ArticleOrganic & biomolecular chemistry2016
The Bull-James assembly as a chiral auxiliary and shift reagent in kinetic resolution of alkyne amines by the CuAAC reaction.
Article in Organic & biomolecular chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 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.
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Who cites it
8 citing papers in PubMed.
- Enantioselective copper-catalyzed azidation/click cascade reaction for access to chiral 1,2,3-triazoles.Nature communications · 2024Article
- A Colorimetric Method for Quantifying Cis and Trans Alkenes Using an Indicator Displacement Assay.Angewandte Chemie (International ed. in English) · 2021Article
- High-throughput assay for determining enantiomeric excess of chiral diols, amino alcohols, and amines and for direct asymmetric reaction screening.Nature protocols · 2020Article
- Coetaneous catalytic kinetic resolution of alkynes and azides through asymmetric triazole formation.Scientific reports · 2019Article
- Kinetic Resolution of Cyclic Secondary Azides, Using an Enantioselective Copper-Catalyzed Azide-Alkyne Cycloaddition.Organic letters · 2019Article
- Tetrafluoropyridyl (TFP): a general phenol protecting group readily cleaved under mild conditions.Organic & biomolecular chemistry · 2019Article
- Phosphino-Triazole Ligands for Palladium-Catalyzed Cross-Coupling.Organometallics · 2018Article
- Rigid and concave, 2,4-cis-substituted azetidine derivatives: A platform for asymmetric catalysis.Scientific reports · 2018Article
Corrections and comments
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Authors and funding
7 authors.
Funding
Abstract
The Bull-James boronic acid assembly is used simultaneously as a chiral auxiliary for kinetic resolution and as a chiral shift reagent for in situ enantiomeric excess (ee) determination by
Identifiers
What 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.