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Alkoxy- and hydroxycarbonylations of alkenes are widely useful transformations for the preparation of esters and carboxylic acids, respectively. Catalytic systems using earth-abundant, first-row metals hold significant promise in increasing the scope and sustainability of these processes, but general methods remain virtually undeveloped. Herein, we report alkene alkoxycarbonylations and hydroxycarbonylations catalyzed by unmodified, inexpensive cobalt carbonyl under mild conditions and under low pressure promoted by light. These reactions display a broad substrate scope with respect to the alkene and alcohol components, with alkoxycarbonylations proceeding efficiently with 1 equiv of both partners, enabling coupling of complex substrates. A successful alkoxycarbonylation was performed even in the absence of solvent, displaying a remarkably low factor for the hydrocarbonylation process.
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http://dx.doi.org/10.1021/jacs.5c03769 | DOI Listing |
Biology (Basel)
July 2025
TADRUS Research Group, Department of Agricultural and Forestry Engineering, ETSIIAA, University of Valladolid, Avda. Madrid 44, 34004 Palencia, Spain.
L. is a widely used medicinal plant whose secondary metabolism and morphology are influenced by light. This study evaluated the effects of 2 and 4 h end-of-day (EOD) red/far-red (R:FR) and green (G) light on the growth, physiology, and phytochemical profile of hydroponically grown under a constant red/blue light background, compared with a red/blue control without EOD treatment.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Research Center for Materials Nanoarchitectonics, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba 305-0044, Japan.
Sustainable and chemically resilient hydrogels are critically needed in biointerface engineering, particularly for 3D cell culture systems and surface modification under physiological to mildly alkaline conditions. However, physically cross-linked cellulose nanofiber (CNF) hydrogels─despite their renewable origin and biocompatibility─typically disintegrate at pH > 8, limiting their use in polydopamine (PDA)-based surface functionalization. Here, we present a simple and scalable physical treatment strategy to fabricate alkali-resistant, physically cross-linked hydrogels from carboxymethyl cellulose nanofibers (CMCF).
View Article and Find Full Text PDFChem Pharm Bull (Tokyo)
September 2025
Peptide Research Center, Chubu University, 1200 Matsumoto-cho, Kasugai, Aichi 487-8501, Japan.
Conventional peptide synthesis involves multiple protection and deprotection steps, and typically relies on stoichiometric amounts of coupling reagents and additives. This makes the process cumbersome, and results in poor atom economy and hazardous waste generation. Therefore, direct peptide bond formation using unprotected amino acids is a promising alternative.
View Article and Find Full Text PDFJ Mol Model
September 2025
Department of Chemical Engineering, Sri Sivasubramaniya Nadar College of Engineering, Rajiv Gandhi Salai (OMR), Kalavakkam, Chennai, Tamil Nadu, 603110, India.
Context: The drug solubilization is still a significant challenge in pharmaceutical research. This study examined the sigma-surface, sigma-profile, and sigma potential of 35 water insoluble drugs using deep eutectic solvents (DES) made up of a strong hydrogen bond acceptor (HBA) choline chloride (ChCl) and several hydrogen bond donors (HBDs) at the molecular level. The combinations of ChCl and 75 HBDs include acid (C1-C10), alcohol (C1-C10), aldehyde (C1-C10), amide (C1-C10), amine (C1-C10), ester (C2-C10), ether (C2-C10), and ketone (C3-C10).
View Article and Find Full Text PDFOrg Lett
September 2025
State Key Lab of Urban Water Resource and Environment, School of Science, Harbin Institute of Technology (Shenzhen), Shenzhen 518055, China.
Iron photocatalysis has emerged as a sustainable platform for C-H functionalization. This study describes a photocatalytic strategy for the selective defluorinative functionalization of polyfluorinated aromatics. The developed methodology enables selective defluorosulfonylation with sulfur dioxide and defluorinative alkylation with alkanes under visible light irradiation.
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