2023
DOI: 10.1002/aoc.7132
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Ru@C as a safety mask of RuO4@C for selective catalytic oxidation of alkynyl sulfurs to prepare alkynylsulfones

Abstract: A high‐performance catalyst, RuO4@C, was safely generated in situ from a safety mask Ru@C, which was recyclable and commercially available. The catalyst could selectively oxidize thioethers to sulfones in 95%–99% yields and alkynyl sulfurs to alkynylsulfones in 93%–98% yields. This safe, non‐toxic, inexpensive, and readily available catalyst is potentially promising for industrial applications in the production of sulfones from sulfur oxidation.

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Cited by 2 publications
(1 citation statement)
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“…Within the realm of medicinal chemistry and pharmaceutical research, sulfones, particularly the alkynyl variants, play a crucial role due to their noteworthy pharmacological properties (Scheme 1a) [1] and versatility as synthetic intermediates in a range of chemical reactions like cycloadditions, conjugated additions, and cross-coupling reactions. [2] Traditional synthetic methodologies for alkynyl sulfones, incorporating the oxidation of alkynyl sulfides, [3] sulfonylation of alkynylsilanes or alkynylstannides, [4] and dehydrohalogenation of vinyl sulfones, [5] necessitate pre-functionalized substrates or elaborate multistep procedures. The evolution of CÀ S coupling reactions [6] employing sulfonyl radicals offers a more efficient and direct strategy for the synthesis of alkynyl sulfones.…”
Section: Introductionmentioning
confidence: 99%
“…Within the realm of medicinal chemistry and pharmaceutical research, sulfones, particularly the alkynyl variants, play a crucial role due to their noteworthy pharmacological properties (Scheme 1a) [1] and versatility as synthetic intermediates in a range of chemical reactions like cycloadditions, conjugated additions, and cross-coupling reactions. [2] Traditional synthetic methodologies for alkynyl sulfones, incorporating the oxidation of alkynyl sulfides, [3] sulfonylation of alkynylsilanes or alkynylstannides, [4] and dehydrohalogenation of vinyl sulfones, [5] necessitate pre-functionalized substrates or elaborate multistep procedures. The evolution of CÀ S coupling reactions [6] employing sulfonyl radicals offers a more efficient and direct strategy for the synthesis of alkynyl sulfones.…”
Section: Introductionmentioning
confidence: 99%