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2005, ISBN 9783527309917, xxv, 549
Dennis Hall is a Professor of Chemistry at the University of Alberta (Edmonton, Canada). He was born in 1968 in northern Quebec, Canada, and was educated at... 
Synthesis | Organoboron compounds | Organic acids | Therapeutic use
Book
Advanced Synthesis & Catalysis, ISSN 1615-4150, 02/2015, Volume 357, Issue 2‐3, pp. 474 - 480
Journal Article
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 01/2015, Volume 56, Issue 1, pp. 172 - 174
A metal free, mild, and highly efficient methodology for -hydroxylation of diversely functionalized aryl- and alkylboronic acids/esters mediated by iodobenzene... 
Aliphatic alcohols | Hydroxylation | Hypervalent iodine, DAIB | Organoboronic acids/esters | Aromatic alcohols | CHEMISTRY, ORGANIC | ARYLBORONIC ACIDS | BORONIC ACIDS | MILD | CROSS-COUPLING REACTIONS | PHENOLS | OXIDATIVE HYDROXYLATION | ESTERS | Tetrahedrons | Esters | Methodology | Nucleophiles | Ambient temperature
Journal Article
Chemical Communications, ISSN 1359-7345, 2018, Volume 54, Issue 43, pp. 5410 - 5413
2,4-Bis(trifluoromethyl) phenylboronic acid is a highly effective catalyst for dehydrative amidation between carboxylic acids and amines. Mechanistic studies... 
BORONIC ACIDS | ROOM-TEMPERATURE | ACTIVATION | MECHANISTIC INSIGHTS | ALPHA | AMIDE BOND FORMATION | PEPTIDE-SYNTHESIS | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | DIRECT AMIDATION | ARYLBORONIC ACIDS
Journal Article
Chemical Communications : Chem Comm, ISSN 1359-7345, 01/2018, Volume 54, Issue 43, pp. 5410 - 5413
2,4-Bis(trifluoromethyl)phenylboronic acid is a highly effective catalyst for dehydrative amidation between carboxylic acids and amines. Mechanistic studies... 
Anhydrides | Boron | Amines | Catalysts | Catalysis | Carboxylic acids | Dehydration | Chemical synthesis
Journal Article
Electroanalysis, ISSN 1040-0397, 04/2018, Volume 30, Issue 4, pp. 672 - 680
This study is focused on the electrochemical detection of sialic acid (SA) using electrochemical impedance spectroscopy (EIS) and potentiometric approaches... 
Sialic Acid | Diaminobenzoic Acid | Electrodeposition | Phenylboronic Acid Modification | Sensors | ELECTROCHEMISTRY | CHEMISTRY, ANALYTICAL | POLY(ANILINE BORONIC ACID) | ANILINE | SENSOR | CANCER | FILMS | SPECTROSCOPY | POLYANILINE | POLYMER | LAYER | Electrodes | Electrochemical reactions | Usage | Raman spectroscopy | Organic acids | Electric properties
Journal Article
Science, ISSN 0036-8075, 07/2017, Volume 357, Issue 6348, pp. 283 - 286
The conversion of widely available carboxylic acids into versatile boronic esters would be highly enabling for synthesis. We found that this transformation can... 
CATALYZED DECARBONYLATIVE BORYLATION | ACTIVATION | LEWIS-BASES | MULTIDISCIPLINARY SCIENCES | ARYL HALIDES | REACTIVITY | BORONIC ESTERS | RADICALS | REDOX-ACTIVE ESTERS | BOND | ELECTRONIC-STRUCTURE | Carboxylic acids | Chemical properties | Observations | Optical properties | Photochemistry | Additives | Transformation | Phthalimide | Catalysts | Esters | Intermediates | Boron | Acids | Light | Dimers | Transformations | Functional groups
Journal Article
Organic Letters, ISSN 1523-7060, 08/2014, Volume 16, Issue 16, pp. 4256 - 4259
A bifunctional aminoboronic acid has been used to facilitate for the first time the intramolecular aza- and oxa-Michael reactions of α,β-unsaturated carboxylic... 
Combinatorial Chemistry Techniques | Stereoisomerism | Carboxylic Acids - chemistry | Coumarins - chemical synthesis | Coumarins - chemistry | Benzodioxoles - chemistry | Boronic Acids - chemistry | Molecular Structure | Catalysis | Benzodioxoles - chemical synthesis
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2008, Volume 47, Issue 26, pp. 4882 - 4886
The relay of chiral information from the α‐carbon atom of the amino acid ligand is believed to be crucial for chiral induction in the PdII‐catalyzed... 
enantioselectivity | CH activation | amino acids | boronic acids | CC coupling | C-C coupling | Amino acids | C-H activation | Enantioselectivity | Boronic acids
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 09/2010, Volume 132, Issue 38, pp. 13194 - 13196
Journal Article
Journal Article