ArticleAngewandte Chemie (International ed. in English)2021
C-Boron Enolates Enable Palladium Catalyzed Carboboration of Internal 1,3-Enynes.
Article in Angewandte Chemie (International ed. in English), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 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.
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Who cites it
9 citing papers in PubMed.
- Synthesis and Characterization of anInorganic chemistry · 2026Article
- Metal π-Lewis base activation in palladium(0)-catalyzedChemical science · 2024Article
- Borataalkenes, boraalkenes, and the ηChemical Society reviews · 2024Review
- Iterative Dual-Metal and Energy Transfer Catalysis Enables Stereodivergence in Alkyne Difunctionalization: Carboboration as Case Study.ACS catalysis · 2023Article
- Asymmetric Friedel-Crafts reaction of unsaturated carbonyl-tethered heteroarenesChemical science · 2023Article
- Synthesis of Allenes by Hydroalkylation of 1,3-Enynes with Ketones Enabled by Cooperative Catalysis.Journal of the American Chemical Society · 2023Article
- Article
- AChemical science · 2023Article
- Mechanism of Pd/Senphos-CatalyzedThe Journal of organic chemistry · 2023Article
Corrections and comments
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Authors and funding
8 authors.
Funding
Abstract
A new family of carbon-bound boron enolates, generated by a kinetically controlled halogen exchange between chlorocatecholborane and silylketene acetals, is described. These C-boron enolates are demonstrated to activate 1,3-enyne substrates in the presence of a Pd
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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.