Results 181 to 190 of about 2,296 (262)

Aza-Diphosphazenanes: Inorganic Cyclohexane-like Connectors with Stereochemically Tunable Exit Vectors for Molecular and Macromolecular Chemistry. [PDF]

Angew Chem Int Ed Engl
Land MA, Bedard J, George T, Masuda JD, Chitnis SS.   +4 more
europepmc   +1 more source

A Brønsted acid-base approach for the net monoselective C-F substitution of (trifluoromethyl)alkanes. [PDF]

Chem Sci
Coradi NJ, Bandar JS.
europepmc   +1 more source

Synergistic decatungstate and Brønsted acid catalysis enables direct C-H indolation of alkanes and aldehydes. [PDF]

Chem Sci
Peng G, Deng Y, Zhang M, He Y, Cheng H, Wang X, An Y, Qiu G, Zheng D.   +8 more
europepmc   +1 more source

A Three‐Dimensional Structural Model for Predicting Magnetic Exchange and Hydrogen Positions in Bis‐μ‐Hydroxido Cu(II) Dimers

European Journal of Inorganic Chemistry, Volume 29, Issue 17, 17 June 2026.
Magneto‐structural correlation in bis‐μ‐hydroxido Cu(II) dimers: The out‐of‐plane angle (α) of bridging hydroxido groups critically influences the exchange coupling constant (J). A three‐dimensional correlation combining α and the Cu‐OH‐Cu angle (θ) enables computationally accurate J prediction.
Stefani Gamboa‐Ramirez, Khalil Youssef, Rafaello Papadakis, Michel Giorgi, Sylvain Bertaina, A. Jalila Simaan, Maylis Orio   +6 more
wiley   +1 more source

Distance-Dependent, Rate-Accelerating and Diastereoselective Directing Effects in Decatungstate-Mediated Stereoediting Reactions. [PDF]

J Am Chem Soc
Liang H, Zhu J, Wang L, Wendlandt AE.
europepmc   +1 more source

Expedient Discovery of a Metallaphotoredox Cyanomethylation for Synthesizing α‐Aryl Nitriles

Chemistry – A European Journal, Volume 32, Issue 23, 16 June 2026.
A metallaphotoredox cyanomethylation reaction has been developed for the synthesis of valuable α‐aryl nitrile intermediates. The methodology was successfully applied to diverse medicinally‐relevant substrates, providing an expedient route to anti‐cancer Senexin compounds, while also removing the need for toxic cyanide reagents. The mechanism was probed
Gemma C. Cook, Blandine McKay, Craig Jamieson, Lee J. Edwards, Charlotte Harriman, Zackary S. Read, Simon T. Bate   +6 more
wiley   +1 more source

Probing the Microscopic Behavior of PFOS Clustering and Adsorption at LNAPL Interfaces; a PFOS-Water-Cyclohexane System. [PDF]

Environ Sci Technol
Sookhak Lari K, Reinhardt A, Warden AC, Rayner JL, Davis GB.   +4 more
europepmc   +1 more source

1,1‐Disubstituted Vinylbromides: Versatile Building Blocks for the Synthesis of Nitrogen‐Containing Heterocycles

European Journal of Organic Chemistry, Volume 29, Issue 23, 16 June 2026.
1,1‐Disubstituted vinylbromides are key intermediates for constructing nitrogen‐containing heterocycles. This review provides an overview of the synthetic applications of 1,1‐disubstituted vinylbromides and summarizes recent developments in reaction methodologies, mechanistic insights, and the structural diversity of N‐heterocyclic compounds accessible
Anne Westermeyer, Jun Fang, Chonghuo Liu, Guillaume Lefèvre, Gérard Guillamot, Phannarath Phansavath, Virginie Ratovelomanana‐Vidal   +6 more
wiley   +1 more source

Geminale Difunktionalisierung von Ketonen durch C–S Bindungs‐insertion photogenerierter Donor–Donor Diazoverbindungen

Angewandte Chemie, Volume 138, Issue 25, 15 June 2026.
Die geminale Difunktionalisierung leicht verfügbarer Bausteine ermöglicht einen schnellen Zugang zu molekularer Komplexität. Diese Arbeit stellt eine Strategie vor, um zwei unterschiedliche funktionelle Gruppen an einem Carbonylkohlenstoff zu installieren, indem dieser in eine Donor–Donor‐Diazo‐Verbindung überführt wird. Die Methode ist sowohl im Batch‐
Vincent George, Aryaman Pattanaik, Daniel Maddox, Lukas M. Sigmund, Giovanna Mejia, Sara Pahlén, Simon O. Angerer, Maria Schmoll, Lisa Marie Schneider, Nidhal Selmi, Mikhail Kabeshov, Giulia Bergonzini, Julia Rehbein, Burkhard König   +13 more
wiley   +1 more source

Oxidation of Cyclohexane to Cyclohexanol/Cyclohexanone Using Sol-Gel-Encapsulated Unspecific Peroxygenase from Agrocybe aegerita. [PDF]

ChemistryOpen
Wu Y, Hollmann F, Musa MM.
europepmc   +1 more source