "Organosulfur Antioxidants in Hydrocarbon Oils." Sulfur reports 4, no. 6 (July 1985): 195–219. http://dx.doi.org/10.1080/01961778508082477.

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33

Truce, William E. "Forty Years in Organosulfur Chemistry." Sulfur reports 9, no. 4 (January 1990): 351–57. http://dx.doi.org/10.1080/01961779008048733.

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34

Kulich, Donald M., and J. Reid Shelton. "Organosulfur antioxidants: Mechanisms of action." Polymer Degradation and Stability 33, no. 3 (January 1991): 397–410. http://dx.doi.org/10.1016/0141-3910(91)90085-6.

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35

Subroto, E., Y. Cahyana, Tensiska, Mahani, F. Filianty, E. Lembong, E. Wulandari, D. Kurniati, R. A. Saputra, and F. Faturachman. "Bioactive compounds in garlic (Allium sativum L.) as a source of antioxidants and its potential to improve the immune system: a review." Food Research 5, no. 6 (November 7, 2021): 1–11. http://dx.doi.org/10.26656/fr.2017.5(6).042.

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Garlic (Allium sativum L.) is a type of spice derived from layered tubers, widely used as a source of flavour, taste, and cooking spices. Garlic is a therapeutic ingredient rich in bioactive compounds and antioxidants. The purpose of compiling this review is to provide information about bioactive compounds in garlic as a source of bioactive compounds and their potential to improve the immune system. This review also discussed the various effects of garlic processing on the stability and activity of bioactive compounds and the changes that occur during storage. Garlic contains high levels of or

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36

Avgeri, Ioanna, Konstantina Zeliou, Spyridon A. Petropoulos, Penelope J. Bebeli, Vasileios Papasotiropoulos, and Fotini N. Lamari. "Variability in Bulb Organosulfur Compounds, Sugars, Phenolics, and Pyruvate among Greek Garlic Genotypes: Association with Antioxidant Properties." Antioxidants 9, no. 10 (October 9, 2020): 967. http://dx.doi.org/10.3390/antiox9100967.

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In order to assess the diversity of Greek garlic (Allium sativum L.) landraces, 34 genotypes including commercial ones were grown in the same field and their content in organosulfur compounds, pyruvate, total sugars, and total phenolics, alongside antioxidant capacity, was determined. The organosulfur compounds were studied by Gas Chromatography–Mass Spectrometry (GC–MS) after ultrasound-assisted extraction in ethyl acetate, identifying 2-vinyl-4H-1,3-dithiin and 3-vinyl-4H-1,2-dithiin as the predominant compounds, albeit in different ratios among genotypes. The bioactivity and the polar metab

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37

Dewi, Ardhia Deasy Rosita, Joni Kusnadi, and Wen-Ling Shih. "Comparison of the Main Bioactive Compounds and Antioxidant Activity from Garlic Water-soluble and Garlic Oil." KnE Life Sciences 3, no. 5 (September 11, 2017): 20. http://dx.doi.org/10.18502/kls.v3i5.975.

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<p class="Els-Abstract-text">Garlic is a natural source which has abundant organosulfur constituents. Garlic is divided into water-soluble organosulfur constituents mainly SAC (S-allylcystein), NAC (N-acetylcysteine) and oil soluble organosulfur constituents such as DATS (diallyl trisulfide), DADS (diallyl disulfide), DAS (diallyl sulfide). The aim of this research was to compare the bioactive constituents and antioxidant activity between garlic water-soluble and garlic oil. Garlic water-soluble constituents were identified by Liquid Chromatography–Mass Spectrometry (LC-MS) and five cons

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38

Tang, Shuai, Qiliang Chen, Yubing Si, Wei Guo, Bingwei Mao, and Yongzhu Fu. "Size Effect of Organosulfur and In Situ Formed Oligomers Enables High‐Utilization Na–Organosulfur Batteries." Advanced Materials 33, no. 33 (July 11, 2021): 2100824. http://dx.doi.org/10.1002/adma.202100824.

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39

Kopelberg, M., I. L. Goldman, J. E. P. Debaene, and B. S. Schwartz. "Antiplatelet Activity is Positively Correlated with Pungency and Solids in Onion (Allium cepa L.)." HortScience 30, no. 4 (July 1995): 769A—769. http://dx.doi.org/10.21273/hortsci.30.4.769a.

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Onion (Allium cepa L.) and other vegetable Alliums have long been recognized for the antiplatelet properties. Consumers may benefit from the medicinal value of onions because they are commonly eaten raw in salads and the antiplatelet factor is destroyed by heat. Recent work indicates antiplatelet activity in Allium sp. may be due to the presence of native organosulfur compounds. The concentration of organosulfur compounds correlates positively with pungency, varies with onion cultivar, and is influenced by environmental factors. Bulb dry matter content, or solids, is positively correlated with

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40

Debaene, Jan E. P., and I. L. Goldman. "Environmental Effects and Postharvest Flux of Antiplatelet Activity, Pungency, and Solids in Onion (Allium cepa)." HortScience 32, no. 3 (June 1997): 543D—543. http://dx.doi.org/10.21273/hortsci.32.3.543d.

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Onion is a species within the Allium genus with great culinary importance. Onion extract contains organosulfur compounds that influence pungency and inhibit blood platelet aggregation. Antiplatelet activity has the potential of reducing cardiovascular disease. Onions are typically held in postharvest storage for up to 160 days, during which time volatile organosulfur compounds may be affected. A study was conducted to evaluate antiplatelet activity, pungency, and percent solids during cold storage of onions grown in replicated plots in Wisconsin and Oregon in 1994 and 1995. Organosulfur compou

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41

Ahmad, Abrar, Othman A. Baothman, Muhammad Shahid Nadeem, and Varish Ahmad. "Biodesulfurizing Microbes in the Petroleum Refinery Areas of Saudi Arabia." Journal of Pure and Applied Microbiology 17, no. 3 (September 1, 2023): 1737–47. http://dx.doi.org/10.22207/jpam.17.3.39.

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Gordonia sp., Rhodococcus, Paenibaccilus, Mycobacterium and many other desulfurizing strains have shown good potential for dibenzothiophene (DBT), 4, 6-Dimethyldibenzothiophene (4-6-Dimethyl dibenzothiophene) and other organosulfur biodesulfurization. These are microbes which have 4S pathway to remove S from remaining calcitarant organosulfur compounds even after deep desulfurization. Sulfur compounds present in crude oils, diesel and petrol when combust in engines they emerge out in the form of elemental Sulfur, which causes environmental and health problems. Therefore, efforts are going to r

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42

Zhang, Danna, Guochun Lv, Xiaomin Sun, Chenxi Zhang, and Zhiqiang Li. "A theoretical study on the formation and oxidation mechanism of hydroxyalkylsulfonate in the atmospheric aqueous phase." RSC Advances 9, no. 47 (2019): 27334–40. http://dx.doi.org/10.1039/c9ra05193g.

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43

Al-Khazaali, Wisam Mohammed Kareem, and Seyed Ahmad Ataei. "Biochemical Analytical Methods of Fossil Fuels Biodesulfurization Treatment." IOP Conference Series: Earth and Environmental Science 1223, no. 1 (August 1, 2023): 012012. http://dx.doi.org/10.1088/1755-1315/1223/1/012012.

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Abstract Biodesulfurization of fossil fuels is a promising method for treating the high sulfur content of crude oils and their derivatives in the future. This method is environmentally friendly and can desulfurize recalcitrant organosulfur compounds. Bioreactions depend on the treated fluid, targeted sulfur compounds, and the biotreaters applied. Various analytical methods support this treatment, including measurement of total sulfur and speciation of organosulfur compounds (HCS). Monitoring of intermediates, end products, biomass growth, and identification using methods such as genes, DNA, an

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44

Park, Kyung-Ran, Ji-Youn Kim, Jin Tae Hong, and Hyung-Mun Yun. "A novel organosulfur compound, thiacremonone, regulates RANKL-induced osteoclast differentiation." RSC Advances 7, no. 49 (2017): 30657–62. http://dx.doi.org/10.1039/c7ra02049j.

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45

Wang, Ming, and Xuefeng Jiang. "Prospects and Challenges in Organosulfur Chemistry." ACS Sustainable Chemistry & Engineering 10, no. 2 (January 3, 2022): 671–77. http://dx.doi.org/10.1021/acssuschemeng.1c07636.

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46

Voss, Jürgen. "History of nineteenth-century organosulfur chemistry." Journal of Sulfur Chemistry 30, no. 2 (April 1, 2009): 167–207. http://dx.doi.org/10.1080/17415990802673017.

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47

Aggarwal, Varinder K. "Book Review, Organosulfur Chemistry: Synthetic Aspects." Synthesis 1996, no. 06 (June 1996): 790–92. http://dx.doi.org/10.1055/s-1996-4275.

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Block, Eric. "The Organosulfur Chemistry of the Onion." Phosphorus, Sulfur, and Silicon and the Related Elements 58, no. 1-4 (April 1991): 3–15. http://dx.doi.org/10.1080/10426509108040623.

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Posner, G. H. "New synthetic methodology using organosulfur compounds." Pure and Applied Chemistry 62, no. 10 (January 1, 1990): 1949–56. http://dx.doi.org/10.1351/pac199062101949.

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Okazaki, Renji, and Kei Goto. "Synthesis of highly reactive organosulfur compounds." Heteroatom Chemistry 13, no. 5 (2002): 414–18. http://dx.doi.org/10.1002/hc.10068.

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