ReviewMolecular diversity2025
Ring opening of epoxides: a facile approach towards the synthesis of polyketides and related stereoenriched natural products: a review.
Review in Molecular diversity, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 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
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Who cites it
3 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
- Photochemical synthesis of oxiranes using DABSO-activated sulfinates and allylic peroxides.Nature communications · 2026Article
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
Epoxides are significant heterocycles in the structural makeup of a variety of natural products. Their ring-opening reactions have emerged as a versatile and efficient strategies for synthesizing a variety of functionalized molecules. Such reactions have been extensively applied towards the preparation of complex naturally occurring products. The focus on epoxide ring-opening reactions within the scientific community has been increased, influenced by the goal to understand the synthesis of compounds that are important for their biological and structural significance. In this article, we have provided a concise account on the applications of epoxide's ring cleavage towards the syntheses of polyketides and related naturally occurring compounds, documented since last decade (2014-2023).
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39652268What 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.