ArticleNature communications2020
Addition of alkynes and osmium carbynes towards functionalized d
Article in Nature communications, 2020. 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
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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
12 citing papers in PubMed.
- Metallacyclobutadienes: Intramolecular Rearrangement from Kinetic to Thermodynamic Isomers.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024Article
- Water-catalyzed iron-molybdenum carbyne formation in bimetallic acetylene transformation.Nature communications · 2024Article
- Syntheses and reactivities of strained fused-ring metallaaromatics containing planar eleven-carbon chains.Nature communications · 2024Article
- Rhenium Alkyne Catalysis: Sterics Control the Reactivity.Inorganic chemistry · 2024Article
- Phenanthroline-carbolong interface suppress chemical interactions with active layer enabling long-time stable organic solar cells.Nature communications · 2023Article
- Reshaping aromatic frameworks: expansion of aromatic system drives metallabenzenoids to metallapentalenes.Chemical science · 2023Article
- Synthesis and characterization of Craig-type antiaromatic species with [4Proceedings of the National Academy of Sciences of the United States of America · 2023Article
- Heterocyclic Suzuki-Miyaura coupling reaction of metalla-aromatics and mechanistic analysis of site selectivity.Chemical science · 2023Article
- Conjugated polymers based on metalla-aromatic building blocks.Proceedings of the National Academy of Sciences of the United States of America · 2022Article
- Direct amidation of metallaaromatics: access toChemical science · 2021Article
- Open questions on aromaticity in organometallics.Communications chemistry · 2020Article
- Recent Advances in the Reactions of Cyclic Carbynes.Molecules (Basel, Switzerland) · 2020Review
Corrections and comments
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Authors and funding
10 authors.
Funding
Abstract
The metal-carbon triple bonds and carbon-carbon triple bonds are both highly unsaturated bonds. As a result, their reactions tend to afford cycloaddition intermediates or products. Herein, we report a reaction of M≡C and C≡C bonds that affords acyclic addition products. These newly discovered reactions are highly efficient, regio- and stereospecific, with good functional group tolerance, and are robust under air at room temperature. The isotope labeling NMR experiments and theoretical calculations reveal the reaction mechanism. Employing these reactions, functionalized d
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.