Log in

Relevant bibliographies by topics / Phenylthio / Journal articles

To see the other types of publications on this topic, follow the link: Phenylthio.

Journal articles on the topic 'Phenylthio'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Phenylthio.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

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.

Full text

Abstract:

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.

APA, Harvard, Vancouver, ISO, and other styles

4

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

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.

Full text

Abstract:

(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

APA, Harvard, Vancouver, ISO, and other styles

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

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.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

11

Eiden, Fritz, and Ulrike Grusdt. "4-Phenylthio-3-pyrrolcarbonsäureester." Archiv der Pharmazie 320, no. 10 (1987): 1020–31. http://dx.doi.org/10.1002/ardp.198700005.

Full text

APA, Harvard, Vancouver, ISO, and other styles

12

SINDELAR, K., V. KMONICEK, M. HRUBANTOVA, and Z. POLIVKA. "ChemInform Abstract: Substituted N,N-Dimethyl-3-(phenylthio)- and -4-(phenylthio) benzylamines." ChemInform 23, no. 19 (2010): no. http://dx.doi.org/10.1002/chin.199219145.

Full text

APA, Harvard, Vancouver, ISO, and other styles

13

Mak, Thomas C. W., Yip Wai-Hing, Chan Wing-Hong, Colin H. L. Kennard, Graham Smith, and Eric J. O'Reilly. "Metal-(phenylthio)alkanoic acid interactions—X. The crystal structures of thallium(I) (phenylthio)acetate(phenylthio)acetic acid adduct, caesium (2,4-dichloro-5-methylphenylthio)acetate(2,4-dichloro-5-methylphenylthio)acetic acid adduct, caesium (phenylthio)acetate(phenylthio)acetic acid adduct and caesium 2-(phenylthio)propionate monohydrate." Polyhedron 8, no. 6 (1989): 793–800. http://dx.doi.org/10.1016/s0277-5387(00)83848-6.

Full text

APA, Harvard, Vancouver, ISO, and other styles

14

Paoli-Lombardo, Romain, Nicolas Primas, Sébastien Hutter, et al. "6-Chloro-3-nitro-8-(phenylthio)-2-[(phenylthio)methyl] imidazo[1,2-a]pyridine." Molbank 2023, no. 2 (2023): M1613. http://dx.doi.org/10.3390/m1613.

Full text

Abstract:

As part of our ongoing antikinetoplastid structure–activity relationship study focused on positions 2 and 8 of the 3-nitroimidazo[1,2-a]pyridine scaffold, we were able to introduce a phenylthioether moiety at both position 2 and position 8 in one step. Using a previously reported synthetic route developed in our laboratory, we obtained 6-chloro-3-nitro-8-(phenylthio)-2-[(phenylthio)methyl]imidazo[1,2-a]pyridine in 74% yield. The in vitro cell viability of this compound was assessed on the HepG2 cell line, and its in vitro activity was evaluated against the promastigote form of L. donovani, the

APA, Harvard, Vancouver, ISO, and other styles

15

Sengoku, Tetsuya, Koki Makino, Ayumi Iijima, Toshiyasu Inuzuka та Hidemi Yoda. "Bifurcated synthesis of methylene-lactone- and methylene-lactam-fused spirolactams via electrophilic amide allylation of γ-phenylthio-functionalized γ-lactams". Beilstein Journal of Organic Chemistry 16 (13 листопада 2020): 2769–75. http://dx.doi.org/10.3762/bjoc.16.227.

Full text

Abstract:

New synthetic methods for spirolactams bearing an α-methylene-γ-butyrolactone or its analogous methylene-lactam have been developed. The allylation of γ-phenylthio-functionalized γ-lactams with 2-(acetoxy)methyl acrylamides was accomplished by using 2.5 equivalents of NaH to give the corresponding adducts in excellent yields. The remaining phenylthio group was substituted with a hydroxy group by treatment with CuBr, and the resulting γ-hydroxyamides were cyclized under acidic conditions to afford the corresponding methylene-lactam-fused spirolactams in high yields. On the other hand, methylene

APA, Harvard, Vancouver, ISO, and other styles

16

Bakuzis, Peter, and Marinalva L. F. Bakuzis. "Preparation of 1-(phenylthio)cyclopentenes and 1-(phenylthio)cyclohexenes by the Pummerer reaction." Journal of Organic Chemistry 50, no. 14 (1985): 2569–73. http://dx.doi.org/10.1021/jo00214a031.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Ashwell, Mark, Richard F. W. Jackson та Joanna M. Kirk. "Preparation of α-substituted S-phenylthio esters from 2-nitro-2-phenylthio oxiranes". Tetrahedron 46, № 21 (1990): 7429–42. http://dx.doi.org/10.1016/s0040-4020(01)89058-x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

LePichon, Luc, and Douglas W. Stephan. "Contrasting Formation of a (Phenylthio)phosphinimine and (Phenylthio)phosphazide. Synthesis of Metal Complexes." Inorganic Chemistry 40, no. 15 (2001): 3827–29. http://dx.doi.org/10.1021/ic001303x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

VILLA, M. J., and S. WARREN. "ChemInform Abstract: (1,4) Phenylthio Migrations in the Rearrangement of 2,4,4-Tris( phenylthio)butanols." ChemInform 26, no. 14 (2010): no. http://dx.doi.org/10.1002/chin.199514118.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Ghorai, Sujit K., Harendra N. Roy, Mousumi Bandopadhyay, and Dipakranjan Mal. "3-(Phenylthio)Phthalide: An Expedient Reagent in Phthalide Annulation." Journal of Chemical Research 23, no. 1 (1999): 30–31. http://dx.doi.org/10.1177/174751989902300121.

Full text

APA, Harvard, Vancouver, ISO, and other styles

21

Burford, N., B. W. Royan, and P. S. White. "Structure of tris(phenylthio)phosphine." Acta Crystallographica Section C Crystal Structure Communications 46, no. 2 (1990): 274–76. http://dx.doi.org/10.1107/s010827018900630x.

Full text

APA, Harvard, Vancouver, ISO, and other styles

22

Coldham, Iain, and Stuart Warren. "Stereocontrolled amidocyclisations with phenylthio migration." Tetrahedron Letters 30, no. 43 (1989): 5937–40. http://dx.doi.org/10.1016/s0040-4039(01)93510-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Feng, Liu, Weng-hua Zhang, Shuo-kui Han, Lian-Zheng Wang, and Zheng Zhang. "Hydrolysis kinetics of phenylthio-carboxylates." Chemosphere 32, no. 9 (1996): 1691–97. http://dx.doi.org/10.1016/0045-6535(96)00086-0.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Lozano, A. E., J. De Abajo, J. G. De La Campa, and J. Preston. "Polyisophthalamides with phenylthio pendent groups." Journal of Polymer Science Part A: Polymer Chemistry 30, no. 7 (1992): 1327–33. http://dx.doi.org/10.1002/pola.1992.080300710.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

Asali, Khalil J. "Bimetallic Group 6 Tricarbonyls Triply-Bridged by Bis(phenylthio)alkane Bidentate Ligands." Advanced Materials Research 93-94 (January 2010): 13–16. http://dx.doi.org/10.4028/www.scientific.net/amr.93-94.13.

Full text

Abstract:

Reactions of the labile complex (Me3tach)M(CO)3 (Me3tach = 1,3,5-trimethyl-1,3,5-triazacyclohexane; M = W, Mo) with bis(phenylthio)alkanes ( = PhS(CH2)nSPh), (2:3 molar ratio) in CH2Cl2 as solvent (at 35 oC M = W, 0 oC M = Mo) afforded in good yields bimetallic tricarbonyl complexes triply- bridged by bis(phenylthio)alkanes of the type [M(CO)3]2(μ-PhS-(CH2)n-SPh)3 [n = 3 (a), 4 (b), 5 (c), 6 (d); M = W (1), Mo (2)]. These new triply-bridged complexes were characterized by 1H NMR, FT-IR and elemental analysis. Additionally, it has been observed that the thermodynamic stability of some of these

APA, Harvard, Vancouver, ISO, and other styles

26

You, Fen, Hui Liu, Gen Luo, and Xiaochao Shi. "Tridentate diarylamido-based pincer complexes of nickel and palladium: sidearm effects in the polymerization of norbornene." Dalton Transactions 48, no. 32 (2019): 12219–27. http://dx.doi.org/10.1039/c9dt02361e.

Full text

Abstract:

The sidearm effects were found in the polymerization of norbornene catalyzed by the Ni and Pd complexes bearing new diarylamido based unsymmetrical quinolino [NNN<sup>ox</sup>] and phenylthio [SNN<sup>ox</sup>] pincer ligands.

APA, Harvard, Vancouver, ISO, and other styles

27

Zhu, Yao-Yao, Shuai Liu, Yangen Huang, Feng-Ling Qing, and Xiu-Hua Xu. "Photoredox catalyzed difluoro(phenylthio)methylation of 2,3-allenoic acids with {difluoro(phenylthio)methyl}triphenylphosphonium triflate." Journal of Fluorine Chemistry 257-258 (May 2022): 109969. http://dx.doi.org/10.1016/j.jfluchem.2022.109969.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Kwon, Tae Woo, and Michael B. Smith. "Preparation and Reactions of 1,1-Di(Phenylthio)Cyclobutane Derivatives from 1-(Phenylthio)-1-Cyclopropane Carbinols." Synthetic Communications 22, no. 15 (1992): 2273–85. http://dx.doi.org/10.1080/00397919208019081.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

ASHWELL, M., R. F. W. JACKSON та J. M. KIRK. "ChemInform Abstract: Preparation of α-Substituted S-Phenylthio Esters from 2-Nitro-2- phenylthio Oxiranes." ChemInform 22, № 8 (2010): no. http://dx.doi.org/10.1002/chin.199108145.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Prakash, G. K. Surya, Jinbo Hu, Ying Wang, and George A. Olah. "Fluoride-induced nucleophilic (phenylthio)difluoromethylation of carbonyl compounds with [difluoro(phenylthio)methyl]trimethylsilane (TMS–CF2SPh)." Journal of Fluorine Chemistry 126, no. 4 (2005): 527–32. http://dx.doi.org/10.1016/j.jfluchem.2004.12.005.

Full text

APA, Harvard, Vancouver, ISO, and other styles

31

Alhaj, N. M. I., A. M. Uduman Mohideen, and S. Sofia Lawrence Mary. "Mechanism of Oxidation of (p-Substituted Phenylthio)acetic Acids withN-Chlorosaccharin." E-Journal of Chemistry 8, no. 1 (2011): 159–66. http://dx.doi.org/10.1155/2011/342409.

Full text

Abstract:

The kinetics of oxidation of (phenylthio)acetic acid (PTAA) withN-chlorosaccharin (NCSA) have been studied potentiometrically in 80:20 (v/v) acetonitrile-water medium at 298 K. The reaction is first-order each with respect to PTAA and NCSA and shows a negative dependence on [H+]. NCSA itself is shown to be the active oxidizing species. Effects of ionic strength variation, added saccharin, added acrylonitrile, added NaCl and solvent composition variation have been studied. Effect of substituents on the reaction rate has been analysed by employing various (p-sustituted phenylthio)acetic acids. T

APA, Harvard, Vancouver, ISO, and other styles

32

Wu, Jingjing, Hui Li, and Song Cao. "Novel synthesis of pseudopeptides bearing a difluoromethyl group by Ugi reaction and desulfanylation." Beilstein Journal of Organic Chemistry 7 (August 8, 2011): 1070–74. http://dx.doi.org/10.3762/bjoc.7.123.

Full text

Abstract:

Thirteen difluoromethyl-containing pseudopeptides were synthesized by Ugi reaction using the novel building block 2,2-difluoro-2-(phenylthio)acetic acid (2) as one component, followed by removal of the phenylsulfanyl protecting group in the presence of tributyltin hydride and azobisisobutyronitrile.

APA, Harvard, Vancouver, ISO, and other styles

33

Verma, Chandrabhan, Lukman O. Olasunkanmi, I. B. Obot, Eno E. Ebenso, and M. A. Quraishi. "2,4-Diamino-5-(phenylthio)-5H-chromeno [2,3-b] pyridine-3-carbonitriles as green and effective corrosion inhibitors: gravimetric, electrochemical, surface morphology and theoretical studies." RSC Advances 6, no. 59 (2016): 53933–48. http://dx.doi.org/10.1039/c6ra04900a.

Full text

Abstract:

The inhibition of mild steel corrosion in 1 M HCl by three newly synthesized 2,4-diamino-5-(phenylthio)-5H-chromeno[2,3-b]pyridine-3-carbonitriles was studied using the weight loss method, electrochemical techniques, surface morphology studies and theoretical methods.

APA, Harvard, Vancouver, ISO, and other styles

34

Barlin, GB, LP Davies, PW Harrison, NW Jacobsen, and AC Willis. "Imidazo[1,2-b]Pyridazines. XVI. Synthesis and Central Nervous System Activities of Some 6-(Chloro, Alkylthio, Phenylthio, Benzylthio or Pyridinylmethylthio)-3-(unsubstituted, benzamidomethyl or methoxy)-2-(styryl or benzoyl)imidazo[1,2-b]pyridazines." Australian Journal of Chemistry 47, no. 11 (1994): 1989. http://dx.doi.org/10.1071/ch9941989.

Full text

Abstract:

Some 6-( chloro, alkylthio, phenylthio, benzylthio or pyridinylmethylthio )-3-( unsubstituted , benzamidomethyl or methoxy )-2-styrylimidazo[1,2-b] pyridazines and 6-chloro-3-( unsubstituted and benzamidomethyl )-2-benzoylimidazo[1,2-b] pyridazines have been prepared and tested for their ability to displace [3H]diazepam from rat brain plasma membranes. The structures of 6-chloro-2-benzoyl[and 6-fluoro-2-(4′-tolyl)] imidazo [1,2-b] pyridazine have been confirmed by X-ray analyses. The reactions of 6-methylthio(and 6-phenylthio)pyridazin-3-amines with 3-bromo-1-phenylpropane-1,2-dione also have

APA, Harvard, Vancouver, ISO, and other styles

35

Pang, L., F. Brisse, and E. A. C. Lucken. "Order–disorder effects in clathrates. A crystallographic and 35Cl NQR spectroscopic study of CCl3X guest molecules (X=Cl, Br, CH3, CN, NO2, H) in hexakis(phenylthio)benzene." Canadian Journal of Chemistry 73, no. 3 (1995): 351–61. http://dx.doi.org/10.1139/v95-047.

Full text

Abstract:

X-ray crystallography and NQR spectroscopy have been jointly used to study CCl3X-hexakis(phenylthio)benzene (HPTB) (X=Cl, Br, CH3, CN, NO2, H) clathrates. The crystal of the non-clathrated HPTB is triclinic, [Formula: see text] a = 9.5614(7), b = 10.2088(13), c = 10.6193(11) Å, α = 68.45(1)°, β = 76.98(1)°, γ = 65.62(1)°, Z = 1; crystals of the clathrates with CCl3CH3, CCl3Br, CCl3NO2, and CCl3CN are isostructural and trigonal, [Formula: see text] a = 14.18–14.32, c = 20.47–20.62 Å, Z = 3. The trigonal host cavity of HPTB clathrates contains two CCl3X guest molecules, and the X group occupies

APA, Harvard, Vancouver, ISO, and other styles

36

Saleem, Fariha, Gyandshwar K. Rao, Satyendra Kumar, Mahabir Pratap Singh та Ajai K. Singh. "Complexes of (η6-benzene)ruthenium(ii) with 1,4-bis(phenylthio/seleno-methyl)-1,2,3-triazoles: synthesis, structure and applications in catalytic activation of oxidation and transfer hydrogenation". Dalton Transactions 44, № 44 (2015): 19141–52. http://dx.doi.org/10.1039/c5dt02926k.

Full text

Abstract:

1,4-Bis(phenylthio/seleno methyl)-1,2,3-triazoles (L1–L4) synthesized by a ‘Click’ reaction form complexes [(η<sup>6</sup>-C<sub>6</sub>H<sub>6</sub>)RuClL]PF<sub>6</sub> (L = L1–L4) suitable as catalyst for oxidation/transfer hydrogenation.

APA, Harvard, Vancouver, ISO, and other styles

37

Ferguson, G., B. Kaitner, B. M. Dilworth, and M. A. McKervey. "Structure of 1,1,4,4-tetrakis(phenylthio)butane." Acta Crystallographica Section C Crystal Structure Communications 46, no. 8 (1990): 1540–42. http://dx.doi.org/10.1107/s0108270189013326.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Lynch, Daniel E., and Ian McClenaghan. "2-Amino-4,6-bis(phenylthio)pyrimidine." Acta Crystallographica Section E Structure Reports Online 57, no. 1 (2000): o26—o27. http://dx.doi.org/10.1107/s1600536800017888.

Full text

Abstract:

The structure of the title compound, C16H13N3S2, (I), consists of molecules that associateviaN—H...N and N—H...S interactions to form a linear one-dimensional hydrogen-bonded chain. The dihedral angles between the two phenyl rings and the pyrimidine ring are 74.94 (7) and 75.47 (7)°.

APA, Harvard, Vancouver, ISO, and other styles

39

Barrett, Anthony G. M., Gregory G. Graboski, Michal Sabat, and Sven J. Taylor. ".beta.-Lactam annulation using (phenylthio)nitromethane." Journal of Organic Chemistry 52, no. 21 (1987): 4693–702. http://dx.doi.org/10.1021/jo00230a008.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

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.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

41

Villa, María-Jesús, and Stuart Warren. "[1,4] Phenylthio shifts of 2,4,4-trisphenylthiobutanols." Tetrahedron Letters 30, no. 43 (1989): 5933–36. http://dx.doi.org/10.1016/s0040-4039(01)93509-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Shibao, R. K., N. L. Keder, and H. Eckert. "Structure of tris(phenylthio)phosphine sulfide." Acta Crystallographica Section C Crystal Structure Communications 48, no. 8 (1992): 1525–27. http://dx.doi.org/10.1107/s0108270191014919.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Esker, John L., and Martin Newcomb. "Amidyl radicals from N-(phenylthio)amides." Tetrahedron Letters 34, no. 43 (1993): 6877–80. http://dx.doi.org/10.1016/s0040-4039(00)91819-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Takano, Seiichi, Osamu Yamada, Hirokazu Lida, and Kunio Ogasawara. "Enantiocomplementary Resolution of 2-Phenylthio-2-cyclopentenol and 2-Phenylthio-2-cyclohexenol Using the Same Lipase." Synthesis 1994, no. 06 (1994): 592–96. http://dx.doi.org/10.1055/s-1994-25529.

Full text

APA, Harvard, Vancouver, ISO, and other styles

45

Maguire, Anita R., Maureen E. Murphy, Marcel Schaeffer, and George Ferguson. "Single step stereospecific transformation of 2-phenylthio secondary amides into (Z)-3-chloro-2-phenylthio acrylamides." Tetrahedron Letters 36, no. 3 (1995): 467–70. http://dx.doi.org/10.1016/0040-4039(94)02288-m.

Full text

APA, Harvard, Vancouver, ISO, and other styles

46

Han, Jianwei, Yanxia Zhang, Xin-Yan Wu, and Henry N. C. Wong. "Chiral iminophosphorane catalyzed asymmetric sulfenylation of 4-substituted pyrazolones." Chemical Communications 55, no. 3 (2019): 397–400. http://dx.doi.org/10.1039/c8cc09049a.

Full text

Abstract:

An excellent level of enantioselectivity in asymmetric sulfenylation of 4-substituted pyrazolones was achieved with chiral iminophosphorane as organocatalyst under the continuum solvation conditions. The use of hydrocarbon solvents enabled to enhance the enantiomeric excesses of the desired 4-phenylthio-pyrazol-5-ones (up to 99% ee).

APA, Harvard, Vancouver, ISO, and other styles

47

Reddy, B. V. Subba, S. Rehana Anjum, and B. Sridhar. "A novel self-terminated Prins strategy for the synthesis of tetrahydropyran-4-one derivatives and their behaviour in Fisher indole synthesis." RSC Advances 6, no. 79 (2016): 75133–37. http://dx.doi.org/10.1039/c6ra11218h.

Full text

Abstract:

A novel self-terminated Prins strategy has been developed for the synthesis of 2-substituted tetrahydropyran-4-one derivatives through a condensation of 3-(phenylthio)but-3-en-1-ol with carbonyl compounds in the presence of 5 mol% of Sc(OTf)<sub>3</sub> under mild conditions.

APA, Harvard, Vancouver, ISO, and other styles

48

Špirková, Katarína, Rudolf Kada, Jaroslav Kováč, Viera Knoppová, Miroslav Dzuroška, and Margita Margušová. "A study of reactions of 5-substituted furfurylidene derivatives with secondary amines." Collection of Czechoslovak Chemical Communications 50, no. 2 (1985): 459–69. http://dx.doi.org/10.1135/cccc19850459.

Full text

Abstract:

The paper describes preparation of 5-bromo-, 5-nitro-, 5-phenylsulphonyl-, and 5-phenylthio-2-furfurylidene derivatives and investigation of their reactions with N-phenylpiperazine, morpholine, piperidine, and pyrrolidine. Kinetics of the reactions have been followed, and UV, IR, and 1H NMR spectra of the compounds produced are interpreted.

APA, Harvard, Vancouver, ISO, and other styles

49

KWON, T. W., and M. B. SMITH. "ChemInform Abstract: Preparation and Reactions of 1,1-Di(phenylthio)cyclobutane Derivatives from 1-(Phenylthio)-1-cyclopropane Carbinols." ChemInform 24, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199307179.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Ramalingam, S., S. Perumal, S. Selvaraj, and S. Sivasubramanian. "ChemInform Abstract: Chemoselective Electrooxidation of (E)-1-Phenyl-2-(phenylthio)ethylene and 1-Phenyl-2-(phenylthio)acetylene." ChemInform 30, no. 40 (2010): no. http://dx.doi.org/10.1002/chin.199940083.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!