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Langmuir, 2021
Precise tailoring of two-dimensional nanosheets with organic molecules is critical to passivate the surface and control the reactivity, which is essential for a wide range of applications. Herein, we introduce catechols to functionalize exfoliated MXenes
James E Heckler +7 more
semanticscholar +1 more source
Precise tailoring of two-dimensional nanosheets with organic molecules is critical to passivate the surface and control the reactivity, which is essential for a wide range of applications. Herein, we introduce catechols to functionalize exfoliated MXenes
James E Heckler +7 more
semanticscholar +1 more source
Tandem conversion of lignin to catechols via demethylation and catalytic hydrogenolysis
, 2021Lignin is regarded as a potential source of various aromatic compounds and chemicals, replacing petrochemicals. Catechol and its derivatives are important platform chemicals in many industrial sectors, including agrochemicals and pharmaceuticals.
Kwang Ho Kim +6 more
semanticscholar +1 more source
ChemBioChem, 2023
AbstractThis review introduces multifaceted mutual interactions between molecules containing a catechol moiety and aggregation‐prone proteins. The complex relationships between these two molecular species have previously been elucidated primarily in a unidirectional manner, as demonstrated in cases involving the development of catechol‐based inhibitors
Nghia T. K. Le +3 more
openaire +2 more sources
AbstractThis review introduces multifaceted mutual interactions between molecules containing a catechol moiety and aggregation‐prone proteins. The complex relationships between these two molecular species have previously been elucidated primarily in a unidirectional manner, as demonstrated in cases involving the development of catechol‐based inhibitors
Nghia T. K. Le +3 more
openaire +2 more sources
Cooperativity of Catechols and Amines in High Performance Dry/Wet Adhesives.
Angewandte Chemie, 2020The outstanding adhesive performance of mussel byssal threads has been a beacon of inspiration for materials scientists over the past few decades. Historically, presence of a significant amount of the unique catecholic amino acid dihydroxyphenylalanine ...
B. D. Tiu +4 more
semanticscholar +1 more source
Reactivity of Boronic Acids toward Catechols in Aqueous Solution.
Journal of Organic Chemistry, 2020Fundamental information on the reactivities of boronic acids toward catechols in aqueous solution is required in all the fields dealing with boronic acid.
Yota Suzuki +6 more
semanticscholar +1 more source
Catechol‐Functionalized Polyolefins
Angewandte Chemie International Edition, 2020AbstractThe incorporation of comonomers during ethylene polymerization can efficiently modulate important material properties of the polyolefins. Utilizing bioresourced comonomers for the generation of high‐performance polyolefin materials is attractive from a sustainability point of view.
Yinna Na, Changle Chen
openaire +2 more sources
Journal of Steroid Biochemistry, 1988
Reaction of estrone-3,4-o-quinone with ethanethiol and glutathione leads to the formation of 4-hydroxyestrone-2-thioethers. Incubations of [1-3H]hydroxyestrone with rat liver microsomes and NADPH in the presence of glutathione results in the formation of 4-hydroxyestrone-S-glutathione with no release of tritium in the water indicating GSH addition to C-
Y J, Abul-Hajj, P L, Cisek
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Reaction of estrone-3,4-o-quinone with ethanethiol and glutathione leads to the formation of 4-hydroxyestrone-2-thioethers. Incubations of [1-3H]hydroxyestrone with rat liver microsomes and NADPH in the presence of glutathione results in the formation of 4-hydroxyestrone-S-glutathione with no release of tritium in the water indicating GSH addition to C-
Y J, Abul-Hajj, P L, Cisek
openaire +2 more sources
Journal of Steroid Biochemistry, 1981
Abstract Catechol estrogens (CEs) are a major group of active natural estrogen metabolites, formed by aromatic hydroxylation of primary estrogens at either the C-2 or C-4 position. These compounds may participate in the mechanism of estrogen action on the brain and pituitary gland.
N J, MacLusky +3 more
openaire +2 more sources
Abstract Catechol estrogens (CEs) are a major group of active natural estrogen metabolites, formed by aromatic hydroxylation of primary estrogens at either the C-2 or C-4 position. These compounds may participate in the mechanism of estrogen action on the brain and pituitary gland.
N J, MacLusky +3 more
openaire +2 more sources