A visible-light catalyzed [3 + 1 + 2] annulation for the synthesis of unsymmetrical trisubstituted amino-1,3,5-triazines from amidines, isothiocyanates, and 1,1,3,3-tetramethylguanidines has been developed. This method exhibits the advantages of easily available starting materials, insensitive to air and moisture, wide substrate scopes, high step economy, mild, metal- and ligand-free conditions, which has potential applications in the organic, medicinal, and material chemistry.
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http://dx.doi.org/10.1021/acs.joc.9b02514 | DOI Listing |
Chem Asian J
January 2025
National Institute of Technology Warangal, Department of Chemistry, Hanamkonda, 506004, Warangal, INDIA.
We report CBr4 catalyzed Michael addition of indole to α,β-unsaturated ketones for the synthesis of β-indolylketones through halogen bonding catalysis. This reaction is compatible with a diverse range of chalcones, including drug-derived chalcones containing sensitive functional groups such as amides, yielding the addition products in good yields. Additionally, 3-indolyl furanoid motifs have been synthesized through the Michael addition followed by Paal-Knorr cyclization by utilizing various unsymmetrical 1,4-enediones in a one-pot process with good yields.
View Article and Find Full Text PDFChemSusChem
January 2025
Universita degli study di cagliari, Dipartimento di Scienze Chimiche e Geologiche, Cittadella Universitaria, SS 554 bivio per Sestu, 09042, Monserrato, ITALY.
Solvent-free techniques have gained considerable attention in recent years due to their environmental advantages and potential to enable chemical reactivities beyond the reach of traditional solution-based methods. Mechanochemistry has emerged as a groundbreaking approach to drive sustainable chemical processes. Despite its promise, some challenges still need to be explored, including the overlooked issue of material leaching during grinding, a phenomenon in which components from milling media or reaction vessels, such as stainless steel, unintentionally alter reaction outcomes.
View Article and Find Full Text PDFChemistry
January 2025
East China Normal University, Shanghai Key Laboratory of Green Chemistry and Chemical Process, 3663 North Zhongshan Road, 200062, Shanghai, CHINA.
Polysulfides play an essential role across a variety of fields, including life sciences, pharmaceuticals, food science, and materials science. However, the controlled sequential installation of groups at both ends of an S-S motif poses enormous challenges due to the reversible nature of the covalent S-S bond. The application of unique disulfide reagents presents one of the most straightforward approaches for constructing diverse polysulfides.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Chemical & Material Sciences Division, CSIR-Indian Institute of Petroleum, Haridwar Road, Mohkampur, Dehradun-248005, India.
Retraction of 'Light-induced synthesis of unsymmetrical organic carbonates from alcohols, methanol and CO under ambient conditions' by Sandhya Saini , , 2021, , 12800-12803, https://doi.org/10.1039/D1CC05833A.
View Article and Find Full Text PDFBMC Chem
January 2025
The Affiliated Ganzhou Hospital, Jiangxi Medical College, Nanchang University, Ganzhou, 341000, Jiangxi, People's Republic of China.
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