ArticleOrganic letters2014
DABSO-based, three-component, one-pot sulfone synthesis.
Article in Organic letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
24 citing papers in PubMed, 206 citations in OpenAlex.
- Sulfone-quinone derivatives: a review on their synthetic methods, properties and applications.RSC advances · 2026Review
- Regiodivergent sulfonylation of terminal olefinsNew journal of chemistry = Nouveau journal de chimie · 2023Article
- Tricomponent Decarboxysulfonylative Cross-Coupling Facilitates Direct Construction of Aryl Sulfones and Reveals a Mechanistic Dualism in the Acridine/Copper Photocatalytic System.ACS catalysis · 2022Article
- Visible-light-induced one-pot synthesis of sulfonic estersRSC advances · 2022Article
- Functional group divergence and the structural basis of acridine photocatalysis revealed by direct decarboxysulfonylation.Chemical science · 2022Article
- Chloroaluminate Ionic Liquid Immobilized on Magnetic Nanoparticles as a Heterogeneous Lewis Acidic Catalyst for the Friedel-Crafts Sulfonylation of Aromatic Compounds.Molecules (Basel, Switzerland) · 2022Article
- Recent Progress and Emerging Technologies towards a Sustainable Synthesis of Sulfones.ChemSusChem · 2021Review
- Base-Activated Latent Heteroaromatic Sulfinates as Nucleophilic Coupling Partners in Palladium-Catalyzed Cross-Coupling Reactions.Angewandte Chemie (International ed. in English) · 2021Article
- Divergent reactivity of sulfinates with pyridinium salts based on one-Chemical science · 2021Article
- Site-Selective C-H Functionalization-Sulfination Sequence to Access Aryl Sulfonamides.Organic letters · 2020Article
- Sulfinamide Synthesis Using Organometallic Reagents, DABSO, and Amines.The Journal of organic chemistry · 2020Article
- Cyclic Alkenylsulfonyl Fluorides: Palladium-Catalyzed Synthesis and Functionalization of Compact Multifunctional Reagents.Angewandte Chemie (International ed. in English) · 2019Article
- Bond-Forming and -Breaking Reactions at Sulfur(IV): Sulfoxides, Sulfonium Salts, Sulfur Ylides, and Sulfinate Salts.Chemical reviews · 2019Article
- Formation of an unexpected 3,3-diphenyl-3Beilstein journal of organic chemistry · 2019Article
- Engaging sulfinate saltsChemical science · 2018Article
- Direct sulfonylation of anilines mediated by visible light.Chemical science · 2018Article
- Copper(i)-catalyzed sulfonylative Suzuki-Miyaura cross-coupling.Chemical science · 2017Article
- One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromides.Chemical science · 2017Article
- Palladium(II)-Catalyzed Synthesis of Sulfinates from Boronic Acids and DABSO: A Redox-Neutral, Phosphine-Free Transformation.Angewandte Chemie (International ed. in English) · 2016Article
- Alkyl Sulfinates: Formal Nucleophiles for Synthesizing TosMIC Analogs.European journal of organic chemistry · 2015Article
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The addition of Grignard reagents or organolithium reagents to the SO2-surrogate DABSO generates a diverse set of metal sulfinates, suitable for direct conversion to sulfone products. The metal sulfinates can be trapped in situ with a wide range of C-electrophiles, including alkyl, allyl, and benzyl halides, epoxides, and (hetero)aryliodoniums.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.