23837-25-4Relevant academic research and scientific papers
Copper-catalyzed synthesis of sulfenamides utilizing diaryl disulfides with alkyl amines
Taniguchi, Nobukazu
, p. 1917 - 1920 (2007)
The copper-catalyzed coupling of diaryl disulfides with alkyl amines can afford various sulfenamides in good yields. Furthermore, the present reaction is efficient and can be used for both of the aryl sulfide groups on disulfide. Georg Thieme Verlag Stutt
The aqueous phase is generated in the catalytic molecular oxygen with S - N key of the sulfenamide compounds (by machine translation)
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Paragraph 0028, (2017/08/29)
The invention provides a water-phase catalytic molecular oxygen generation has S - N key of the sulfenamide compounds, in order to water-soluble transition metal phthalocyanine compound as a catalyst, in oxygen or in the air environment, the mercapto comp
Copper-catalyzed formation of sulfur-nitrogen bonds by dehydrocoupling of thiols with amines
Taniguchi, Nobukazu
experimental part, p. 2670 - 2673 (2010/07/18)
Copper-catalyzed formation of sulfur-nitrogen bonds can be performed by a dehydrocoupling of aryl thiols with amines. Sulfenamides or sulfonamides can be produced by the use of a copper catalyst in air or under oxygen atmosphere. Furthermore, a reaction involving the combination of a palladium catalyst and a copper catalyst selectively afforded sulfinamides.
