ReviewRSC advances2025
Direct vicinal sulfonyloximation of alkenes: an efficient and straightforward approach towards the synthesis of α-sulfonyl ketoximes.
Review in RSC advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Direct vicinal halo-nitration of unsaturated compounds: an overview.RSC advances · 2025Review
Corrections and comments
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Direct vicinal sulfonylative difunctionalization of simple alkenes represents a powerful strategy for the rapid assembly of β-functionalized sulfones from simple starting materials. In this context, the direct sulfonyloximation of alkene substrates has recently received much attention from the chemical community owing to important applications of α-sulfonyl ketoxime products in organic synthesis. This review provides an overview of recent research on the titled reactions, with an emphasis on the reaction patterns and mechanisms. Literature has been surveyed until the end of 2024.
Identifiers
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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.