Results 131 to 140 of about 5,308 (247)
Cobalt‐Catalyzed C─N Bond Formation via Metal‐Hydride Hydrogen Atom Transfer (MHAT)
Cobalt‐catalyzed metal‐hydride hydrogen atom transfer (Co‐MHAT) converts simple alkenes into C─N bonds under mild, near‐neutral conditions. A shared Co─H‐initiated radical/organocobalt intermediate is channeled into radical trapping, radical‐polar crossover, or radical ligand transfer, unifying hydroamination, hydroazidation, hydroamidation, and remote
Arman Khosravi, Ming‐Yu Ngai
wiley +2 more sources
A 3D Multitask Graph Neural Network Framework for Ames Mutagenicity Prediction
Our proposed multitask graph neural network model has a high predictive accuracy for Ames mutagenicity. By operating directly on molecular graph representations instead of traditional molecular descriptors, and predicting strain‐specific results, the model outperforms most existing benchmarks.
Abigail E. Teitgen +3 more
wiley +1 more source
A Mild Disilane‐Enabled Halide‐to‐Deuterium Manifold With D2O for Aryl and Benzylic Halides
A broadly applicable Pd‐catalyzed dehalogenative deuteration enables efficient conversion of aryl and benzylic halides with inexpensive deuterium oxide (D2O). The method proceeds under exceptionally mild conditions without strong bases, harsh reductants, or stoichiometric Lewis acid halide scavengers, and tolerates a wide range of functional groups ...
Wenliang Wang +5 more
wiley +2 more sources
Lewis Acid Catalysis in the Oxidative Cycloaddition of Thiophenes1
Thiophenes 1 were treated with m-chloroperbenzoic acid (m-CPBA) under BF3·Et2O catalysis to afford thiophene S-monoxides. These could be reacted in situ as intermediary species with a number of dienophiles to provide arenes (with alkynes as dienophiles ...
Yuanqiang Li (690843) +4 more
core +1 more source
Intramolecular (4+3) Cycloadditions of Thiophenes
In contrast to the rich (4+3) cycloaddition chemistry of furans [1], only one instance of an intermolecular (4+3) cycloaddition of a thiophene has appeared with an unreported yield [2].
ZHENG, Y, Chiu, P
core
Photoswitchable Ambiphilicity: Light‐Gated Frustrated Lewis Pair Reactivity and Z‐Type Interaction
Light‐controlled ambiphilicity is realized in photoswitchable intramolecular phosphorus/boron Lewis pairs. Reversible switching modulates both the thermodynamics and kinetics of frustrated Lewis‐pair reactivity, enabling light‐gated CO2 binding and release.
Lennart Stoess +3 more
wiley +2 more sources
Sulphur speciation of PM10 samples by XANES spectroscopy
Cozzi Federico +5 more
doaj +1 more source
Regioselective C–H Activation of Substituted Thiophenes
Die C–C-Bindungsknüpfung an Thiophenen wurde mittels Pd-katalysierter C–H-Aktivierung eingehend untersucht. Unter anderem gelang die direkte C4-selektive Arylierung mono- und disubstituierter Thiophene mit Organobor-Verbindungen in hohen Ausbeuten und ...
Schnapperelle, Ingo
core
A novel C26 HBI alkane [2,6,10,13,14-pentamethyl-7-(3 -methylpentyl)pentadecane] and C26 highly branched isoprenoid (HBI) thiophenes, possessing the same carbon skeleton, have been tentatively identified in sediments of the Oligocene Menilite Formation ...
Koster, J. +5 more
core +1 more source
Gold‐Einzelatomkatalysatoren ermöglichen die selektive Shuttle‐Hydrochlorierung von Alkinen
Gold‐Einzelatomkatalysatoren auf Aktivkohle ermöglichen dank des Zusammenwirkens zwischen Au(I)‐Zentren und dem Träger die heterogene Shuttle‐Hydrochlorierung von terminalen Alkinen zu Vinylchloriden mit hoher Chemo‐ und Stereoselektivität. Das katalytische System vereint breite Substratverträglichkeit, vereinfachte Abtrennung und Wiederverwertbarkeit ...
Marc‐Eduard Usteri +8 more
wiley +1 more source

