98%
921
2 minutes
20
The shift of equilibrium by removing water with nitrile dehydrants is crucial for CeO -catalyzed synthesis of dialkyl carbonates from CO and alcohols. Two nitriles - 2-cyanopyridine and 2-furonitrile - were previously found as effective dehydrants, yet their detailed comparison as well as exploration of potential of 2-furonitrile remain insufficient. Herein, the performance of 2-cyanopyridine and 2-furonitrile was compared in the synthesis of various dialkyl carbonates. 2-furonitrile was found to be superior to 2-cyanopyridine in the synthesis of dialkyl carbonates from CO and bulky or long-chain (≥C3) alcohols. Namely, the yield of diisopropyl carbonate (up to 50 %) achieved using CeO and 2-furonitrile is comparable to or even higher than previously reported ones. Meanwhile, 2-cyanopyridine acted as a better dehydrant than 2-furonitrile in the synthesis of dimethyl carbonate and diethyl carbonate. The adsorption experiments and density functional theory calculations have indicated that the better performance of 2-furonitrile compared to 2-cyanopyridine in the synthesis of dialkyl carbonates from bulky or long-chain alcohols is due to the weaker interaction of 2-furonitrile with the CeO surface. Such weak interaction of 2-furonitrile offers a larger reaction field on the catalyst surface for both CO and alcohols.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/cssc.202300768 | DOI Listing |
J Org Chem
September 2025
Jiangsu Key Laboratory of Green Synthetic Chemistry for Functional Materials, School of Chemistry and Materials Science, Jiangsu Normal University, Xuzhou, Jiangsu 221116, PR China.
A convenient protocol for the synthesis of selenated benzoxepine derivatives via iron(III)-catalyzed 7-endo-trig cyclization has been first established via reaction of 1,7-diene containing nonactivated allyl and dialkyl diselenides under room temperature and air conditions. Research has shown that different dialkyl diselenides could react with a wide range of 1,7-diene to achieve seven-membered products in good to excellent yields. Furthermore, this synthesis was directed to obtain the desired target products, indicating that this approach has an excellent chemical selectivity.
View Article and Find Full Text PDFRSC Adv
August 2025
Natural and Medical Sciences Research Center, University of Nizwa P.O. Box 33, Postal Code 616, Birkat Al Mauz Nizwa Sultanate of Oman.
A new series of dihydronaphthalen-1(2)-one derivatives were synthesized in high yields starting from commercially available 3,5,5-trimethylcyclohex-2-en-1-one 1a, aromatic aldehydes 2, and diethyl acetylenedicarboxylate. Reaction of 1a with the aldehydes produced the respective dienones 3, which could cycloadd to dialkyl acetylenedicarboxylate, either stepwise or , under aqueous/organocatalyzed (DMAP) conditions. The respective adducts 4, were produced efficiently a Diels-Alder-double bond isomerization-oxidative aromatization sequence and were characterized based on the analysis of their H and C NMR spectra.
View Article and Find Full Text PDFEnviron Toxicol Pharmacol
September 2025
Instituto de Investigación Biosanitaria (ibs.GRANADA), Granada, Spain; Escuela Andaluza de Salud Pública (EASP), Granada, Spain; Consorcio de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Early developmental exposure to organophosphate (OP) pesticides has been linked to adverse health effects, though the underlying molecular pathways remain unclear. This study examined urinary metabolomic profiles of 387 pregnant women in their first and third trimesters using UPLC-MS/MS to identify metabolic disruptions associated with OPs exposure measured via dialkyl phosphate (DAPs) metabolites, including total, methyl and ethyl forms. Multiple linear regression models, adjusted for covariates and corrected for multiple comparisons revealed that first trimester OP exposure was significantly associated with 4-pyridoxic acid, a vitamin B6 metabolite.
View Article and Find Full Text PDFMolecules
July 2025
Functional Polymer Materials R&D and Engineering Application Technology Innovation Center of Hebei Province, Xingtai University, Xingtai 054001, China.
In the field of green chemistry, the development of more sustainable and cost-efficient methods for synthesizing primary amines is of paramount importance, with catalyst research being central to this effort. This work presents a facile, aqueous-phase synthesis of highly active cobalt catalysts (Co-Ph@SiO(x)) via pyrolysis of silica-supported cobalt-phenanthroline complexes. The optimized Co-Ph@SiO(900) catalyst achieved exceptional performance (>99% conversion, >98% selectivity) in the reductive amination of acetophenone to 1-phenylethanamine using NH/H.
View Article and Find Full Text PDFBioorg Med Chem
November 2025
Department of Chemistry, California State University Sacramento, 6000 J Street, Sacramento, CA 95819, USA. Electronic address:
Malaria, an infectious disease caused by Plasmodium parasites, continues to pose a serious global health problem. PfATP6, a calcium-transporting transmembrane protein present in Plasmodium falciparum, has been identified as a promising target for new antimalarial drugs, prompting searches for specific and potent inhibitors of this enzyme. Such compounds also have the potential of becoming novel research tools for the elucidation of the enzyme's physiological functions.
View Article and Find Full Text PDF