ArticleAngewandte Chemie (International ed. in English)2018
Enantioselective Construction of Tertiary Boronic Esters by Conjunctive Cross-Coupling.
Article in Angewandte Chemie (International ed. in English), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 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
29 citing papers in PubMed.
- Enabling sulfur-centered nucleophiles in conjunctive coupling: triethylborane-mediated trifluoromethylationChemical science · 2026Article
- Nickel-Catalyzed Boron-Mediated Saturative Trifunctionalization of Alkynes.Angewandte Chemie (International ed. in English) · 2026Article
- The current utility and future potential of multiborylated alkanes.Nature reviews. Chemistry · 2024Review
- Decarboxylation of β-boryl NHPI esters enables radical 1,2-boron shift for the assembly of versatile organoborons.Nature communications · 2023Article
- Iridium-Catalyzed Asymmetric Difunctionalization of C-C σ-Bonds Enabled by Ring-Strained Boronate Complexes.Journal of the American Chemical Society · 2023Article
- Enantioselective Construction of Carbocyclic and Heterocyclic Tertiary Boronic Esters by Conjunctive Cross-Coupling Reaction.Journal of the American Chemical Society · 2023Article
- Diastereoselective Alkylation of Activated Nitrogen Heterocycles with Alkenyl Boronate Complexes.Angewandte Chemie (International ed. in English) · 2023Article
- Palladium-Catalyzed Conjunctive Cross-Coupling with Electronically Asymmetric Ligands.The Journal of organic chemistry · 2023Article
- Annulative coupling of vinylboronic esters: aryne-triggered 1,2-metallate rearrangement.Chemical science · 2022Article
- Enantioselective Synthesis of Tertiary β-Boryl Amides by Conjunctive Cross-Coupling of Alkenyl Boronates and Carbamoyl Chlorides.Angewandte Chemie (International ed. in English) · 2022Article
- Three-component 1,2-carboamination of vinyl boronic estersChemical science · 2021Article
- Stereodivergent Access to Trisubstituted Alkenylboronate Esters through Alkene Isomerization.Organic letters · 2021Article
- Stereospecific 1,2-Migrations of Boronate Complexes Induced by Electrophiles.Angewandte Chemie (International ed. in English) · 2020Review
- Synthesis of 1,3-Bis-(boryl)alkanes through Boronic Ester Induced Consecutive Double 1,2-Migration.Angewandte Chemie (International ed. in English) · 2020Article
- Diastereo- and Enantioselective 1,4-Difunctionalization of Borylenynes by Catalytic Conjunctive Cross-Coupling.Angewandte Chemie (International ed. in English) · 2020Article
- Radical-Induced 1,2-Migrations of Boron Ate Complexes.Advanced synthesis & catalysis · 2020Review
- Catalytic Enantioselective Synthesis of anti-Vicinal Silylboronates by Conjunctive Cross-Coupling.Angewandte Chemie (International ed. in English) · 2020Article
- Asymmetric Hydrogenation of Unfunctionalized Tetrasubstituted Acyclic Olefins.Angewandte Chemie (International ed. in English) · 2020Article
- Alkyl Group Migration in Ni-Catalyzed Conjunctive Coupling with C(spOrganic letters · 2020Article
- Catalytic Enantioselective Synthesis of β-Allenyl Boronic Esters by Conjunctive Cross-Coupling with Propargylic Carbonates.ACS catalysis · 2019Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Catalytic enantioselective conjunctive cross-coupling has been developed to construct tertiary alkylboronic esters. These reactions occur with good yield and enantioselectivity for a range of substrates. Mechanistic experiments reveal aspects of the catalytic cycle that allow hindered substrates to react without significant complicating side reactions.
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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.