Results 11 to 20 of about 12,942 (258)

Applications of the Reversible Boronic Acids/Boronate Switch to Nucleic Acids

open access: yesThe Chemical Record, 2022
AbstractOver the last decades, boron and nucleic acids chemistries have gained a lot of attention for biological, medicinal and analytical applications. Our laboratory has a long‐standing interest in both chemistries and owing to the ability of boronic acids to react with cis‐diol function in aqueous media we developed over the years a variety of ...
Mégane Debiais   +2 more
openaire   +2 more sources

Bioactivity of boronic acid derivative homodimers

open access: yesResults in Chemistry, 2022
Homodimers that deployed boronic acids and their esters in their termini, namely boronic acid derivative homodimers, were designed. The boronic acid pinacol ester homodimer displayed antiviral activity and the boronic acid homodimer, in contrast, exerted
Kaori Ota   +7 more
doaj   +1 more source

Photocatalytic direct borylation of carboxylic acids

open access: yesNature Communications, 2022
Boronic acids are useful reagents in organic synthesis and thus methods to prepare these compounds under mild conditions are desirable. Here, the authors synthesize boronic acids via photocatalytic decarboxylation of benzoic acids followed by borylation;
Qiang Wei   +8 more
doaj   +1 more source

Biosensors with Boronic Acid-Based Materials as the Recognition Elements and Signal Labels

open access: yesBiosensors, 2023
It is of great importance to have sensitive and accurate detection of cis-diol-containing biologically related substances because of their important functions in the research fields of metabolomics, glycomics, and proteomics.
Lin Liu   +4 more
doaj   +1 more source

A simple generic method for analyzing water sensitive pinacol boronate compounds by hydrophilic interaction liquid chromatography

open access: yesJournal of Chromatography Open, 2022
Pinacol boronates are widely used in the pharmaceutical and biomedical industries as primary building blocks for many chemical reactions, such as Suzuki coupling.
Lulu Dai, Joseph Gonzalez, Kelly Zhang
doaj   +1 more source

(4-Carbamoylphenyl)boronic acid [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2010
In the title compound, C(7)H(8)BNO(3), the mol-ecule lies on an inversion center leading to a statistical disorder of the B(OH)(2) and CONH(2) groups. In the crystal structure, mol-ecules are linked by N-H⋯O and O-H⋯O hydrogen bonds, forming sheets parallel to the bc plane.
Margarita D. Apostolova   +2 more
openaire   +3 more sources

(2,4-Dipropoxyphenyl)boronic acid [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2011
In the crystal, the title compound, C(12)H(19)BO(4), exists as a centrosymmetric O-H⋯O hydrogen-bonded dimer. Dimers are linked via C-H⋯O hydrogen bonds, generating an infinite zigzag chain oriented parallel to [1[Formula: see text]1]. The chains are assembled, giving sheets aligned parallel to (21[Formula: see text]) and inter-connected by weak C-H⋯π ...
Marek Dąbrowski   +3 more
openaire   +3 more sources

Anticancer-active 3,4-diarylthiolated maleimides synthesis via three-component radical diarylthiolation

open access: yesFrontiers in Chemistry, 2022
Herein, we report an efficient and simple copper-catalyzed oxidative diarylthiolation of maleimides with sulfur powder and aryl boronic acids, in which S powder was used as a substrate and internal oxidant.
Limei Wang   +5 more
doaj   +1 more source

Boronic Acids as Prospective Inhibitors of Metallo-β-Lactamases: Efficient Chemical Reaction in the Enzymatic Active Site Revealed by Molecular Modeling

open access: yesMolecules, 2021
Boronic acids are prospective compounds in inhibition of metallo-β-lactamases as they form covalent adducts with the catalytic hydroxide anion in the enzymatic active site upon binding.
Alexandra V. Krivitskaya   +1 more
doaj   +1 more source

Cross-Coupling Synthesis of Methylallyl Alkenes: Scope Extension and Mechanistic Study

open access: yesMolecules, 2015
Cross-coupling reactions between 2-methyl-2-propen-1-ol and various boronic acids are used to obtain aromatic-(2-methylallyl) derivatives. However, deboronation or isomerization side reactions may occur for several boronic acids.
Clémence Tabélé   +4 more
doaj   +1 more source

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