ArticleJournal of the American Chemical Society2019
Catalytic, Enantioselective
Article in Journal of the American Chemical Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 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
30 citing papers in PubMed.
- Selenium atom transfer enables selective bridged alkene-arylamine cycloaddition.Nature communications · 2026Article
- Synergistic diselenide/guanidine catalyzed dehydrophosphorylation of 2-nitrobenzhydrols to access C-stereogenic phosphinates.Chemical science · 2026Article
- Efficient synthesis of chiral vicinal diamines with four contiguous stereocenters via sequential dynamic kinetic resolution of 2,3-diamino-1,4-diketones.Nature communications · 2026Article
- A planar chiral organoselenium enabled enantioselective intramolecular oxidation of trisubstituted olefins.Nature communications · 2025Article
- Article
- Asymmetric Migratory Tsuji-Wacker Oxidation Enables the Enantioselective Synthesis of Hetero- and Isosteric Diarylmethanes.Journal of the American Chemical Society · 2024Article
- Asymmetric Synthesis of 2-Arylethylamines: A Metal-Free Review of the New Millennium.Molecules (Basel, Switzerland) · 2024Review
- Dynamic amine sorting enables multiselective construction of unsymmetrical chiral diamines.Nature chemistry · 2024Article
- Azocarboxamide-enabled enantioselective regiodivergent unsymmetrical 1,2-diaminations.Nature communications · 2024Article
- Incorporating azaheterocycle functionality in intramolecular aerobic, copper-catalyzed aminooxygenation of alkenes.RSC advances · 2024Article
- Intermolecular Aza-Wacker Coupling of Alkenes with Azoles by Photo-Aerobic Selenium-π-Acid Multicatalysis.ACS catalysis · 2024Article
- Catalytic 1,1-diazidation of alkenes.Nature communications · 2024Article
- Asymmetric Photoaerobic Lactonization and Aza-Wacker Cyclization of Alkenes Enabled by Ternary Selenium-Sulfur Multicatalysis.ACS catalysis · 2023Article
- Ring Opening of Aziridines by Pendant Sulfamates Allows for Regioselective and Stereospecific Preparation of Vicinal Diamines.The Journal of organic chemistry · 2023Article
- Recent Advances in the Use of Diorganyl Diselenides as Versatile Catalysts.Molecules (Basel, Switzerland) · 2023Review
- [3 + 2] Cycloadditions of Tertiary AmineOrganic letters · 2023Article
- Modular and practical diamination of allenes.Nature communications · 2023Article
- Hydrogen-Bond-Modulated Nucleofugality of SeAngewandte Chemie (International ed. in English) · 2022Article
- 1,2-Amino oxygenation of alkenes with hydrogen evolution reaction.Nature communications · 2022Article
- Enantioselective 1,3-Dipolar Cycloaddition Using (Molecules (Basel, Switzerland) · 2022Article
Corrections and comments
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Authors and funding
3 authors.
Funding
Abstract
The enantioselective, vicinal diamination of alkenes represents one of the stereocontrolled additions that remains an outstanding challenge in organic synthesis. A general solution to this problem would enable the efficient and selective preparation of widely useful, enantioenriched diamines for applications in medicinal chemistry and catalysis. In this article, we describe the first enantioselective,
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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.