Results 171 to 180 of about 18,420 (249)

A Perspective of Soy Isoflavones on Analytical, Biological, and Chemical Attributes

Legume Science, Volume 8, Issue 3, September 2026.
ABSTRACT This review covers key aspects of soybean (Glycine max), with a particular focus on its isoflavone content and biological properties. Soybeans maintain their position as both a nutraceutical and a pharmaceutical crop, with a broad range of dietary items used worldwide, including soy milk, fermented soy products, and various dietary supplements.
Sristy Suman, Joydeep Chatterjee, Gaurav Joshi, Raj Kumar, Muhammad Wahajuddin   +4 more
wiley   +1 more source

Nano-cobalt anchored on chitosan-derived N-doped porous carbon: an efficient catalyst for α-alkylation of ketones with alcohols <i>via</i> borrowing hydrogen. [PDF]

RSC Adv
Zhang Z, Mo D, Tan Y, Chang X, Chen L, Pei X.   +5 more
europepmc   +1 more source

CEEN: A Control Software for Coupled Electrochemistry, EPR, and NMR for Redox Flow Battery and Electrosynthesis Research

Magnetic Resonance in Chemistry, Volume 64, Issue 9, Page 793-800, September 2026.
We present CEEN: a Python‐based control software for coupled electrochemistry, EPR, and NMR for redox flow battery (RFB) and electrosynthesis research. We demonstrate CEEN through practical applications relevant to aqueous organic and inorganic RFB and electrochemical synthesis research. The same setup can be readily used to study any (electrochemical)
Vince Elter, Noël de Kler, Giu A. Silva Testa, Zhiyu Zhu, Federico Paruzzo, Simon Bruderer, Evan Wenbo Zhao   +6 more
wiley   +1 more source

Total Synthesis of Antimalarial Macrolide Strasseriolide A by Ni/Zr-Mediated Reductive Ketone Coupling. [PDF]

J Org Chem
Umehara A, Kawakita KH, Sasaki M.
europepmc   +1 more source

DNA–Peptide Crosslinks Placed at Codon 249 of the p53 Tumor Suppressor Gene Induce G to A Transitions in Human Cells

ChemBioChem, Volume 27, Issue 16, 27 August 2026.
DNA‐peptide cross‐links (DpCs) are ubiquitous DNA lesions that form when cellular proteins become covalently trapped on DNA strands and are processed by proteases. DpCs are hypothesized to play a role in antitumor activity of chemotherapeutic drugs and to contribute to aging.
Priscilla Yawson, Jan Henric T. Bacurio, Honnaiah Vijay Kumar, Natalia Y. Tretyakova, Ashis K. Basu   +4 more
wiley   +1 more source

Modular Synthesis of Ru(II)-Ir(III) Complexes Bridged by a Ditopic Carbanionic NHC Ligand: Influence of Heterodinuclear Architecture on Tandem Catalysis. [PDF]

Inorg Chem
Ramos-Guzmán G, Olguín J.
europepmc   +1 more source

Noninnocent Deep Eutectic Solvents Enable Selective, Sustainable Nickel‐Catalyzed Cross‐Electrophile Couplings to Diarylmethanes

ChemSusChem, Volume 19, Issue 16, 27 August 2026.
Ni‐catalyzed cross‐electrophile coupling (XEC) of aryl iodides with benzyl chlorides proceeds efficiently in the deep eutectic solvent (DES) choline chloride/urea, replacing hazardous amide solvents. Under mild, aerobic, heterogeneous conditions, diarylmethanes form in up to 95% yield.
Andrea Nicola Paparella, Maristella Simone, Alessia Battezzato, Laura Chevet, Laetitia Chausset‐Boissarie, Muriel Durandetti, Filippo Maria Perna, Vito Capriati   +7 more
wiley   +1 more source

Lewis‐Acidic Properties and Catalytic Behavior of Hydroboration‐ and Diolysis‐Derived NHC‐Stabilized Borenium Cations

Chemistry – A European Journal, Volume 32, Issue 31, 18 August 2026.
A series of thirteen (N‐heterocyclic carbene) NHC‐stabilized borenium cations is synthesized from NHC→BH3 complexes via hydroboration and condensation with diols. The novel compounds are fully characterized. Eight crystal structures are presented. Kinetic and NMR data show how the structural features translate to catalytic activity in hydrosilylation ...
Michał Jakubczyk, Michaela Buziková, Matouš Kloda, Miroslava Litecká, Karel Škoch   +4 more
wiley   +1 more source

Oxidative Coupling of Alcohols and Amines Using Functionalized Cu(II) 2‑Quinoxolinol Salen Catalysts. [PDF]

ACS Omega
Huo X, Hicks R, Chugh A, Guragain B, Gorden JD, Gorden AEV.   +5 more
europepmc   +1 more source

Strain Release of 1‐Azabicyclo[1.1.0]butanes as a Gateway to Highly Functionalized Azetidines: New Strategies and Structural Motifs

Chemistry – A European Journal, Volume 32, Issue 31, 18 August 2026.
Over the past decade, the interest in azetidines has continuously risen, by virtue of their highly appealing pharmaceutical properties. Monocyclic, spirocyclic, and bridged azetidines can be accessed by leveraging 1‐azabicyclo[1.1.0]butanes as precursors.
Yuri Gelato, Philipp Natho, Marco Colella, Renzo Luisi   +3 more
wiley   +1 more source