Results 211 to 220 of about 37,707 (289)
Characterization of Ten Novel Metabolites of a PAF Antagonist SY0916 in Rats Using LC-MS and NMR. [PDF]
He X, Zhang T, Zhao H, Ma C.
europepmc +1 more source
Heterometallic Coordination Compounds with Amino‐Acid Dithiocarbamate Ligands
This comprehensive review surveys the synthesis, molecular structures, and properties of heterobimetallic coordination compounds with amino‐acid dithiocarbamate ligands (AA‐DTCs), important O,S‐ditopic ligands. Most of the known compounds form infinite assemblies of different dimensions rather than molecular entities in the solid state.
Phil Köhler
wiley +1 more source
De novo transcriptome profiling revealing genes involved in piperine biosynthetic pathway in Piper longum L. [PDF]
Prasad M, Mathur S, Singh D, Ranjan R.
europepmc +1 more source
Exploring Bioinspired Ln3+ Complexes for Cu2+ Detection: Design and Efficacy as MRI Contrast Agents
Gd3+ complexes bearing a bioinspired Cu2+‐binding site derived from ATCUN are studied as MRI contrast agents. The presence of two amino acids (GH) is necessary to bind Cu2+ and trigger a relaxivity increase. This is due to a higher number of H2O retained close to Gd3+ through H‐bonding with Cu2+. Remarkably, the system remains selective for Cu2+ vs Zn2+
Martina Sanadar+7 more
wiley +1 more source
Structure-Activity Relationship of NMDA Receptor Ligands and Their Activities on the ERK Activation through Metabotropic Signaling Pathway. [PDF]
Kundu D+5 more
europepmc +1 more source
This review highlights recent advancements in the deconstructive transformation of unstrained cyclic amines, with a particular focus on the C−N bond cleavage of pyrrolidines. Various methodologies, including von Braun‐type, oxidative, and reductive approaches, facilitate the synthesis of diverse amines and the expansion of chemical space.
Eisuke Ota, Junichiro Yamaguchi
wiley +1 more source
Iridium-Catalyzed Stereocontrolled C(sp3)-C(sp3) Cross-Coupling of Boronic Esters and Allylic Carbonates Enabled by Boron-to-Zinc Transmetalation. [PDF]
Shen HC, Aggarwal VK.
europepmc +1 more source
The design of original disubstituted 3,4‐dihydro‐2H‐1,4‐ethano‐1,5‐naphthyridine derivatives is reported under classical and flow methodologies. The conditions are optimized and a wide range of boronic acids are used to determine the scope and limitations of Suzuki–Miyaura or Chan–Lam reactions. The design of some novel disubstituted 3,4‐dihydro‐2H‐1,4‐
Mazarine Laurent+4 more
wiley +1 more source