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Journal articles on the topic 'Alkylthio'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Barlin, GB, and SJ Ireland. "Imidazo[1,2-B]pyridazines. II. 6-Alkylthio and 6-Arylthio-3-methoxy-2-phenylimidazo[1,2-b]pyridazines." Australian Journal of Chemistry 40, no. 8 (1987): 1491. http://dx.doi.org/10.1071/ch9871491.

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A series of 6-alkylthio- and 6-arylthio-3-methoxy-2-phenylimidazo[l,2- b]pyridazines has been prepared from 6-alkylthio-and 6-arylthio-pyridazin-3-amines through the corresponding 6-alkylthio-and 6-arylthio-2-phenylimidazo[l,2-b] pyridazin-3(5H)-ones.

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2

Amiel, Pascale, Abdallah Mahamoud, Pierre Brouant, et al. "Tautomérie du 2,5-dimercapto-1,3,4-thiadiazole et synthèse de thiadiazoloacridiniques." Canadian Journal of Chemistry 73, no. 8 (1995): 1258–66. http://dx.doi.org/10.1139/v95-154.

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Some 2(3H)-thione-5-alkylthio-1,3,4-thiadiazoles were prepared with a view to arylating these compounds with 9-chloroacridines. Using pyridine as solvent and base, this arylation led to the 2-thione-(N)3-acridinyl-5-alkylthio-1,3,4-thiadiazoles. Molecular structures of the latter were determined either by NMR spectroscopy or by referring to X-ray crystallography of the 5-(diethylaminoethylthio)-1,3,4-thiadiazole-2-thione. Thus, with respect to the tautomeric equilibrium of the compound investigated, the thione group was detected either in the solid state or in solution. In contrast, 2-acridiny

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3

Arakawa, Yuki, Yuko Ishida, Yukito Sasaki, Shunsuke Sasaki, Masatoshi Tokita, and Hideto Tsuji. "Alkylthio-based asymmetric liquid crystals: unravelling the substituent effects and intercalated cybotactic nematic and smectic phases." Materials Advances 3, no. 7 (2022): 3218–28. http://dx.doi.org/10.1039/d2ma00050d.

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A homologous series of alkylthio- and alkoxy-based asymmetric calamitic liquid crystal (LC) molecules was developed. The effects of alkylthio groups on the phase transition properties and unexpected intercalated LC phase structures were studied.

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4

Katritzky, Alan R., Herman H. Odens, Michael V. Voronkov, Charles J. Rostek, and Otto W. Maender. "Rubber Chemicals Derived from Conjugate Addition. II. Synthesis of a Novel Class of Benzoquinone Diimines." Rubber Chemistry and Technology 74, no. 5 (2001): 927–45. http://dx.doi.org/10.5254/1.3547662.

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Abstract Various 2-alkylthio-5-amino- and 2,5-diamino-1,4-phenylenediamines were prepared by treatment of N-(1,3-dimethylbutyl)- N′-phenyl-1,4-quinonediimine with thiols and amines using air as an oxidizing agent. Key 2-alkylthio-1, 4-benzoquinone diimines were prepared via Ag2O oxidation of the corresponding 1,4-phenylenediamines.

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5

Khrapova, Ekaterina A., Natalya A. Ryzhkova, Victor V. Dotsenko, and Nicolai A. Aksenov. "The Aminometylation of 4-(Alkylthio)-6-amino-2-oxo(thioxo)-1,2-dihydropyridine-3,5-dicarbonitriles." Chemistry Proceedings 3, no. 1 (2020): 30. http://dx.doi.org/10.3390/ecsoc-24-08401.

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Easily available 2-(bis(alkylthio)methylene)malononitriles react with cyanoacetamide or cyanothioacetamide to give 4-(alkylthio)-6-amino-2-oxo(thioxo)-1,2-dihydropyridine-3,5-dicarbonitriles. Upon treatment with primary amines and/or HCHO, the compounds undergo heterocyclization to afford new pyrido[1,2-a][1,3,5]triazines or ring-condensed 1,3,5,7-tetrazocine derivatives.

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6

Oshita, Hiromi, та Yuichi Shimazaki. "π–π Stacking Interaction of Metal Phenoxyl Radical Complexes". Molecules 27, № 3 (2022): 1135. http://dx.doi.org/10.3390/molecules27031135.

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π–π stacking interaction is well-known to be one of the weak interactions. Its importance in the stabilization of protein structures and functionalization has been reported for various systems. We have focused on a single copper oxidase, galactose oxidase, which has the π–π stacking interaction of the alkylthio-substituted phenoxyl radical with the indole ring of the proximal tryptophan residue and catalyzes primary alcohol oxidation to give the corresponding aldehyde. This stacking interaction has been considered to stabilize the alkylthio-phenoxyl radical, but further details of the interact

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7

Safonov, A. A., and O. I. Panasenko. "Synthesis, antimicrobial and antifungal activity of 3-(2-bromophenyl)-5-(alkylthio)-4-phenyl-4H-1,2,4-triazoles." Current issues in pharmacy and medicine: science and practice 15, no. 3 (2022): 235–40. http://dx.doi.org/10.14739/2409-2932.2022.3.264691.

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To select a molecule that could become a promising pharmacological agent, chemists use already-known heterocyclic bases by adding pharmacologically active groups. One such heterocyclic system is 1,2,4-triazole base, on the basis of which a huge number of biologically active compounds have already been found. It is known that 1,2,4-triazole derivatives show a fairly high antimicrobial and antifungal effect while remaining low-toxic compounds and 5-alkylthio-1,2,4-triazoles exhibit antimicrobial and antifungal activity. Based on the literature search, it can be concluded that 3-(2-bromophenyl)-5

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8

Kráľová, Katarína, František Šeršeň, Věra Klimešová, and Karel Waisser. "Effect of 2-Alkylthio-4-pyridinecarbothiamides on Photosynthetic Electron Transport in Spinach Chloroplasts." Collection of Czechoslovak Chemical Communications 62, no. 3 (1997): 516–20. http://dx.doi.org/10.1135/cccc19970516.

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2-Alkylthio-4-pyridinecarbothiamides (1) inhibit photosynthetic electron transport in spinach chloroplasts. The dependence of photosynthesis-inhibiting activity upon the lipophilicity of 2-alkylthio substituent shows quasi-parabolic course with maximum effectiveness at 2-octyl derivative. The site of action of 1 is the intermediate D+, corresponding to tyrosine radical, which is situated in D2 protein on the donor side of photosystem 2.

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9

Kreher, Richard P., Udo Feldhoff, and Frank Jelitto. "Untersuchungen zur Chemie von Isoindolen und Isoindoleninen, XXXII [1] Elektrophile Substitutionsreaktionen von 2-Aryl-2H-isoindolen mit Trifluoressigsäureanhydrid / Studies on the Chemistry of Isoindoles and Isoindolenines, XXXII [1] Electrophilic Substitution Reactions of 2-Aryl-2H-isoindoles with Trifluoroacetic Anhydride." Zeitschrift für Naturforschung B 43, no. 10 (1988): 1332–40. http://dx.doi.org/10.1515/znb-1988-1020.

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The reaction of 2-aryl-2H-isoindoles with trifluoroacetic anhydride in pyridine leads to the formation of the corresponding 1-trifluoroacetyl-2-aryl-2H-isoindoles with acceptable yields. 1-Alkylthio-2-aryl-2H-isoindoles can be generated from 3-alkylthio-2-aryl-1 H-isoindolium-tri-fluoromethanesulfonates with pyridine and acylated in the same manner. Protonation occurs at 1-position and yields isolable 1H-isoindolium salts.

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10

Ranken, Paul F., and B. Gary McKinnie. "Alkylthio aromatic amines." Journal of Organic Chemistry 54, no. 12 (1989): 2985–88. http://dx.doi.org/10.1021/jo00273a044.

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11

Kittivarapong, Sirichai, Chachanat Thebtaranonth, and Yodhathai Thebtaranonth. "Synthesis of 2-Alkylthio-3-chloro- and 2,3-Bis(alkylthio)propanals." Synthesis 1990, no. 10 (1990): 883–84. http://dx.doi.org/10.1055/s-1990-27041.

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12

Yang, Yanou, Feng Qiu, Jonathan L. Josephs, W. Griffith Humphreys, and Yue-Zhong Shu. "Bioactivation of 2-(Alkylthio)-1,3,4-Thiadiazoles and 2-(Alkylthio)-1,3-Benzothiazoles." Chemical Research in Toxicology 25, no. 12 (2012): 2770–79. http://dx.doi.org/10.1021/tx3003998.

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13

Khan, Zafar, and Tony Durst. "Preparation of 1-thio and 1-amino substituted 1,3-dihydrobenzo[c]thiophene 2,2-dioxides." Canadian Journal of Chemistry 65, no. 3 (1987): 482–86. http://dx.doi.org/10.1139/v87-083.

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The 1-hydroxy substituent in 1-hydroxy-1,3-dihydrobenzo[c]thiophene 2,2-dioxides is readily replaced by alkoxy, alkylthio, and amino groups. These compounds serve as precursors of alkoxy, alkylthio, and amino substituted o-quinodimethanes. Cycloaddition reactions between a series of 1,4-disubstituted o-quinodimethanes bearing a phenyl group and one of the above heteroatoms, and typical dienophiles such as dimethyl fumarate and methyl crotonate were carried out. The phenyl group controlled both the regiochemistry and stereochemistry of these cycloaddition reactions, with the major products bein

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14

Zhao, Mingzhi, Zi Qiao, Xiaofeng Chen, et al. "High photovoltaic performance of as-cast devices based on new quinoxaline-based donor–acceptor copolymers." Polymer Chemistry 8, no. 37 (2017): 5688–97. http://dx.doi.org/10.1039/c7py01060e.

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15

Gompper, R., and R. Guggenberger. "Alkylthio-substituted (aza)fulvalenes." Tetrahedron 42, no. 3 (1986): 839–48. http://dx.doi.org/10.1016/s0040-4020(01)87490-1.

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16

Wu, Yue, Xiao Cheng, Guiying Xu, Yaowen Li, Chaohua Cui, and Yongfang Li. "Manipulating the photovoltaic properties of small-molecule donor materials by tailoring end-capped alkylthio substitution." RSC Advances 6, no. 110 (2016): 108908–16. http://dx.doi.org/10.1039/c6ra23898j.

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17

Kesavan, Arunachalam, and Pazhamalai Anbarasan. "Catalytic enantioselective oxysulfenylation of o-vinylanilides." Chemical Communications 58, no. 2 (2022): 282–85. http://dx.doi.org/10.1039/d1cc05835e.

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18

Arakawa, Yuki, Yukito Sasaki, Kazunobu Igawa, and Hideto Tsuji. "Hydrogen bonding liquid crystalline benzoic acids with alkylthio groups: phase transition behavior and insights into the cybotactic nematic phase." New Journal of Chemistry 41, no. 14 (2017): 6514–22. http://dx.doi.org/10.1039/c7nj00282c.

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19

Li, Bin, Qilin Zhang, Gaole Dai, et al. "Understanding the impact of side-chains on photovoltaic performance in efficient all-polymer solar cells." Journal of Materials Chemistry C 7, no. 40 (2019): 12641–49. http://dx.doi.org/10.1039/c9tc02141h.

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20

Cheung, Andy Man Hong, Han Yu, Siwei Luo, et al. "Incorporation of alkylthio side chains on benzothiadiazole-based non-fullerene acceptors enables high-performance organic solar cells with over 16% efficiency." Journal of Materials Chemistry A 8, no. 44 (2020): 23239–47. http://dx.doi.org/10.1039/d0ta08830g.

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21

Dovbnya, Dmytro V., Andrii G. Kaplaushenko, and Alla S. Korzhova. "Synthesis and alkylation of 5-aryl-1,2-dihydro-3H-1,2,4-triazole-3-thiones." Journal of Organic and Pharmaceutical Chemistry 19, no. 2(74) (2021): 53–59. http://dx.doi.org/10.24959/ophcj.21.188135.

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5-R-1,2,4-triazole-3-thiones and their derivatives are easy to obtain; they have low toxicity and a broad spectrum of the biological activity. It makes this class of heterocyclic compounds promising for creating potential drugs. Aim. To develop the preparative methods for the synthesis of 5-aryl-1,2-dihydro-3H-1,2,4-triazole-3-thiones and study their reactivity in the alkylation reaction. Results and discussion. New 5-aryl-1,2-dihydro-3H-1,2,4-triazole-3-thiones were synthesized. The latter were used for the synthesis of 3-aryl-5-(alkylthio)-4H-1,2,4-triazoles. Experimental part. Using a serie

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22

Lee, Seung-Hoon, Bogyu Lim, Mingyuan Pei, Hoichang Yang та Yong-Young Noh. "Highly π-extended small molecules with bis(alkylthio)methylene side chains for organic field-effect transistors". Journal of Materials Chemistry C 6, № 28 (2018): 7604–11. http://dx.doi.org/10.1039/c8tc01852a.

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This paper reports on indacenodithiophene (IDT) based conjugated small molecules with rarely investigated side chain of bis(alkylthio)methylene as dimethyloctyl (SMOIC) and ethylhexyl structure (SEHIC).

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23

KITTIVARAPONG, S., C. THEBTARANONTH, and Y. THEBTARANONTH. "ChemInform Abstract: Synthesis of 2-Alkylthio-3-chloro- and 2,3-Bis(alkylthio)propanals." ChemInform 22, no. 14 (2010): no. http://dx.doi.org/10.1002/chin.199114112.

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24

Maślankiewicz, Andrzej, and Stanistaw Boryczka. "4-Alkoxy-3′-(alkylthio)-3,4′-diquinolinyl sulfides and 4-alkoxy-3-(alkylthio) quinolines." Recueil des Travaux Chimiques des Pays-Bas 112, no. 10 (2010): 519–24. http://dx.doi.org/10.1002/recl.19931121002.

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25

Kong, Rui, Zuo Xiao, Fangyuan Xie, Jiaxing Jiang, and Liming Ding. "A D–A copolymer donor containing an alkylthio-substituted thieno[3,2-b]thiophene unit." New Journal of Chemistry 41, no. 8 (2017): 2895–98. http://dx.doi.org/10.1039/c6nj03991j.

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26

Kim, Ji-Hoon, Jong Baek Park, In Hwan Jung, Sung Cheol Yoon, Jeonghun Kwak, and Do-Hoon Hwang. "New alkylthio-thieno[3,2-b]thiophene-substituted benzodithiophene-based highly efficient photovoltaic polymer." Journal of Materials Chemistry C 3, no. 17 (2015): 4250–53. http://dx.doi.org/10.1039/c5tc00627a.

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27

Konečný, Václav, and Štefan Kováč. "A New Electrophilic Rearrangement." Collection of Czechoslovak Chemical Communications 61, no. 3 (1996): 437–41. http://dx.doi.org/10.1135/cccc19960437.

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28

Arakawa, Yuki, Yuko Ishida, Takuma Shiba, Kazunobu Igawa, Shunsuke Sasaki, and Hideto Tsuji. "Effects of alkylthio groups on phase transitions of organic molecules and liquid crystals: a comparative study with alkyl and alkoxy groups." CrystEngComm 24, no. 10 (2022): 1877–90. http://dx.doi.org/10.1039/d1ce01470f.

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29

Plate, Ralf, and Harry C. J. Ottenheijm. "Synthesis of 2-(alkylthio)indoles." Tetrahedron 42, no. 16 (1986): 4511–16. http://dx.doi.org/10.1016/s0040-4020(01)87293-8.

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30

Dabak, Salih, Ahmet Gül, and özer Bekaro??lu. "Hexakis(alkylthio)-Substituted Unsymmetrical Phthalocyanines." Chemische Berichte 127, no. 10 (1994): 2009–12. http://dx.doi.org/10.1002/cber.19941271025.

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31

Yoneda, Shigeo, Kenji Ozaki, Toshihide Inoue, Akira Sugimoto, Kazunori Yanagi, and Masao Minobe. "Novel dimerization reaction of bis(alkylthio)cyclopropenethiones affording tetrakis(alkylthio)thieno[3,4-c]thiophenes." Journal of the American Chemical Society 107, no. 20 (1985): 5801–2. http://dx.doi.org/10.1021/ja00306a037.

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32

Chen, Ted K., and William T. Flowers. "A Facile synthesis of 3-alkylthio-(or arylthio-)pyridines and 3,5-bis(alkylthio)pyridines." Journal of Heterocyclic Chemistry 27, no. 4 (1990): 831–33. http://dx.doi.org/10.1002/jhet.5570270402.

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33

Yang, Ke, Shengfei Dai, Zhi Li, Zhengyi Li та Xiaoqiang Sun. "Amide-assisted α-C(sp3)–H acyloxyation of organic sulfides to access α-acyloxy sulfides". Organic Chemistry Frontiers 8, № 18 (2021): 4974–79. http://dx.doi.org/10.1039/d1qo00774b.

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The direct acyloxyation of 2-(alkylthio)benzamide has been established via an amide-assisted α-C(sp3)–H functionalization in the presence of Selectfluor by using simple carboxylic acid and its corresponding salt as acyloxy sources.

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34

Pietrangeli, Daniela, Sandra Ristori, Angela Rosa, and Giampaolo Ricciardi. "Carboranylporphyrazines for anti-cancer therapies: synthesis and physicochemical properties." Journal of Porphyrins and Phthalocyanines 14, no. 08 (2010): 678–88. http://dx.doi.org/10.1142/s1088424610002574.

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The synthesis, the salient physicochemical properties, and liposome insertion of carboranyl-alkylthio-porphyrazines, a new family of potential BNCT agents, are here reviewed together with recent progresses in their metalation and conversion in the water-soluble counterparts.

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35

Pietrangeli, Daniela, Alexandra V. Soldatova, Daniele Casarini, Angela Rosa, and Giampaolo Ricciardi. "On the flexibility of carboranylalkylthio substituents in porphyrazines and its relevance to the photophysical properties." Inorg. Chem. Front. 1, no. 6 (2014): 464–67. http://dx.doi.org/10.1039/c4qi00055b.

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Ultrafast experiments reveal fast radiationless deactivation of the S<sub>1</sub>(π,π*) state in carboranylalkylthio-porphyrazines, ascribed by DFT/TDDFT and VT <sup>1</sup>H NMR studies to the flexibility of the alkylthio groups.

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36

Filatre-Furcate, Agathe, Pascale Auban-Senzier, Marc Fourmigué, Thierry Roisnel, Vincent Dorcet, and Dominique Lorcy. "Gold dithiolene complexes: easy access to 2-alkylthio-thiazoledithiolate complexes." Dalton Transactions 44, no. 35 (2015): 15683–89. http://dx.doi.org/10.1039/c5dt02534f.

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Reaction of RI with N-tert-butyl-1,3-thiazoline-2-thione derivatives allows the formation of 2-alkylthio-thiazoledithiolate pro-ligands, precursors of Au<sup>III</sup> dithiolene complexes, [Au(RS-tzdt)<sub>2</sub>]<sup>−1,0</sup>.

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37

Tang, Jing, and Xian Huang. "Convenient synthesis of 5-(Arylamino(Alkylthio)Methylene)-2,2-Dimethyl-1,3-Dioxane-4,6-Diones and 2-Arylthio-4-Quinolones." Journal of Chemical Research 2003, no. 3 (2003): 140–41. http://dx.doi.org/10.3184/030823403103173264.

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Meldrum's acid reacted with an aryl isothiocynate and alkyl halides to afford the 5-(arylamino(alkylthio)methylene)-5-methylthio-2,2-dimethyl-1,3-dioxane-4,6-diones and the compounds underwent thermal cyclization to give the 4-2-arylthio-4(1 H)-quinolones

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38

Zou, Yan, Yue Wu, Hang Yang, Yingying Dong, Chaohua Cui, and Yongfang Li. "The effect of alkylthio side chains in oligothiophene-based donor materials for organic solar cells." Molecular Systems Design & Engineering 3, no. 1 (2018): 131–41. http://dx.doi.org/10.1039/c7me00075h.

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The engineering of alkylthio side chains in the molecular conjugated backbone of small molecules is in favor of achieving a linear molecular backbone conformation, slightly red-shifting the absorption spectrum, and down-shifting the HOMO energy level of the resulting molecule.

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39

Gong, Xue, Guangwu Li, Shiyu Feng, et al. "Influence of polymer side chains on the photovoltaic performance of non-fullerene organic solar cells." Journal of Materials Chemistry C 5, no. 4 (2017): 937–42. http://dx.doi.org/10.1039/c6tc04983d.

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The side chains of polymers had a great influence on their molecular packing, energy level, blend morphology and photovoltaic performance. The PCEs of 7.28% and 1.55% were obtained for alkoxy and alkylthio-substituted polymer based non-fullerene solar cells, respectively.

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40

SYED, GHOUSE PEERAN, PRABHAKAR BABU M., and HANUMANTHA REDDY G. "Synthesis of some New (E)-1,2-Bis(alkylthio and alkylsulphonyl) stilbenes." Journal of Indian Chemical Society Vol. 66, Jun 1989 (1989): 412–13. https://doi.org/10.5281/zenodo.6141005.

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Department of Chemistry, Sri Krishnadevaraya University, Anantapur-515 003 <em>Manuscript received 31 October 1988, revised 22 February 1989, accepted 31 March 1989</em> Synthesis of some New (<em>E</em>)-1,2-Bis(alkylthio and alkylsulphonyl) stilbenes 

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41

Schaefer, Ted, Glenn H. Penner, Kerry J. Davie, and Rudy Sebastian. "Control of the orientation of the aldehyde group in 2-(alkylthio)benzaldehydes by the directional lone-pair on sulfur." Canadian Journal of Chemistry 63, no. 3 (1985): 777–81. http://dx.doi.org/10.1139/v85-128.

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The 1H nmr spectral parameters for 2-alkylthio derivatives benzaldehyde (alkyl = CH3, CH2CH3, CH(CH3)2, C(CH3)3) are used to show that the O-syn conformation of the aldehyde group decreases from 40% for the methyl to zero for the tert-butyl compound in CC14 solution at about 300 K. It appears that the alkylthio groups twist out of the benzene plane to the same extent as in the alkyl phenyl sulfides and that it is the concomitant approaches of the 3p lone-pairs on sulfur into the ring plane which, by repulsive interactions with the C=O bond, determine the conformations of the aldehyde group. Th

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42

Zhang, Teng, Hao He, Jun Du, Zhi He, and Shun Yao. "Novel 3-Methyl-2-alkylthio Benzothiazolyl-Based Ionic Liquids: Synthesis, Characterization, and Antibiotic Activity." Molecules 23, no. 8 (2018): 2011. http://dx.doi.org/10.3390/molecules23082011.

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Three series of novel 3-methyl-2-alkylthio benzothiazolyl ionic liquids (ILs) were synthesized for the first time. After structural identification, their melting point, solubility, and thermostability together with antibiotic activity were determined successively. As a result, 3-methyl-2-alkylthio benzothiazolyl p-toluene sulfonate was found to have the highest antibacterial activity among the three series of ILs. Meanwhile, it has a good solubility in water as well. On the basis of comprehensive comparison with similar compounds, the effect of cations and anions of these benzothiazolium ILs o

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43

Sidóová, Eva, Dusan Loos, Helena Bujdáková, and Jana Kallová. "New Anticandidous 2-Alkylthio-6-aminobenzothiazoles." Molecules 2, no. 12 (1997): 36–42. http://dx.doi.org/10.3390/feb97p2.

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44

Er, Hui-Teng, David L. Pole, and John Warkentin. "(Alkylthio)- and (phenylthio)methoxycarbenes from oxadiazolines." Canadian Journal of Chemistry 74, no. 8 (1996): 1480–89. http://dx.doi.org/10.1139/v96-165.

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Four 2-methoxy-5,5-dimethyl-Δ3-1,3,4-oxadiazolines bearing an alkylthio or arylthio group at C2 were prepared. The oxadiazolines undergo thermolysis at 60–80 °C in solution to afford the corresponding oxythiocarbene intermediates. In the absence of carbene traps, dimers of the carbenes were formed. The carbenes were trapped with ethyl crotonate, with dichloromaleic anhydride, with dimethyl acetylenedicarboxylate, and with phenyl isocyanate. Phenyl isocyanate traps methoxy(methylthio)carbene to form two types of adducts, both fundamentally different from the product obtained from reaction of di

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45

Shi, Zurong, Toshiaki Enoki, Kenichi Imaeda, et al. "Thermal properties of tetrakis(alkylthio)tetrathiafulvalenes." Journal of Physical Chemistry 92, no. 17 (1988): 5044–48. http://dx.doi.org/10.1021/j100328a042.

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46

D'yachkova, S. G., N. K. Gusarova, E. A. Beskyrylaya, L. I. Larina, and B. A. Trofimov. "Reaction of (alkylthio)chloroacetylenes with thiourea." Russian Chemical Bulletin 49, no. 7 (2000): 1319. http://dx.doi.org/10.1007/bf02495785.

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47

Zink-Lorre, Nathalie, Enrique Font-Sanchis, Ángela Sastre-Santos, and Fernando Fernández-Lázaro. "Direct alkylthio-functionalization of unsubstituted perylenediimides." Organic & Biomolecular Chemistry 14, no. 39 (2016): 9375–83. http://dx.doi.org/10.1039/c6ob01536k.

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Shi, Zurong, Kenichi Imaeda, Chikako Nakano, Hiroo Inokuchi, Toshiaki Enoki, and Gunzi Saito. "Thermal Expansion of Tetrakis(alkylthio) tetrathiafulvalenes." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 268, no. 1 (1995): 161–72. http://dx.doi.org/10.1080/10587259508031004.

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Imaeda, Kenichi, Tadaoki Mitani, Chikako Nakano, Hiroo Inokuchi, and Gunzi Saito. "Infrared spectra of tetrakis (alkylthio) tetrathiafulvalenes." Chemical Physics Letters 173, no. 4 (1990): 298–302. http://dx.doi.org/10.1016/0009-2614(90)85273-f.

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Phan, Nguyen Huu Trong, and Jeong-Hun Sohn. "Copper-catalyzed aerobic oxidative dehydrogenation for conversion of 2-(alkylthio)-1,4-dihydropyrimidines to 2-(alkylthio)pyrimidines." Tetrahedron 70, no. 43 (2014): 7929–35. http://dx.doi.org/10.1016/j.tet.2014.08.057.

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