Results 171 to 180 of about 52,437 (280)
Gas phase flash pyrolysis of 3-azido-1,2,4-triazole: generation and ultraviolet photoelectron spectrum of N-cyanomethanimine [PDF]
I. B'Shary +4 more
openalex +1 more source
From axial and peripheral reactivity to remote derivatization, the chemical versatility of subphthalocyanines (SubPcs) renders them ideal scaffolds for the design of advanced functional materials. This review assembles the synthetic toolbox, key reaction conditions, and future challenges in SubPc functionalization, guiding the development of next ...
Marta Gómez‐Gómez +4 more
wiley +1 more source
Scedosporium-induced keratitis: insights from a case study. [PDF]
Fathima L +3 more
europepmc +1 more source
This review highlights the coordination chemistry of NHC bis‐phenolate ligands with metal centers, emphasizing structural features, redox and optical properties, and catalytic applications. Key roles in polymerization, nitrogen reduction catalysis, and small molecule activation are discussed, showcasing the versatility and potential of [OCO]M complexes
Johanna Frey +3 more
wiley +1 more source
Design, synthesis and evaluation of benzodioxole and bromofuran tethered 1,2,4-triazole hybrids as potential anti breast cancer agents with computational insights. [PDF]
R M, Hakkimane SS, B S S, Gaonkar SL.
europepmc +1 more source
This Perspective focuses on photocatalyst‐free, photoinduced modifications of biomolecules, emphasizing transformations mediated by electron donor–acceptor complexes. Mechanistic aspects, current limitations, and future opportunities are discussed, providing insight into the field of bioconjugation.
Milene Hornink +3 more
wiley +1 more source
Ultrasound-assisted green synthesis of 1,4-disubstituted 1,2,3-triazoles using natural polymer supports. [PDF]
Haseli K, Esmkhani M, Javanshir S.
europepmc +1 more source
Biologisch aktive 1,2,4-triazol-und imidazolhaltige phosphorylierte Alkohole / Biologically Active 1,2,4-Triazole and Imidazole Containing Phosphorylated Alcohols [PDF]
Ekkehard Lindner +2 more
openalex +1 more source
Why add another catalyst when the product itself holds the power to catalyze its own formation? Autocatalysis in synthetic chemistry enhances reaction efficiency and uncovers novel catalytic behavior across both closed‐shell and open‐shell systems, expanding reactivity and enabling innovative design strategies.
Jaspreet Kaur, Joshua P. Barham
wiley +1 more source

