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Relevant bibliographies by topics / Phenylthio

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Academic literature on the topic 'Phenylthio'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Phenylthio"

1

King, James Frederick, and Kishan Chand Khemani. "Synthesis and thermolysis of 2-(phenylthio)ethanesulfonyl chloride. The absence of a reported "rearrangement of radicals with migration of the chlorine atom from sulfur to carbon"." Canadian Journal of Chemistry 63, no. 3 (1985): 619–22. http://dx.doi.org/10.1139/v85-101.

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2-(Phenylthio)ethanesulfonyl chloride (1) is the major product of the reaction of (a) lithium 2-(phenylthio)ethanesulfinate (6) and chlorine, and, notwithstanding contrary reports, also of (b) benzenethiol (3) and ethenesulfonyl chloride (4), and (c) sodium 2-(phenylthio)ethanesulfonate (5) and phosphorus pentachloride. The rearrangement referred to in the title, which was proposed to account for the isolation of 2-(phenylthio)ethyl chloride (2) rather than 1 from 3 and 4, therefore does not occur. Desulfonylation of 1 to form 2, however, readily takes place thermally and, in accord with a rat

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2

Jílek, Jiří, Jiří Urban, Petr Taufmann, et al. "Potential antidepressants: 2-(Phenylthio)aralkylamines." Collection of Czechoslovak Chemical Communications 54, no. 7 (1989): 1995–2008. http://dx.doi.org/10.1135/cccc19891995.

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Reactions of 2-(phenylthio)benzyl chloride with dimethylamine, diethylamine, pyrrolidine, piperidine, morpholine, and 1-methylpiperazine afforded the title compounds VI-XI. Reaction of 2-(phenylthio)benzaldehyde with nitromethane gave the nitrostyrene XIV which was reduced with lithium aluminium hydride to 2-(2-(phenylthio)phenyl)ethylamine (XVI). This was transformed to the N-methyl and N,N-dimethyl derivatives XVIII and XIX. The Claisen reaction of (2-(phenylthio)phenyl)acetonitrile with ethyl acetate afforded compound XXI which was cleaved by phosphoric acid to (2-(phenylthio)phenyl)acetone

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3

Deng, Gui-Sheng, Zhi-Zhen Huang, Xiao-Chun Yu та Xian Huang. "Synthesis of α-Phenylthioacylmethylene Triphenylarsoranes and their Wittig-type Reactions". Journal of Chemical Research 23, № 2 (1999): 144–45. http://dx.doi.org/10.1177/174751989902300239.

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α-Phenylthio acylmethylene triphenylarsoranes, the first stable α-thiyl arsonium ylides, are prepared by phenylsulfenylation–transylidation reaction of the corresponding acylmethylene triphenylarsoranes with phenylsulfenyl chloride; Wittig reactions are carried out under mild reaction conditions on the arsonium ylides to provide α-phenylthio-α,β-unsaturated ketones.

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Šindelář, Karel, Zdeněk Šedivý, Marta Hrubantová, Martin Valchář, Jiřina Metyšová, and Miroslav Protiva. "Synthesis of (2-(phenylthio)phenyl)acetamidines and related amidoximes as potential antidepressants." Collection of Czechoslovak Chemical Communications 53, no. 2 (1988): 381–88. http://dx.doi.org/10.1135/cccc19880381.

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Reactions of ethyl(2-(phenylthio)phenyl)acetimidate (X) hydrochloride with ammonia and the corresponding amines resulted in amidines V-X. Heating (2-(phenylthio)phenyl)acetonitrile with 2-aminoethylammonium toluene-4-sulfonate led to the 2-imidazoline XI. Reactions of (2-(phenylthio)phenyl)acetonitrile and the lower homologue with hydroxylamine gave the amidoximes XIII and XV; XIII was oxidized to the sulfoxide XIV. Compounds VII, XI, and XIII showed some antireserpine activity which indicates thymoleptic and antidepressant potentiality. On the other hand, none of the compounds tested did show

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5

Sekine, Mitsuo, and Tsujiaki Hata. "Chemical Synthesis of Oligonucleotides by Use of Phenylthio Group." Current Organic Chemistry 3, no. 1 (1999): 25–66. http://dx.doi.org/10.2174/1385272803666220130205329.

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This review deals with recent studies of oligonucleotide synthesis using the phenylthio group as the phosphate protecting group. Several fundament! properties of the P-S bond in phosphorothioate compounds are described in detail. The chemical synthesis and properties of nucleoside phosphorothioate derivatives, which can be prepared via silyl phosphite intermediates, are described. Several interesting and unique properties of a new useful phosphorylating reagent, S, S-diphenyl phosphorodithioate (PSS) are described with some examples involving an application to oligodeoxyribonucleotide synthesi

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6

OTERA, Junzo. "Methoxy (phenylthio) methane." Journal of Synthetic Organic Chemistry, Japan 44, no. 5 (1986): 459–62. http://dx.doi.org/10.5059/yukigoseikyokaishi.44.459.

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Šindelář, Karel, Vojtěch Kmoníček, Marta Hrubantová, and Zdeněk Polívka. "Substituted N,N-Dimethyl-3-(phenylthio)- and -4-(phenylthio)benzylamines." Collection of Czechoslovak Chemical Communications 57, no. 1 (1992): 194–203. http://dx.doi.org/10.1135/cccc19920194.

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(Arylthio)benzoic acids IIa - IIe and VIb - VId were transformed via the acid chlorides to the N,N-dimethylamides which were reduced either with diborane "in situ" or with lithium aluminium hydride to N,N-dimethyl-(arylthio)benzylamines Ia - Ie and Vb - Vd. Leuckart reaction of the aldehydes IX and X with dimethylformamide and formic acid afforded directly the amines Va and Ve. Demethylation of the methoxy compounds Ia and Ve with hydrobromic acid resulted in the phenolic amines If and Vf. The most interesting N,N-dimethyl-4-(phenylthio)benzylamine (Va) hydrochloride showed affinity to choline

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8

Villa, Mar�a-Jes�s, and Stuart Warren. "[1,4] Phenylthio migrations in the rearrangement of 2,4,4-tris(phenylthio)butanols." Journal of the Chemical Society, Perkin Transactions 1, no. 20 (1994): 2953. http://dx.doi.org/10.1039/p19940002953.

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Schmidt, Bettina, Shrikrishnan Sankaran, Linda Stegemann, Cristian A. Strassert, Pascal Jonkheijm, and Jens Voskuhl. "Agglutination of bacteria using polyvalent nanoparticles of aggregation-induced emissive thiophthalonitrile dyes." Journal of Materials Chemistry B 4, no. 27 (2016): 4732–38. http://dx.doi.org/10.1039/c6tb01210h.

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V., BALIAH, and APARAJITHAN K. "Dipole Moments and UV Spectra of some Long-chain Molecules." Journal Of Indian Chemical Society Vol. 69, May 1992 (1992): 255–59. https://doi.org/10.5281/zenodo.6087488.

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Department of Chemistry, Annamalai University, Annamalainagar-608 002  <em>Manuscript received 8 October 1991, accepted 1 April 1992</em> About one hundred compounds with long-chain molecular structure have been prepared (most of them are new). The dipole moments of fou \(\alpha,\omega-bis\)(p-methoxyphenylthio)alkanes and five \(\alpha,\omega-bis\)(<em>p</em>-methoxyphenylsulphonyl)aikanes have been determined to find the<em> </em>effect of chain-length. In the case of the sulphones, the observed values are compared with the values calculated for free rotation around all bonds inter

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Dissertations / Theses on the topic "Phenylthio"

1

Hannaby, M. P. "Phenylthio-controlled migrations around rings." Thesis, University of Cambridge, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355872.

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Aggarwal, V. K. "Stereocontrolled synthesis with phenylthio migration." Thesis, University of Cambridge, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383037.

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Coldham, Iain. "Stereocontrolled cyclic amine synthesis by phenylthio migration." Thesis, University of Cambridge, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315736.

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Sansbury, Francis Hugh. "Stereospecific cyclic ether formation with phenylthio migration." Thesis, University of Cambridge, 1991. https://www.repository.cam.ac.uk/handle/1810/273136.

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5

Parham, Karol Renee. "Carbon Alkylation of 2-Phenylthio-1,3-cyclopentanediones." W&M ScholarWorks, 1986. https://scholarworks.wm.edu/etd/1539625347.

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Chibale, Kelly. "Asymmetric aldol reactions and phenylthio migrations in synthesis." Thesis, University of Cambridge, 1992. https://www.repository.cam.ac.uk/handle/1810/272239.

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Amoozadeh, Ali. "Photochemical rearrangement of 2-phenylthio-3-aminocyclohexanols, new access to deoxyazasugars and their derivatives." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0025/NQ52123.pdf.

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8

Rautschek, Julia [Verfasser], Peter [Gutachter] Metz, and Hans-Joachim [Gutachter] Knölker. "Ein enantioselektiver Zugang zu Morphinan-Alkaloiden durch temporäre Phenylthio-Derivatisierung / Julia Rautschek ; Gutachter: Peter Metz, Hans-Joachim Knölker." Dresden : Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2018. http://d-nb.info/1226813135/34.

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Forteath, Shaun. "Photophysicochemical studies of phenylthio phthalocyanines interaction with gold nanoparticles and applications in dye sensitised solar cells and optical limiting." Thesis, Rhodes University, 2012. http://hdl.handle.net/10962/d1004995.

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The syntheses, spectroscopic characterisation, photophysical and photochemical studies have been conducted for a variety of phenylthio substituted phthalocyanines (Pcs). Comparisons have been made taking into consideration the influence of the central metal ion, solvent properties and substituent type. The optical limiting properties were also determined for all the Pcs synthesised. A low-symmetry metallophthalocyanine complex was similarly characterised and the photoelectrochemical parameters determined when used as a sensitiser of nanoporous ZnO. The symmetric analogue was conjugated to gold

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10

Nguyen, Van Dong. "Speciation analysis of butyl- and phenyltin compounds in environmental samples by GC separation and atomic spectrometric detection." Doctoral thesis, Umeå : Department of Chemistry, Umeå University, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-892.

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Book chapters on the topic "Phenylthio"

1

Kimura, Makoto, Hirotaka Kawai, and Yasuhiko Sawaki. "Ring Opening Reaction of Phenylthio-Cyclopropanes by Anodic or Photochemical One-Electron Oxidation." In Novel Trends in Electroorganic Synthesis. Springer Japan, 1998. http://dx.doi.org/10.1007/978-4-431-65924-2_22.

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2

Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with 1,2-bis-[o-(2-hydroxy-5-methylphenylazo)phenylthio]ethane." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_102.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with 1,2-bis-[o-(2-hydroxy-5-methylphenylazo)phenylthio]propane." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_104.

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4

Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with 1,2-bis-[o-(2-hydroxy-5-chlorophenylazo)phenylthio]ethane." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_106.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with 1,2-bis-[o-(2-hydroxy-5-chlorophenylazo)phenylthio]propane." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_108.

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6

Jyothi, N. Rama, P. Snehalatha, and S. Lakshmi Narayana. "9H-Carbazole-3-carbaldehyde-4-phenylthiosemicarbazone, 10-Hexyl-10-H-phenothiazine-3-carbaldehyde-4-phenylthio semicarbazone and 2-Thiophenecarboxaldehyde-4-Methylthiosemicarbazone and their Metal Complexes: Synthesis and Anti-bacterial Activity Studies." In Novel Aspects on Chemistry and Biochemistry Vol. 3. B P International (a part of SCIENCEDOMAIN International), 2023. http://dx.doi.org/10.9734/bpi/nacb/v3/4372c.

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7

Marques Raposo, Maria Manuela, Susana Paula Graça da Costa, and Rosa Maria Ferreira Batista. "12.2.1. Synthesis of 2-(5-Phenylthien-2′-yl)benzothiazole." In Comprehensive Organic Chemistry Experiments for the Laboratory Classroom. The Royal Society of Chemistry, 2016. http://dx.doi.org/10.1039/9781849739634-00730.

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Conference papers on the topic "Phenylthio"

1

Meerovich, Igor G., Valentina M. Derkacheva, Gennady A. Meerovich, et al. "Phenylthio-substituted phthalocyanines as new photosensitizers for photodynamic therapy." In Biomedical Optics (BiOS) 2007, edited by David Kessel. SPIE, 2007. http://dx.doi.org/10.1117/12.697426.

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2

Pan, Sujuan, Pingping Shen, Dongdong Ma, et al. "The effect of metal ions on the photophysical and photochemical property of phenylthio bromo metal phthalocyanines." In SPIE/COS Photonics Asia, edited by Qingming Luo, Xingde Li, Ying Gu, and Yuguo Tang. SPIE, 2016. http://dx.doi.org/10.1117/12.2246161.

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3

Inthajak, Krit, Nirattaya Khamsemanan, Cholwich Nattee, Pisanu Toochinda, and Luckhana Lawtrakul. "Quantiative structure-activity relationship analysis of 1-[(2-Hydroxyethoxy)methyl]-6-(phenylthio)thymine (HEPT) analogues with the use of random forest." In 2016 Second Asian Conference on Defence Technology (ACDT). IEEE, 2016. http://dx.doi.org/10.1109/acdt.2016.7437664.

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4

Sun, Yuan-Wan, Thomas L. Olson, Chul-Hoon Kwon, and Kun-Ming Chen. "Abstract 4576: Quantitative proteomic analysis of 2-({4-[4-(acridin-9-ylamino)phenylthio]phenyl}(2-hydroxyethyl)amino)ethan-1-ol (CK0402) modulated protein expression in breast cancer SKBR-3 cells." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-4576.

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