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Formic acid (FA) and its salt are recognized as valuable molecules for various industries such as textiles and pharmaceuticals. Currently, the global demand of FA and its salts stands at 1.137 million metric tons per year, necessitating the development of sustainable methods to meet the future demands. While numerous approaches are developed for the generation of FA but the requirement of harsh reaction conditions to achieve them is unavoidable. On the other hand, the world production of biomass is estimated at 146 billion metric tons per year and that can be considered as a prospective source of FA and their salts. Additionally, cellulose accounts for approximately 35-45% of the biomass composition. Considering this, a visible-light-mediated approach is presented to produce formate directly from biomass at room temperature as well as at atmospheric pressure. In this approach, selective generation of hydroxyl radical has been achieved which later converted sugars, cellulose, and hemicellulose into formate. Furthermore, the conversion of cellulose-rich daily-life materials such as discarded paper into the product through a series of flow experiments is demonstrated. Finally, mechanistic investigations including electron paramagnetic resonance (EPR) spectroscopy, and density functional theory (DFT) calculations are conducted to gain insights into the underlying reaction mechanism.
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http://dx.doi.org/10.1002/advs.202415339 | DOI Listing |
J Am Chem Soc
September 2025
Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, P. R. China.
The direct cross-coupling of unactivated alkyl halides with aryl or heteroaryl partners remains a fundamental challenge in synthetic chemistry due to their inertness and propensity for side reactions. Herein, we report a transition-metal-free electrochemical halogen-atom transfer strategy that enables efficient alkyl radical cross-coupling via convergent paired electrolysis. In this system, anodically generated α-aminoalkyl radicals mediate the activation of alkyl iodides, while aryl/heteroaryl aldehydes or nitriles undergo cathodic reduction to afford persistent ketyl radical anions or aryl radical anions.
View Article and Find Full Text PDFJ Org Chem
September 2025
Department of Chemistry, Indian Institute of Technology Delhi, New Delhi 110016, India.
We demonstrate a direct synthesis of coumarin-3 derivatives from aryl alkynoates and hydrazines in visible light, photocatalyzed by rose bengal. The method is facile, transition-metal-free, versatile, and furnishes various 3-functionalized coumarins such as ester, acyl, aryl, carbamoyl, and sulfonyl in moderate to good yields, with the respective hydrazine reagent serving as the radical precursor. Two anti-TB molecules, and , were synthesized using this method.
View Article and Find Full Text PDFOrg Lett
September 2025
Department of Organic Chemistry, Indian Institute of Science, Bangalore 560012, India.
A transition-metal-free ring opening of bicyclo[1.1.0]butanes (BCBs) using hydroperoxides as nucleophiles in hexafluoroisopropanol (HFIP) resulting in the diastereoselective synthesis of peroxycyclobutanes under mild conditions with a broad scope is demonstrated.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Institute of Integrated Research, Institute of Science Tokyo, 4259 Nagatsuta, Midori-ku, Yokohama 226-8501, Japan.
Upgrading methane to value-added chemicals is significant but still challenging. Well-designed catalysts are required to activate methane. Extensive efforts have been dedicated to the catalytic conversion of methane over transition-metal-containing catalysts.
View Article and Find Full Text PDFJ Org Chem
September 2025
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, People's Republic of China.
We herein report the Minisci-type redox-neutral decarboxylative hydroxyalkylation of heteroarenes under photocatalyst- and transition-metal-free conditions. This methodology tolerates various functional groups that can be subsequently elaborated. Upon absorption of photons, the excited state of the α-oxocarboxylic acid forms an acyl radical, which adds to the protonated heteroarene to give the desired product after a spin center shift (SCS), reduction, and deprotonation.
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