Articles tagged with Stereochemistry
A team of researchers at The University of Osaka has found a novel method for creating diastereomers, which are structurally identical molecules with different biological activities. Their approach uses a group-14 allylatrane to control the reaction, resulting in the high-yield synthesis of complex molecules.
Researchers have developed a new catalysis method that can generate a diverse array of valuable compounds, including six distinct molecular scaffolds, using reprogrammed biocatalysts and sunlight-harvesting catalysts. The method opens up new possibilities for medicinal chemistry and accelerates combinatorial synthesis of novel molecules.
Researchers have discovered a way to selectively create links between sugar molecules, enabling precise control over the stereochemistry of oligosaccharides. This breakthrough could open up new avenues of biomedical research into these versatile molecules, providing access to previously difficult-to-construct oligosaccharides.
MIT chemists have developed a new way to synthesize complex oligocyclotryptamines found in plants, which could hold potential as antibiotics, analgesics, or cancer drugs. The approach allows for precise assembly of the rings and control of the 3D orientation of each component.
Researchers have developed a novel technique using a new holmium catalyst for synthesizing hydrocarbazoles with tetrasubstituted carbon. The method uses a lanthanide-based catalyst and can be recycled, paving the way for sustainable chemical processes.
Researchers from Osaka University found that (R)-ketamine can improve social impairments in mice with depression by restoring neuronal activity in the anterior insular cortex. The study suggests that (R)-ketamine may be a more effective treatment for social cognition than its counterpart (S)-ketamine.
Researchers at UC Santa Barbara have developed a synergistic method that allows for the synthesis of non-canonical amino acids, which are important for therapeutic purposes. The process shortens existing multi-step methods by 3-5 steps and provides stereoselective chemistry.
Researchers have developed a set of biocatalysts that enable precise control over free radical reactions, solving a decades-old challenge in asymmetric catalysis. The metalloenzymes can selectively convert chiral compounds into desired products, opening up new possibilities for the synthesis of bioactive molecules and everyday polymers.
Researchers at Stellenbosch University have discovered a crystalline substance that can readily give up water at temperatures as low as -70 °C. This finding has major implications for the development of materials designed to extract water from the atmosphere.
Researchers demonstrate the expanded use of a computational method called AFIR, predicting pericyclic reactions with accurate stereoselectivity based on target product molecule information. The technique successfully handles molecules up to 52 atoms and predicts stereochemistry for reactions that break Woodward-Hoffman rules.
Researchers have successfully segregated oppositely helical supramolecular polymers in a solution using audible sound, inducing surface vibrations and advection currents. This approach allows for the spatiotemporal control of chiral supramolecular systems, enabling the segregation of multiple aggregates.
Researchers developed a simplified NMR-based method to determine the atomic structure of natural products more accurately and efficiently. The new method enables chemists to analyze complex molecules with few hydrogen atoms, such as spiroepicoccin A isolated from marine microorganisms.
Researchers use computer models to predict how molecules will behave in certain reactions, controlling the emergence of specific products with desired stereochemical structures. This breakthrough enables chemists to design additives that can select the right product outcomes, revealing new insights into chemical processes.
Researchers at Virginia Tech have synthesized a biodegradable alternative to polyolefins using a new catalyst and polyester polymer. This breakthrough could lead to improved physical and chemical properties of the resulting material, making it suitable for various applications.
Chemists at Scripps Research Institute have found a way to apply the SN2 reaction to a stubborn class of chemicals, enabling the synthesis of promising antimalarial and anticancer compounds that were previously off limits. The new method uses a special acid catalyst and nitrogen-containing molecule to complete stereoinversion reactions.
Researchers at the University of Illinois have made a groundbreaking discovery in the study of enterococcal cytolysin, a 'virulence factor' that kills human cells. The enzyme responsible for its formation was found to produce distinctly different ring structures with unusual stereochemistries.
A new validated method enables accurate analysis of flavanol stereochemistry in cocoa, providing crucial insights into its cardiovascular health impact. This breakthrough addresses important gaps in knowledge and has implications for future research and development.