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1.
Org Lett ; 26(17): 3634-3639, 2024 May 03.
Artículo en Inglés | MEDLINE | ID: mdl-38660998

RESUMEN

In this paper, we report an unprecedented copper-catalyzed disulfides or sulfides coupling reaction involving unactivated alkyl halides and N-dithiophthalimides. This reaction can be conducted under mild conditions using low-cost metal catalysts and exhibits high chemical selectivity and functional group compatibility, enabling the efficient assembly of various sulfides and disulfides.

3.
Org Lett ; 22(16): 6600-6604, 2020 Aug 21.
Artículo en Inglés | MEDLINE | ID: mdl-32806158

RESUMEN

A diverse chemoselective insertion reaction of sulfoxonium ylides and thiosulfonates under transition-metal-free conditions is developed, which successfully affords 1,4-diketone compounds, arylthiosulfoxide-ylides, and ß-keto thiosulfones, respectively. The nucleophilic addition of two molecular sulfoxonium ylides to construct sulfone-substituted 1,4-dione compounds is the highlight of this work.

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