ArticleNature chemistry2016
Click chemistry: Straining to react.
Article in Nature chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 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
12 citing papers in PubMed.
- Lewis acid-catalyzed diastereoselective formal ene reaction of thioindolinones/thiolactams with bicyclobutanes.Chemical science · 2024Article
- Rhodium(I)-Catalyzed Annulation of Bicyclo[1.1.0]butyl-Substituted Dihydroquinolines and Dihydropyridines.Journal of the American Chemical Society · 2024Article
- Synthesis of Stereodefined Polysubstituted Bicyclo[1.1.0]butanes.Journal of the American Chemical Society · 2024Article
- From molecules to medicine: thiol selective bioconjugation in synthesis of diagnostic and therapeutic radiopharmaceuticals.Theranostics · 2024Review
- Lewis acid-catalyzed diastereoselective carbofunctionalization of bicyclobutanes employing naphthols.Chemical science · 2023Article
- How mono- and diphosphine ligands alter regioselectivity of the Rh-catalyzed annulative cleavage of bicyclo[1.1.0]butanes.Nature communications · 2022Article
- Bicyclobutanes: from curiosities to versatile reagents and covalent warheads.Chemical science · 2022Review
- The emerging role of radical chemistry in the amination transformation of highly strained [1.1.1]propellane: Bicyclo[1.1.1]pentylamine as bioisosteres of anilines.Frontiers in chemistry · 2022Review
- A Neutral Three-Membered 2π Aromatic Disilaborirane and the Unique Conversion into a Four-Membered BSiAngewandte Chemie (International ed. in English) · 2020Article
- Rationalizing the diverse reactivity of [1.1.1]propellane through σ-π-delocalization.Chemical science · 2020Article
- Strain-Release Heteroatom Functionalization: Development, Scope, and Stereospecificity.Journal of the American Chemical Society · 2017Article
- Eight-Step Enantioselective Total Synthesis of (-)-Cycloclavine.Angewandte Chemie (International ed. in English) · 2017Article
Corrections and comments
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
27001724What 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.