Treatment of 1-diethylphosphonyl- or 1-phenylsulfonyl-2-(iodomethyl)cyclopropane-1-carboxylate with Et(3)B leads to an unsymmetrical allylated active methine radical species that gives functionalized cyclopentane derivatives with high stereoselectivity through iodine atom transfer [3 + 2] cycloaddition reaction with alkenes.
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http://dx.doi.org/10.1021/jo035771a | DOI Listing |
Inorg Chem
January 2025
Institute of Inorganic Chemistry, Czech Academy of Sciences, CZ, 250 68 Husinec-Řež, Czech Republic.
A series of -tricarbollides based on 10,11-X-7-MeN--7,8,9-CBH (X = H, Cl, Br, I) and their protonated, i.e. cationic, counterparts, which have an extra H-bridge over the B10-B11 vector in the open pentagonal belt, were prepared.
View Article and Find Full Text PDFChem Asian J
December 2024
Department State Key Laboratory of New Pharmaceutical Preparations and Excipients, College of Chemistry and Materials Science, Hebei University, Baoding, 071002, China.
Clean energy nuclear power generation is always accompanied by the release of harmful radioactive iodine. Therefore, developing efficient adsorbents has become a universal strategy to deal with this problem. Two distinct porous organic polymers (BTM-POP and DAB-POP) containing dipyridine units and benzimidazole structure were synthesized by 5,5'-([2,2'-bipyridine]-5,5'-diyl) diisophthalaldehyde with 1,2,4,5-benzenetetramine (BTM) or 3,3'-diaminobenzidine (DAB), respectively.
View Article and Find Full Text PDFJ Phys Chem A
December 2024
College of Chemistry and Materials Science, Hebei Normal University, Shijiazhuang 050024, China.
A systematic theoretical study was performed on the electrophilic and nucleophilic properties of Group 10 square-planar metal compounds [M(SCNEt)] (M = Ni , Pd , and Pt ) and their complexes. The nucleophilic metal center and coordinated sulfur atom in [M(SCNEt)] facilitate the formation of metal-involving and conventional noncovalent bonds. The presence a heavier metal center results in a more negative electrostatic potential and a larger nucleophilicity, which in turn leads to the formation of stronger metal-involving noncovalent bonds than those formed by a lighter metal center.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Institute for Organic Chemistry, University of Regensburg, 93053 Regensburg, Germany.
Diarylmethanes play, in part, a pivotal role in the design of highly potent, chiral, nonracemic drugs whose bioactivity is typically affected by the substitution pattern of their arene units. In this context, certain arenes such as -substituted benzenes or unsubstituted heteroarenes cause particular synthetic challenges, since such isosteric residues at the central methane carbon atom are typically indistinguishable for a chiral catalyst. Hence, the stereoselective incorporation of isosteric (hetero)arenes into chiral methane scaffolds requires the use of stoichiometrically differentiated building blocks, which is typically realized through preceding redox-modifying operations such as metalation or halogenation and thus associated with disadvantageous step- and redox-economic traits.
View Article and Find Full Text PDFOrg Biomol Chem
December 2024
School of Pharmacy, Guizhou Provincial Engineering Technology Research Center for Chemical Drug R&D, Guizhou Medical University, 550014 Guiyang, P. R. China.
This study presents a highly efficient method for 4-aminoquinoline derivative preparation under transition metal-free conditions. The process involves an aerobic oxidative dehydrative coupling of 2,3-dihydroquinolin-4(1)-ones with various amines, including ammonia, resulting in high yields of the desired products. The method is also applicable to substituted 4-aminoquinoline derivative construction through a cyclization/dehydrative coupling cascade process starting from 2'-amino chalcones.
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