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Mechanochemical synthesis has emerged as a powerful and more sustainable alternative to conventional solution-based methods, offering advantages such as no or only minimal solvent use, reduced reaction times, and simplified operational conditions. The integration of multiple steps into a single reaction vessel further enhances these benefits by eliminating workup and purification steps, reducing waste, and often improving overall efficiency. This review highlights recent advancements in mechanochemical one-pot multistep reactions in organic synthesis, focusing on protocols with sequential one-pot operation. Diverse transformations are covered, including heterocycle formation, functional group interconversions, and the synthesis of active pharmaceutical ingredients, while discussing both the operational and environmental advantages of these methodologies, along with their remaining challenges. Overall, mechanochemical one-pot synthesis has the potential to streamline transformations and therefore contribute to more sustainable approaches in modern organic synthetic chemistry.
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http://dx.doi.org/10.1002/chem.202500798 | DOI Listing |
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September 2025
Taikang Center for Life and Medical Sciences, Wuhan University, No.299 Bayi Road, Wuchang, Wuhan, Hubei, 430072, China.
The CRISPR-Cas12a system has emerged as a promising tool for nucleic acid-based diagnostics. However, its multi-step workflow and limited sensitivity hinder its integration into point-of-care testing (POCT). Here, the ECOT system (Engineered Cas12a for One-pot Test), a novel approach that combines protein engineering with one-pot detection, offering high sensitivity, specificity, and rapid response is introduced.
View Article and Find Full Text PDFMolecules
August 2025
International Joint Laboratory of Biomimetic and Smart Polymers, School of Materials Science and Engineering, Shanghai University, Mailbox 152, Shangda Rd. 99, Shanghai 200444, China.
Solid-liquid phase change materials (PCMs) have attracted significant attention due to their high enthalpy, which enables superior energy storage density. However, it is difficult to maintain their original shapes in a molten state. Therefore, confining PCMs within porous materials is an important method, either through mixing molten polymers and PCMs or confining PCMs in pre-prepared porous materials (e.
View Article and Find Full Text PDFBioresour Technol
August 2025
Laboratorio de Catálisis y Biocatálisis, Departamento de Química, Facultad de Ciencias, Universidad de La Serena, Raúl Bitrán 1305, La Serena, Chile. Electronic address:
The conversion of renewable biomass into value-added dicarboxylic acids, such as galactaric and glucaric acids, remains a significant challenge for the sustainable chemical industry, largely due to the lack of efficient and selective enzymatic processes. In this study, we employed protein engineering strategies to modify glucose oxidase (GOx) from Aspergillus niger, aiming to enhance its substrate specificity and broaden its oxidative capacity for the production of dicarboxylic acids. Site-saturation mutagenesis libraries targeting position F414 of the GOx-Y68W variant were constructed and screened.
View Article and Find Full Text PDFJ Org Chem
August 2025
College of Chemistry, Chemical Engineering and Resource Utilization, Northeast Forestry University, Harbin 150040, P. R. China.
Using 4-bromoindole-3-carboxylic acid derivatives (amides or esters) as substrates, this paper successfully developed a trace water-promoted, palladium-catalyzed "one-pot" reaction strategy for synthesizing 4-amino/alkoxyindole-3-carboxylic acid products. With PdCl (5 mol %) as the precatalyst, Xantphos as the ligand, and cesium pivalate as the additive, this synthetic method innovatively integrates nucleophilic substitution of amides/esters with Pd-catalyzed C-N or C-O cross-coupling into a single reaction system, achieving efficient synergy of multistep transformations. This approach facilitates a modular and rapid assembly of multisubstituted indole-3-carboxylic acids, exhibiting broad functional group compatibility while maintaining good reaction yields.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Department of Chemistry, University of Victoria, Victoria, British Columbia V8P 5C2, Canada.
Semiconducting organic nanocrystals derived from the self-assembly of conjugated polymers hold great promise for optoelectronic applications. However, fabrication of these semiconductors with high uniformity and extended dimensions remains a major challenge due to tedious multistep procedures for size control and the formidable task of attaining crystal growth oriented perpendicularly to the π-π stacking direction. Here, we present a straightforward strategy for the preparation of uniform rectangular platelet micelles with tunable size through a single-step heating-cooling-aging protocol from conjugated poly(di--hexylfluorene) (PDHF) block copolymers (BCPs).
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