ArticleOrganic letters2020
Hexafluoroisopropanol-Promoted Disulfidation and Diselenation of Alkyne, Alkene, and Allene.
Article in Organic letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 39 citations in OpenAlex.
- Silylium-Ion-Initiated Disulfidation of Internal Alkynes With Disulfides.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026Article
- Oxidative rearrangement of alkynes to chiral α-arylalkanoic esters.Chemical science · 2026Article
- Tuning Selectivity in the Visible-Light-Promoted Coupling of Thiols with Alkenes by EDAACS omega · 2023Article
- Diphenyl Diselenide-Assisted Radical Addition Reaction of Diphenyl Disulfide to Unsaturated Bonds upon Photoirradiation.Molecules (Basel, Switzerland) · 2023Article
- Iodine-mediated oxythiolation ofRSC advances · 2022Article
- Anticancer-active 3,4-diarylthiolated maleimides synthesisFrontiers in chemistry · 2022Article
- ESI-MS Analysis of Thiol-yne Click Reaction in Petroleum Medium.Molecules (Basel, Switzerland) · 2021Article
Corrections and comments
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Authors and funding
6 authors at 2 institutions in 2 countries.
Funding
Abstract
Hexafluoroisopropanol (HFIP)-promoted disulfidation and diselenation of C-C unsaturated bonds is reported. Reactions of unactivated alkyne, alkene, and allene, respectively, with disulfides or diselenides in HFIP led to desired products in good to excellent yields (up to 96%). In contrast, other solvents, such as isopropanol and dichloroethane, could not promote the same reaction. This method revealed an example of HFIP-promoted transformations under the mild conditions, which greatly highlighted the unique reactivity of this special solvent.
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Registered trials
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