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2017
DOI: 10.1002/aoc.3869
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Eco‐compatible three component strategies for C‐S bond formation in thioether and S‐aryl‐carbamodithioate compounds catalyzed by copper(II) nanoparticles supported on modified AlPO4

Abstract: One‐pot and three components C‐S bond formation reactions in thioethers and S‐aryl‐carbamodithioates have been catalyzed by a copper heterogeneous nano‐catalyst supported on modified AlPO4 under different reaction conditions. The above‐mentioned nano‐catalyst has been characterized by various techniques such as SEM, TEM, AFM, XRD, FT‐IR, UV–Vis, CV, BET, TGA, ICP and XPS spectrometry and its particle size was estimated to be between 60–110 nm. Finally, the reusability of the catalyst up to ten cycles without a… Show more

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Cited by 7 publications
(10 citation statements)
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“…All known compounds were identified by comparison of their melting points and proton nuclear magnetic resonance ( 1 H NMR) data with those in the authentic samples. The 1 H NMR (250 MHz) and 13 C NMR (100 MHz) were run on a Bruker Avance DPX-250 and Bruker Avance DPX-400 fourier transform (FT)-NMR spectrometers respectively. Chemical shifts are given as δ values against tetramethylsilane (TMS) as the internal standard and J values are given in Hz.…”
Section: Methodsmentioning
confidence: 99%
See 3 more Smart Citations
“…All known compounds were identified by comparison of their melting points and proton nuclear magnetic resonance ( 1 H NMR) data with those in the authentic samples. The 1 H NMR (250 MHz) and 13 C NMR (100 MHz) were run on a Bruker Avance DPX-250 and Bruker Avance DPX-400 fourier transform (FT)-NMR spectrometers respectively. Chemical shifts are given as δ values against tetramethylsilane (TMS) as the internal standard and J values are given in Hz.…”
Section: Methodsmentioning
confidence: 99%
“…Isolated yield: 75% (0.19 g). Colorless liquid, 1 H NMR (250 MHz, CDCl 3 ): δ (ppm) 1.37 (s, 9H), 1.50 (s, 9H), 5.82 (d,J = 12.5 Hz,1H),6.43 (d,J = 17.5 Hz,1H),6.76 (dd,J = 17.5,10.0 Hz, 1H), 7.29 (s, 1H), 7.57 (s, 1H); 13 C{H} NMR (100 MHz, CDCl 3 ): δ (ppm) 30.0, 31. 8,34.4,35.1,114.3,119.9,124.2,124.4,133.7,141.9,147.7,161.6.…”
Section: 7-di-tert-butyl-2-undecylbenzo[d]oxazole (4 F)mentioning
confidence: 99%
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“…Tetrazoles are types of polyazaheterocyclic compounds . They have widespread applications in medicine, materials science and coordination chemistry . The [2 + 3] cycloaddition of azides to the corresponding nitriles in the presence of an appropriate catalyst is the best method for the synthesis of 5‐substituted 1 H ‐tetrazoles .…”
Section: Introductionmentioning
confidence: 99%