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Record W1522177818 · doi:10.1002/3527606548.ch1

Structure, Properties, and Preparation of Boronic Acid Derivatives. Overview of Their Reactions and Applications

2005· other· en· W1522177818 on OpenAlexaff
Dennis G. Hall

Bibliographic record

Venuenot available
Typeother
Languageen
FieldChemistry
TopicOrganoboron and organosilicon chemistry
Canadian institutionsUniversity of Alberta
Fundersnot available
KeywordsChemistryBoronic acidTransmetalationOrganic chemistryHydroborationArylSuzuki reactionRegioselectivityCombinatorial chemistryCatalysisAlkyl

Abstract

fetched live from OpenAlex

This chapter contains sections titled: Introduction Structure and Properties of Boronic Acid Derivatives General Types and Nomenclature of Boronic Acid Derivatives Boronic Acids Structure and Bonding Physical Properties and Handling Safety Considerations Acidic Character Chemical Stability Boronic Acid Derivatives Boroxines Boronic Esters Dialkoxyboranes and other Heterocyclic Boranes Diboronyl Esters Azaborolidines and other Boron Heterocycles Dihaloboranes and Monoalkylboranes Trifluoroborate Salts Synthesis of Boronic Acids and their Esters Arylboronic Acids Electrophilic Trapping of Arylmetal Intermediates with Borates Transmetallation of Aryl Silanes and Stannanes Coupling of Aryl Halides with Diboronyl Reagents Direct Boronylation by Transition Metal-catalyzed Aromatic C-H Functionalization Other Methods Diboronic Acids Heterocyclic Boronic Acids Alkenylboronic Acids Electrophilic Trapping of Alkenymetal Intermediates with Borates Transmetallation Methods Transition-metal Catalyzed Coupling between Alkenyl Halides/Triflates and Diboronyl Reagents Hydroboration of Alkynes Alkene Metathesis Other Methods Alkynylboronic Acids Alkylboronic Acids Allylic Boronic Acids Chemoselective Transformations of Compounds containing a Boronic Acid (Ester)- Substituent Oxidative Methods Reductive Methods Generation and Reactions of α-Boronyl-substituted Carbanions and Radicals Reactions of (α-Haloalkyl)boronic Esters Other Transformations Isolation and Characterization Chromatography and Recrystallization Solid Supports for Boronic Acid Immobilization and Purification Diethanolaminomethyl Polystyrene Other Solid-supported Diol Resins Soluble Diol Approaches Analytical and Spectroscopic Methods for Boronic Acid Derivatives Melting Points and Combustion Analysis Mass Spectrometry Nuclear Magnetic Resonance Spectroscopy Other Spectroscopic Methods Overview of the Reactions of Boronic Acid Derivatives Metallation and Metal-catalyzed Protodeboronation Oxidative Replacement of Boron Oxygenation Amination Halogenation Carbon–Carbon Bond forming Processes Palladium-catalyzed Cross-coupling with Carbon Halides (Suzuki Coupling) Allylation of Carbonyl Compounds Uncatalyzed Additions to Imines and Iminiums Rhodium-catalyzed Additions to Aldehydes and Alkenes Heck-type Coupling to Alkenes and Alkynes Carbon–Heteroatom Bond forming Processes Copper-catalyzed Coupling with Nucleophilic Oxygen and Nitrogen-containing - Compounds Other Reactions Overview of other Applications of Boronic Acid Derivatives Use as Reaction Promoters and Catalysts Use as Protecting Groups for Diols and Diamines Use as Supports for Derivatization and Affinity Purification of Diols, Sugars, and Glycosylated Proteins Use as Receptors and Sensors for Carbohydrates and other Small Molecules Use as Antimicrobial Agents and Enzyme Inhibitors Use in Neutron Capture Therapy for Cancer Use in Transmembrane Transport Use in Bioconjugation and Labeling of Proteins and Cell Surface References

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Other · Consensus signal: none
Teacher disagreement score0.619
Threshold uncertainty score0.992

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0080.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.023
GPT teacher head0.261
Teacher spread0.239 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designBench or experimental
Domainnot available
GenreOther

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations188
Published2005
Admission routes1
Has abstractyes

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