ReviewMolecules (Basel, Switzerland)2013
Oxetane synthesis through the Paternò-Büchi reaction.
Review in Molecules (Basel, Switzerland), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 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
18 citing papers in PubMed.
- Photokinetics of Bimolecular Reactions: Predictive Modelling of the Basic Bimolecular Photoreactions XXYY'(Φ,k) and XX'YY'(Φ,k).Molecules (Basel, Switzerland) · 2026Article
- [2+2] Photocycloaddition reactions of sulfinylamines with alkenes to access β-sultam derivatives.Nature chemistry · 2026Article
- Photochemical Cyclization of Tertiary Buta-2,3-dienamides to β-Lactams Upon Triplet Energy Transfer.Angewandte Chemie (International ed. in English) · 2026Article
- Dearomatization of Aromatic Carbonyl Compounds by Photocycloaddition Reactions to 1,1-Dimethylallene.Organic letters · 2026Article
- Synthetic Approaches and Biological Significance of Four-membered Heterocyclic Compounds.Current topics in medicinal chemistry · 2026Review
- Photokinetics of Bimolecular Reactions: Analytically Solvable Rate Laws.Molecules (Basel, Switzerland) · 2025Article
- Oxetane Cleavage Pathways in the Excited State: Photochemical Kinetic Resolution as an Approach to Enantiopure Oxetanes.Journal of the American Chemical Society · 2025Article
- Oxetane-, Azetidine-, and Bicyclopentane-BearingOrganic letters · 2023Article
- Oxetane Synthesis via Alcohol C-H Functionalization.Journal of the American Chemical Society · 2023Article
- Chiral α-Stereogenic Oxetanols and AzetidinolsACS catalysis · 2022Article
- Enantioselective Iridium-Catalyzed Reductive Coupling of Dienes with Oxetanones and N-Acyl-Azetidinones Mediated by 2-Propanol.Angewandte Chemie (International ed. in English) · 2022Article
- Light-Triggered Click Chemistry.Chemical reviews · 2021Review
- Strain Release Chemistry of Photogenerated Small-Ring Intermediates.Chemistry (Weinheim an der Bergstrasse, Germany) · 2021Review
- Facile UV-induced covalent modification and crosslinking of styrene-isoprene-styrene copolymerRSC advances · 2021Article
- Synthesis of azetidines by aza Paternò-Büchi reactions.Chemical science · 2020Review
- A Photochemical Route to Optically Active Hexahydro-4The Journal of organic chemistry · 2019Article
- Enantioselective Synthesis of Oxetanes Bearing All-Carbon Quaternary Stereocenters via Iridium-Catalyzed C-C Bond-Forming Transfer Hydrogenation.Chemistry (Weinheim an der Bergstrasse, Germany) · 2017Article
- Photochemical Approaches to Complex Chemotypes: Applications in Natural Product Synthesis.Chemical reviews · 2016Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The Paternò-Büchi reaction is a photochemical reaction between a carbonyl compound and an alkene to give the corresponding oxetane. In this review the mechanism of the reaction is discussed. On this basis the described use in the reaction with electron rich alkenes (enolethers, enol esters, enol silyl ethers, enanines, heterocyclic compounds has been reported. The stereochemical behavior of the reaction is particularly stressed. We pointed out the reported applications of this reaction to the synthesis of naturally occuring compounds.
Indexed as
Identifiers
What 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.