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Journal articles on the topic 'Ethylthio'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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1

Shaw, David R., Thomas F. Peeper, and Robert L. Westerman. "Persistence of Phytotoxicity of Metribuzin and Its Ethylthio Analog." Weed Science 34, no. 3 (1986): 409–12. http://dx.doi.org/10.1017/s0043174500067084.

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The persistence of biologically active metribuzin [4-amino-6-(1,1-dimethylethyl)-3-(methylthio)-1,2,4-triazin-5(4H)-one] and its ethylthio analog [4-amino-6-(1,1-dimethylethyl)-3-(ethylthio)-1,2,4-triazin-5(4H)-one] were compared using an intact-plant chlorophyll fluorescence bioassay technique with oats (Avena sativaL.) and wheat (Triticum aestivumL.). Degradation of metribuzin phytotoxicity at concentrations of 0 to 1 ppm (w/w) ai in a Pond Creek silt loam soil was linear over time, with a half-life of 8 days at 35 C. Initial degradation of the biologically active ethylthio analog was much m

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2

Ratliff, Randall L., and Thomas F. Peeper. "BromusControl in Winter Wheat (Triticum aestivum) with the Ethylthio Analog of Metribuzin." Weed Technology 1, no. 3 (1987): 235–41. http://dx.doi.org/10.1017/s0890037x00029602.

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Twenty field experiments were conducted in Oklahoma from 1983 through 1986 to evaluate the ethylthio analog of metribuzin [4-amino-6-(1,1-dimethylethyl)-3-(ethylthio)-1,2,4-triazin-5(4H)-one] for selective control of cheat (Bromus secalinusL. #3BROSE), downy brome (Bromus tectorumL. # BROTE), and rescuegrass (Bromus catharticusVahl. # BROCA) in winter wheat (Triticum aestivumL.). The ethylthio analog of metribuzin applied postemergence at 1.1 kg ai/ha before the weeds tillered controlled 91 to 100% of theseBromusspp. in winter wheat. Control of tilleredBromusspp. was less consistent. AsBromuss

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3

Pietrangeli, Daniela, Gaetano Garramone, Maria Rachele Guascito, Antonietta Pepe, Angela Rosa, and Giampaolo Ricciardi. "Synthesis, coordination chemistry, and physico-chemical properties of the 2-chloroethoxy-iron(III)(ethylthio) porphyrazine." Journal of Porphyrins and Phthalocyanines 17, no. 08n09 (2013): 870–80. http://dx.doi.org/10.1142/s1088424613500685.

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Reaction of octakis(ethylthio)porphyrazine ( H 2 OESPz ) with FeBr 2 in ClCH 2 CH 2 OH at 135 °C affords the 2-chloroethoxy-iron(III)-(ethylthio)porphyrazine, ( ClCH 2 CH 2 O ) Fe III OESPz , ( LFe III OESPz ) in good yield. The spectroscopic, redox, and coordination properties of the complex and its μ-oxo dimer derivative, [ Fe III OESPz ]2 O , are investigated and compared to those of the iron(III)porphyrin analogs.

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4

Riera, X., V. Moreno, M. Font-Bardia, and X. Solans. "Pd(II) and Pt(II) complexes with 2-(ethylthio)ethylamine. Crystal structure of [Pd(2-(ethylthio)ethylamine)Cl2] and [Pd(2-(ethylthio)ethylamine)2](ClO4)2." Polyhedron 18, no. 1-2 (1998): 65–73. http://dx.doi.org/10.1016/s0277-5387(98)00268-x.

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5

Yahiro, Shuhei, Keisuke Shibata, Takeshi Saito, Tatsuo Okauchi та Toru Minami. "Acid-Promoted Reaction of Trimethylsilylketene Bis(ethylthio)acetal with Imines. Synthesis of γ,γ-Bis(ethylthio)allylamines". Journal of Organic Chemistry 68, № 12 (2003): 4947–50. http://dx.doi.org/10.1021/jo020748v.

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6

Okauchi, Tatsuo, Tatsuyoshi Tanaka та Toru Minami. "Lewis Acid-Promoted Deoxygenative Di[β,β-bis(ethylthio)]vinylation of Aldehydes with Trimethylsilylketene Bis(ethylthio)acetal". Journal of Organic Chemistry 66, № 11 (2001): 3924–29. http://dx.doi.org/10.1021/jo010007e.

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7

Kimura, S., H. Nii, H. Kurai, and T. Mori. "Oxygen containing tetrathiapentalene derivative having ethylthio chains." Synthetic Metals 133-134 (March 2003): 365–66. http://dx.doi.org/10.1016/s0379-6779(02)00303-x.

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8

Yu, Haifeng, Yongmei Zhang, Tiechun Li та ін. "Vilsmeier cyclization of α-acetyl-α-aroyl ketene-N,S-acetals: direct and efficient synthesis of halogenated pyridin-2(1H)-ones". RSC Advances 5, № 15 (2015): 11293–96. http://dx.doi.org/10.1039/c4ra14626c.

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9

Okauchi, Tatsuo, Tatsuyoshi Tanaka та Toru Minami. "ChemInform Abstract: Lewis Acid Promoted Deoxygenative Di[β,β-bis(ethylthio)]vinylation of Aldehydes with Trimethylsilylketene Bis(ethylthio)acetal." ChemInform 32, № 42 (2010): no. http://dx.doi.org/10.1002/chin.200142093.

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10

Tao, Ye, You Li, Xu-Hong Pang, et al. "Four CuI(ett) coordination polymorphs and changes in XRD upon hydrothermal condition optimization." CrystEngComm 19, no. 41 (2017): 6146–53. http://dx.doi.org/10.1039/c7ce01595j.

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11

Bates, Gordon S., and S. Ramaswamy. "A formal [1,3] sigmatropic reaction involving free radical intermediates: a mechanistic investigation." Canadian Journal of Chemistry 63, no. 3 (1985): 745–54. http://dx.doi.org/10.1139/v85-123.

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The quantitative isomerization of 2,2-bis(ethylthio)-3,3-dimethylpent-4-enal to 2,2-bis(ethylthio)-5-methylhex-4-enal was studied over the temperature range 130–170 °C. An investigation of the generality and specific mechanism of this formal [1,3] sigmatropic shift was conducted with six related compounds. The rearrangements were found to obey first-order kinetics, and on the basis of significant positive entropies of activation (52–106 J deg−1 mo−1), crossover and trapping experiments, and the lack of a solvent effect (decane vs. DMF), an intermolecular, free-radical chain pathway has been pr

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12

Yu, Haifeng, Tiechun Li, Peiqiu Liao, Quanping Diao, Guang Xin, and Dongyan Hou. "Acidity-Controlled Indolylation of 3, 3-Bis(ethylthio)acrylate." Chinese Journal of Organic Chemistry 34, no. 5 (2014): 956. http://dx.doi.org/10.6023/cjoc201312020.

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13

Kimura, Shinya, Hirofumi Nii, Hiroyuki Kurai, Tomoaki Takeuchi, Mao Katsuhara, and Takehiko Mori. "Ethylenedioxy-Containing Tetrathiapentalene Derivative with Ethylthio Chains, C2TEO-TTP." Bulletin of the Chemical Society of Japan 76, no. 1 (2003): 89–96. http://dx.doi.org/10.1246/bcsj.76.89.

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14

Baggio, R., D. Vega, M. L. Aimar, R. H. de Rossi, and J. Ellena. "4-Benzyl-5-ethylthio-3H-1,2-dithiole-3-thione." Acta Crystallographica Section C Crystal Structure Communications 53, no. 8 (1997): 1125–27. http://dx.doi.org/10.1107/s0108270197003697.

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15

El-Bahaie, Said, Mohamed G. Assy, and Azza Kadry. "Synthesis and reactions of 2-(2-arylvinyl) pyrimidines." Collection of Czechoslovak Chemical Communications 55, no. 4 (1990): 1049–54. http://dx.doi.org/10.1135/cccc19901049.

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2-(2-Arylvinyl)-4-mercapto-5-acetylpyrimidines IIIa-IIId were synthesized by condensation of cinnamoyl isothiocyanates Ia-Id with 2-aminopent-2-ene-4-one II. The synthesis of 4-methylthio-, 4-(β-cyano)ethylthio- and 4-oxopyrimidines is also described. Compounds IV reacted with hydrazine hydrate to yield the corresponding pyrazolopyrimidine.

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16

Ishikawa, T. I., A. Takenaka, Y. Sasada, and M. Ohki. "Structure of 2-[2-(thymin-1-yl)ethylthio]acetic acid." Acta Crystallographica Section C Crystal Structure Communications 42, no. 7 (1986): 860–61. http://dx.doi.org/10.1107/s0108270186094283.

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17

Tsuchiya, Y., A. Takenaka, Y. Sasada, and M. Ohki. "Structure of 1-{2-[2-(4-hydroxyphenyl)ethylthio]ethyl}thymine." Acta Crystallographica Section C Crystal Structure Communications 42, no. 7 (1986): 821–23. http://dx.doi.org/10.1107/s0108270186094416.

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18

Mammadbeyli, E. G., I. A. Jafarov, S. I. Ibrahimli, T. G. Kyazimova, S. T. Alieva, and G. F. Mamedova. "Synthesis and antimicrobial activity of aminomethoxy-substituted 1-(ethylthio)heptanes." Russian Journal of General Chemistry 83, no. 3 (2013): 481–84. http://dx.doi.org/10.1134/s1070363213030134.

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19

Gonzalez, M. E., M. J. Almela, M. Yacout, and L. Carrasco. "6-(3,4-Dichlorophenoxy)-3-(ethylthio)-2-pyridincarbonitrile inhibits poliovirus uncoating." Antimicrobial Agents and Chemotherapy 34, no. 6 (1990): 1259–61. http://dx.doi.org/10.1128/aac.34.6.1259.

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20

Wu, You-Chi Mason, and Timothy M. Swager. "Living Polymerization of 2-Ethylthio-2-oxazoline and Postpolymerization Diversification." Journal of the American Chemical Society 141, no. 32 (2019): 12498–501. http://dx.doi.org/10.1021/jacs.9b06009.

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21

Wilcut, John W. "Efficacy and Economics of Common Bermudagrass (Cynodon dactylon) Control in Peanut (Arachis hypogaea)." Peanut Science 18, no. 2 (1991): 106–9. http://dx.doi.org/10.3146/i0095-3679-18-2-11.

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Abstract Field experiments were conducted in 1988 and 1989 to evaluate various postemergence graminicides for common bermudagrass (Cynodon dactylon (L). Pers.) control in peanuts (Arachis hypogaea). A single application of fluazifop-P [(R)-2-[4[[5-(trifluorornethyl)-2-pyridinyl]oxy]phenoxy]propanoic acid] or clethodim [(E, E)-(±)-2-[1-[[(3-chloro-2-propenyl)oxy]imino] propyl]-5-[2-ethylthio)propyl]-3-hydroxy-2-cyclohexen-1-one] controlled approximately 25 to 30% more common bermudagrass than a single application of sethoxydim (2-[1-(ethoxyimino) butyl]-5-[2-(ethylthio)propyl]-3-hydroxy-2-cyclo

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22

Paulitz, Christian, та Wolfgang Steglich. "Stereoselective Modification of a Cyclopentapeptide via an α-(Ethylthio)glycine Residue†". Journal of Organic Chemistry 62, № 24 (1997): 8474–78. http://dx.doi.org/10.1021/jo971295a.

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23

Baggio, R., L. L. Aimar, R. H. de Rossi, and L. Suescun. "5-R-3H-1,2-Dithiole-3-thione (R= Ethylthio and Methylthio)." Acta Crystallographica Section C Crystal Structure Communications 54, no. 12 (1998): 1902–5. http://dx.doi.org/10.1107/s0108270198007793.

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24

Nesměrák, K., M. Pospíšek, B. Zikánová, I. Němec, J. Barbe, and J. Gabriel. "Effect of structure on antibiotic action of new 9-(ethylthio)acridines." Folia Microbiologica 47, no. 2 (2002): 118–20. http://dx.doi.org/10.1007/bf02817668.

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25

Makhmudov, U. S., K. K. Turgunov, B. Tashkhodzhaev, V. A. Saprykina, and Kh M. Shakhidoyatov. "Crystalsolvates of N-(3-ethylthio-1,2,4-thiadiazol-5-yl-aminocarbonylmethyl)cytisine." Chemistry of Natural Compounds 44, no. 4 (2008): 466–71. http://dx.doi.org/10.1007/s10600-008-9098-8.

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26

Oparin, D. A. "1-Ethylthio-2,3,3-triarylisoindolinium salts and their reactions with nucleophilic reagents." Chemistry of Heterocyclic Compounds 23, no. 2 (1987): 165–68. http://dx.doi.org/10.1007/bf00663854.

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27

Bridges, David C., and J. M. Chandler. "Effect of Herbicide and Weed Height on Johnsongrass (Sorghum halepense) Control and Cotton (Gossypium hirsutum) Yield." Weed Technology 1, no. 3 (1987): 207–11. http://dx.doi.org/10.1017/s0890037x00029547.

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Research was conducted from 1983 through 1985 in east central Texas to determine the effect of grass-specific herbicides, herbicide rates, and weed height on johnsongrass [Sorghum halepense(L.) Pers. #3SORHA] control and cotton (Gossypium hirsutumL. 'Stoneville 825’) yield. Seven herbicides were applied to johnsongrass less than 30 cm tall with 2 to 5 leaves approximately 4 weeks after cotton emergence. Good-to-excellent johnsongrass control was observed for each herbicide except cloproxydim {(E,E)-2-[l-[[(3-chloro-2-propenyl)oxy]imino] butyl]-5-[2-(ethylthio)propyl]-3-hydroxy-2-cyclohexen-1-o

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28

Bryson, Charles T. "Effects of Rainfall on Foliar Herbicides Applied to Rhizome Johnsongrass." Weed Science 35, no. 1 (1987): 115–19. http://dx.doi.org/10.1017/s0043174500026886.

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A rainfall simulator was used to evaluate the effects of washoff on 10 foliar-applied herbicides on johnsongrass [Sorghum halepense(L.) Pers. # SORHA] in greenhouse experiments during 1983 and 1984 at Stoneville, MS. Time intervals between herbicide application and rainfall ranged from 20 to 240 min. Johnsongrass topgrowth control was equivalent to rain-free treatments using DPX-Y6202 {ethyl [2-[4-(6-chloro-2-quinozalinyl)oxy] phenoxy] propionate} at 0.03 and 0.06 kg/ha at time periods of 90 and 40 min between herbicide application and rainfall, respectively, at 28 days after treatment (DAT).

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29

Barlin, GB, LP Davies, RA Davis, and PW Harrison. "Imidazo[1,2-b]pyridazines. XVII. Synthesis and Central Nervous System Activity of Some 6-(Alkylthio and chloro)-3-(methoxy, unsubstituted and benzamidomethyl)-2-arylimidazo[1,2-b]pyridazines Containing Methoxy, Methylenedioxy and Methyl Substituents." Australian Journal of Chemistry 47, no. 11 (1994): 2001. http://dx.doi.org/10.1071/ch9942001.

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Syntheses are reported for 6-( methylthio, ethylthio, propylthio, substituted benzylthio and chloro )-3-( methoxy, unsubstituted and benzamidomethyl )-2-arylimidazo[1,2-b] pyridazines containing methoxy, methylenedioxy and methyl groups attached to phenyl substituents . In tests of the ability of these compounds to displace [3H]diazepam from rat brain membranes, 3-methoxy-6-(3′,4′-methylenedioxybenzylthio)-2- (3′,4′-methylenedioxyphenyl) imidazo [1,2-b] pyridazine (IC50 1 nM) bound most strongly; methylenedioxy groups were beneficial to activity whereas polymethoxy or dimethyl substituents wer

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30

Başeren, Şükran Cenikli, Şennur Özçelik, and Ahmet Gül. "Boronic esters of a porphyrazine and its precursor." Journal of Porphyrins and Phthalocyanines 15, no. 07n08 (2011): 742–47. http://dx.doi.org/10.1142/s1088424611003677.

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Phenylboronic acid esters of an unsaturated precursor 1,2-dicyano-1,2-bis(2-hydroxy- ethylthio)ethylene and the magnesium porphyrazine derived from it have been prepared either by refluxing a mixture of the reagents in chloroform in the presence of molecular sieve or by solvent-free heating in an oven under reduced pressure. The two novel compounds have been characterized by elemental analysis together with ultraviolet-visible, infrared spectroscopy, proton nuclear magnetic resonance, carbon-13 nuclear magnetic resonance, boron-11 nuclear magnetic resonance, and mass spectra.

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31

Yu, Haifeng, Wenju Wang, Kehua Wang та Xue Zhang. "Complementary and Regioselective Synthesis of Isomeric 3-[Isoxazol-3(or 5)-yl]indoles from β-Ethylthio-β-indolyl-α,β-unsaturated Ketones". Synthesis 53, № 11 (2021): 1989–99. http://dx.doi.org/10.1055/s-0040-1706658.

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AbstractA simple and efficient method for the complementary and regioselective synthesis of isomeric 3-(isoxazol-5-yl)indoles and 3-(isoxazol-3-yl)indoles has been developed by the regioselective cyclocondensation reaction of β-ethylthio-β-indolyl-α,β-unsaturated ketones and hydroxylamine hydrochloride. It was found that the cyclocondensation reaction in the presence of excess NaOEt in refluxing EtOH gives 3-(isoxazol-5-yl)indoles in good yields, whereas using NaOAc in boiling AcOH gives 3-(isoxazol-3-yl)indoles in good yields.

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32

Rodrigues, Daniel N. S., Lucas C. Ducati, Paulo R. Olivato, and Maurizio Dal Colle. "Conformational Analysis and Electronic Interactions of Some 4′-Substituted-2-ethylthio-phenylacetates." Journal of Physical Chemistry A 119, no. 16 (2015): 3823–32. http://dx.doi.org/10.1021/acs.jpca.5b01531.

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33

Ge, Maofa, Jing Wang, Xinjiang Zhu, Zheng Sun, and Dianxun Wang. "Experimental and theoretical studies on different ionic states of ethylthio CH3CH2S radical." Journal of Chemical Physics 113, no. 5 (2000): 1866–69. http://dx.doi.org/10.1063/1.481990.

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34

Verkruijsse, H. D., and L. Brandsma. "A Simple and Safe Procedure for Bis(methylthio)- and Bis(ethylthio)acetylene." Synthesis 1991, no. 10 (1991): 818. http://dx.doi.org/10.1055/s-1991-26578.

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35

TRISHIN, YU G., A. F. AFANASOV, I. A. LITVINOV, V. A. NAUMOV, and V. N. CHISTOKLETOV. "ChemInform Abstract: Reaction of Diethyl 2-Chloro-2-(ethylthio)ethenylphosphonite with Nitrilimines." ChemInform 23, no. 34 (2010): no. http://dx.doi.org/10.1002/chin.199234232.

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36

Luger, Peter, and Klaus Roth. "X-Ray, n.m.r., and theoretical studies of the structures of (ethylthio)bullvalene." Journal of the Chemical Society, Perkin Transactions 2, no. 6 (1989): 649. http://dx.doi.org/10.1039/p29890000649.

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37

Matsubara, Yoshio, Kazutada Kitano, You Sasaki, Masakuni Yoshihara, and Toshihisa Maeshima. "Crystal and Molecular Structure of 2-Ethylthio-3-phenyl-1,3,4-thiadiazolium Tetrafluoroborate." Bulletin of the Chemical Society of Japan 66, no. 11 (1993): 3525–27. http://dx.doi.org/10.1246/bcsj.66.3525.

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38

Lee, Jung-Si, Kuo-Chih Huang, Wen-Jwu Wang, and Gene-Hsiang Lee. "Crystal structure and physical properties of 1,3,6,8-tetrakis(ethylthio)pyrene-Qmnt complex." Synthetic Metals 70, no. 1-3 (1995): 1231–32. http://dx.doi.org/10.1016/0379-6779(94)02832-j.

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39

Willard, T. R., C. M. Peacock, and D. G. Shilling. "Photosynthesis as an Index of Turfgrass Growth Following Application of Herbicides." HortScience 25, no. 4 (1990): 451–53. http://dx.doi.org/10.21273/hortsci.25.4.451.

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The effects of sethoxydim, cloproxydim, and fluazifop on photosynthesis and growth of St. Augustinegrass [Stenotaphrum secundatum (Walt.) Kuntze `Floralawn'], bahiagrass (Paspalum notatum var. saurae Parodi `Pensacola'), and centipedegrass [Eremochloa ophiuroides (Munro.) Hack.] were evaluated to determine if photosynthesis could be used as a rapid, nondestructive measure of relative susceptibility. Field and greenhouse studies were conducted using infrared CO2 analysis to estimate photosynthesis. Under field conditions, St. Augustinegrass was susceptible to sethoxydim and fluazifop applicatio

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40

Hartke, Klaus, and Frank Rauschen. "Zur Reaktion von Trialkylphosphiten mit dem Titanocen-Komplex des 4,5-Dimercapto-1,3-dithiol-2-ons / Reaction of Trialkyl Phosphites with the Titanocene Complex of 4,5-Dimercapto-1,3-dithiole-2-one." Zeitschrift für Naturforschung B 51, no. 11 (1996): 1611–17. http://dx.doi.org/10.1515/znb-1996-1114.

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The titanocene complex 1b reacts with triethyl and trimethyl phosphite to yield the phosphonoesters 3a,b, which exist in solution as a mixture of two interconvertable conformers. The titanocene complex la is alkylated by trimethyloxonium tetrafluoroborate to form the 1,3-dithiolium tetrafluoroborate 10. The latter interacts with 9 (the lithium salt of 3a) merely by proton transfer restoring 3a. 9 condenses with aldehydes and ketones in a Horner- Wadsworth-Emmons reaction to give the titanocene complexes 16 as main products and the 4.5-bis(ethylthio)-1,3-dithiole-2-ylidene compounds 17 as bypro

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41

Riley, Dennis P., and Joel D. Oliver. "Ruthenium(II)-catalyzed thioether oxidation. 2. Syntheses and crystal structures of two ruthenium(II) complexes with the new linear tridentate ligand 3-(ethylthio)-1-((3-(ethylthio)propyl)sulfinyl)propane." Inorganic Chemistry 25, no. 11 (1986): 1821–25. http://dx.doi.org/10.1021/ic00231a022.

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42

Campbell, James R., and Donald Penner. "Abiotic Transformations of Sethoxydim." Weed Science 33, no. 4 (1985): 435–39. http://dx.doi.org/10.1017/s0043174500082606.

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The fate of14C-sethoxydim {2-[1-(ethoxyimino) butyl]-5-[2-(ethylthio)propyl]-3-hydroxy-2-cyclohexen-1-one} in an aqueous solution and on glass exposed to light was evaluated. Within 1 h, more than 80% of the14C-sethoxydim was transformed to six major products. Qualitatively the transformations were similar for both systems, and a single end product constituted the majority of14C after 72 h. Two transitory compounds were found to be phytotoxic to barnyardgrass [Echinochloa crus-galli(L.) Beauv. ♯ ECHCG] and were more stable than sethoxydim. A nonphytotoxic compound isolated and identified by ma

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43

Özçeşmeci, İbrahim, Orhan Güney, Ali İhsan Okur, and Ahmet Gül. "New phthalocyanines containing bulky electron rich substituents." Journal of Porphyrins and Phthalocyanines 13, no. 06 (2009): 753–59. http://dx.doi.org/10.1142/s1088424609000838.

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Metal-free and metallophthalocyanines with four 9-anthroyl groups bound through ethylthio ester bridges on the periphery have been prepared. The new compounds were characterized by elemental analyses, 1 H NMR, IR, mass and UV-vis spectral data. The electronic spectra exhibit an intense π-π* transition of 9-anthroyl identity together with characteristic Q and B bands of the phthalocyanine core. Effect of metal ions on intensity of fluorescence spectra of phthalocyanine derivatives substituted with 9-anthroyl groups was investigated. The energy transfer to the phthalocyanine core and radiative d

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44

Sastre, Juan A. López, José Molina Molina, Dolores Portal Olea, and Cristina Romero-Avila. "A new synthesis of 2,5-anhydro-D-mannose derivatives." Canadian Journal of Chemistry 66, no. 12 (1988): 2975–80. http://dx.doi.org/10.1139/v88-462.

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Penta-O-acetyl-D-glucose diethyl dithioacetal monoxide 3 was obtained by oxidation of penta-O-acetyl-D-glucose diethyl dithioacetal 2 with 3-chloroperbenzoic acid. By reaction of 3 with sodium methoxide in methanol and further acetylation, 3,4,6-tri-O-acetyl-2,5-anhydro-D-mannose-diethyl dithioacetal monoxide 8 and the reduction product 3,4,6-tri-O-acetyl-2,5-anhydro-1,1-bis(ethylthio)-1-deoxy-D-arabino-hex-1-enitol 4 were obtained. Reduction of 8 yielded the corresponding dithioacetal derivative 9, which was converted to 3,4,6-tri-O-acetyl-2,5-anhydro-D-mannose diethyl acetal 11.

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Ebright, Yon W., Yan Chen, Younggyu Kim, and Richard H. Ebright. "S-[2-(4-Azidosalicylamido)ethylthio]-2-thiopyridine: Radioiodinatable, Cleavable, Photoactivatible Cross-Linking Agent." Bioconjugate Chemistry 7, no. 3 (1996): 380–84. http://dx.doi.org/10.1021/bc9600168.

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Iwatsuki, Shouji, Takahito Itoh, Naoko Kusaka, and Hajime Maeno. "Radical polymerization behavior of 7,8-bis(ethylthio)- and 7,8-bis(phenylthio)-7,8-dicyanoquinodimethanes." Macromolecules 25, no. 24 (1992): 6395–99. http://dx.doi.org/10.1021/ma00050a002.

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Luheshi, Abdul-Basset N., Robert K. Smalley, P. D. Kennewell, and R. Westwood. "1,3-Dipolar cycloadditions of 2-ethoxy- and 2-(ethylthio)-1-azetines with nitrilimines." Tetrahedron Letters 31, no. 1 (1990): 127–30. http://dx.doi.org/10.1016/s0040-4039(00)94352-1.

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Yun, Mikyung, Youngsook Shin, Shinsook Yoon, Keun Ho Chun та Jeong E. Nam Shin. "ChemInform Abstract: Syntheses of Mannosidic Disaccharides from Derivatives of Ethylthio α-D-Mannopyranoside." ChemInform 30, № 16 (2010): no. http://dx.doi.org/10.1002/chin.199916212.

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Dubinina, Tatiana V., Pavel I. Tychinsky, Nataliya E. Borisova, et al. "Lanthanide (III) complexes of 3-(ethylthio)phenyl-substituted phthalocyanines: Synthesis and physicochemical properties." Dyes and Pigments 156 (September 2018): 386–94. http://dx.doi.org/10.1016/j.dyepig.2018.04.028.

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Bonnema, J., and J. F. Arens. "Chemistry of acetylenic ethers XLV: Some reactions of esters of (ethylthio)propynoic acid." Recueil des Travaux Chimiques des Pays-Bas 79, no. 11 (2010): 1137–49. http://dx.doi.org/10.1002/recl.19600791108.

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