ReviewNature reviews. Chemistry2026
Methods and applications for epoxide C-C bond cleavage reactions.
Review in Nature reviews. Chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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
2 citing papers in PubMed.
- Decarboxylative epoxidation of carboxylic acids for accelerating synthesis of oxiranes and derivatives.Nature communications · 2026Article
- Photoinduced deacylative epoxidation of ketone derivatives with allylic peroxides.Chemical science · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Epoxides are ubiquitous synthetic building blocks owing to the numerous tactics for their C-O bond cleavage. Remarkably, epoxides also undergo selective C-C bond cleavage by a broad range of transformations, utilizing orthogonal conditions to override the conventional C-O bond scission. These strategies allow the construction of diverse oxygenated cyclic and acyclic molecular backbones, often challenging to access otherwise. Here, we discuss the various modes of epoxide C-C bond cleavage reactions, highlighting synthetic applications of these reactions and suggesting directions for the further development of these powerful, yet underutilized, methods.
Identifiers
41326826What OpenQuestion holds
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.