2009
DOI: 10.1002/chin.200930033
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ChemInform Abstract: CuO Nanoparticles Catalyzed C—N, C—O, and C—S Cross‐Coupling Reactions: Scope and Mechanism.

Abstract: Substitution reactions O 0040CuO Nanoparticles Catalyzed C-N, C-O, and C-S Cross-Coupling Reactions: Scope and Mechanism. -The reactions allow simple, general, and efficient access to a wide range of aromatic amines, phenol ethers, and thioethers. -(JAMMI, S.; SAKTHIVEL, S.; ROUT, L.; MUKHERJEE, T.; MANDAL, S.; MITRA, R.; SAHA, P.; PUNNIYAMURTHY*, T.; J.

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“…Aromatic carbons of lignin showed a very low signal between 102-156 ppm compared to C10-C16 aliphatic carbons. NMR signals of etherified lignin samples reflected previously reported O-alkyl phenolic compounds and thus further confirmed the successful etherification of lignin [45,46], as suggested also by high solubility in low-polarity solvents, such as chloroform and diethylether. In 13 C NMR spectra, the methyl carbon of C10-C16 chain units appeared around 14.4 ppm (Figure 4).…”
Section: Characterization Of Ligninssupporting
confidence: 83%
“…Aromatic carbons of lignin showed a very low signal between 102-156 ppm compared to C10-C16 aliphatic carbons. NMR signals of etherified lignin samples reflected previously reported O-alkyl phenolic compounds and thus further confirmed the successful etherification of lignin [45,46], as suggested also by high solubility in low-polarity solvents, such as chloroform and diethylether. In 13 C NMR spectra, the methyl carbon of C10-C16 chain units appeared around 14.4 ppm (Figure 4).…”
Section: Characterization Of Ligninssupporting
confidence: 83%
“…Another flamboyant category of EAOC is 'organo click reactions' in which electron-rich olefins such as enamines generated in situ would be treated with azides in the presence of organo catalysts such as secondary or tertiary amines. 37 In continuation of our previous contributions in azideolefin cycloaddition of electron-deficient olefins and organic azides using CuO nanoparticles, [38][39][40][41] we were prompted to examine the azide-olefin cycloaddition on bromoalkenes and organic azides. Our literature perusal on this aspect revealed the palladium-catalyzed synthesis of 1H -1,2,3-triazoles from sodium azide and alkenyl bromides (Eq.…”
Section: * For Correspondencementioning
confidence: 99%