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Single-Molecule Interconversion between Chiral Configurations of Boronate Esters Observed in a Nanoreactor

https://doi.org/10.1021/acsnano.2c11286
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Kinetics of a Reversible Covalent-Bond-Forming Reaction Observed at the Single-Molecule Level
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Single‐Molecule Determination of the Isomers of d ‐Glucose and d ‐Fructose that Bind to Boronic Acids
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Single‐Molecule Observation of Intermediates in Bioorthogonal 2‐Cyanobenzothiazole Chemistry
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Kinetics of a Three‐Step Reaction Observed at the Single‐Molecule Level
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Single‐Molecule Covalent Chemistry with Spatially Separated Reactants
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Boronic Acids as Bioorthogonal Probes for Site‐Selective Labeling of Proteins
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Universal Reaction Mechanism of Boronic Acids with Diols in Aqueous Solution: Kinetics and the Basic Concept of a Conditional Formation Constant
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The stereodynamics of 1,2‐dipropyldiaziridines
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Time-resolved cryogenic modulation reveals isomer interconversion profiles in dynamic chromatography
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inferredcites →https://doi.org/10.1038/nnano.2014.264openalex-snapshot
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inferredcites →https://doi.org/10.1039/c8ra04503hopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c9sc05260gopenalex-snapshot
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inferredcites →https://doi.org/10.1039/d0cp05671eopenalex-snapshot
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inferredcites →https://doi.org/10.1073/pnas.1510565112openalex-snapshot
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inferredcites →https://doi.org/10.1111/cns.13190openalex-snapshot
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inferredcites →https://doi.org/10.1126/science.1144366openalex-snapshot
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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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