2015
DOI: 10.1080/10426507.2015.1024311
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Transition-Metal-Free C–S Bond Formation: Aqueous Synthesis of S-Aryl Dithiocarbamates by The use of Stable Arenediazonium Salts Mediated by Nano-Magnetic Supported Silica Sulfonic Acid

Abstract: A convenient and transition-metal-free method for the synthesis of S-aryl dithiocarbamates based on the reaction of stable arenediazonium nano-magneto silica sulfates (ArN 2 + -OSO 3 -SiO 2 @Fe 3 O 4 ) with dithiocarbamic acid at room temperature was studied. Avoiding the use of any hazardous transition metal, simple procedure, low cast and short reaction time are noteworthy advantages of this methodology.

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Cited by 16 publications
(2 citation statements)
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References 37 publications
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“…The reaction is compatible with functional groups such as I, NO 2 , and COMe in the arenediazonium salts. The Nemati group 24b designed a similar C–S coupling, employing stable arenediazonium nano-magneto silica sulfates (ArN 2+ -OSO 3 -SiO 2 @Fe 3 O 4 ) as diazonium salts with water as the solvent.…”
Section: Reactions With Electrophilesmentioning
confidence: 99%
“…The reaction is compatible with functional groups such as I, NO 2 , and COMe in the arenediazonium salts. The Nemati group 24b designed a similar C–S coupling, employing stable arenediazonium nano-magneto silica sulfates (ArN 2+ -OSO 3 -SiO 2 @Fe 3 O 4 ) as diazonium salts with water as the solvent.…”
Section: Reactions With Electrophilesmentioning
confidence: 99%
“…Further SNAr reaction between the acid and diazonium salt leads to final product. F. Nemati group used a similar procedure for arenediazonium sulfates immobilized on magnetic nanoparticles as substrates (ArN 2 + -O3S-SiO2@Fe3O4) [38].…”
Section: C-chalcogens Bond Formationmentioning
confidence: 99%