Dinuclear phosphinidene complexes bridging two transition metal centres are now well established. However, a phosphinidene bridging a metal centre and a main group Lewis acid has not yet been reported. Herein, we describe the generation of a highly reactive phosphinidene complex bridging a tungsten and a boron centre. Furthermore, the synthesis and dyotropic rearrangement of a P-borane adduct of an -methylimidazole-stabilized neutral, electrophilic terminal phosphinidene complex is reported.
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Front Microbiol
December 2024
Department of Biological Science, Alberta Centre for Advanced Diagnostics, University of Calgary, Calgary, AB, Canada.
Introduction: Urinary tract infections (UTIs) are one of the most prevalent infections in North America and are caused by a diverse range of bacterial species. Although uropathogenesis has been studied extensively in the context of macromolecular interactions, the degree to which metabolism may contribute to infection is unclear. Currently, most of what is known about the metabolic capacity of uropathogens has been derived from genomics, genetic knockout studies or transcriptomic analyses.
View Article and Find Full Text PDFJ Biol Chem
December 2024
Division of Biological Sciences, Indian Institute of Science, Bangalore 560 012. Electronic address:
Paralogues of the bifunctional nuclease, Ribonuclease J (RNase J) demonstrate varied catalytic efficiencies despite extensive sequence and structural similarity. Of the two S. aureus RNase J paralogues, RNase J1 is substantially more active than RNase J2.
View Article and Find Full Text PDFACS Omega
December 2024
Heterogeneous Catalysis Group, Department of Chemistry, Progressive Education Society's, Modern College of Arts, Science and Commerce (Autonomous) Shivajinagar, Pune 5, Maharashtra 411005, India.
The selective deprotection of substituted aryl esters like acetates and propionates in the presence of different electron-donating and -withdrawing functional groups to the corresponding phenols in good yields was reported using the Lewis acid supported solid acid catalyst 20 InCl/MCM-41 prepared by the wet impregnation method. The textural and microscopic properties of the catalyst were studied, which revealed a high degree of dispersion of InCl over MCM-41, promising quantification of Lewis acidity, and well-ordered honeycomb structure. The methodology was further explored for the selective deprotection of acetates and propionates in the presence of substituted amides that remain unaltered.
View Article and Find Full Text PDFJ Org Chem
December 2024
State Key Laboratory of Medicinal Chemical Biology, College of Pharmacy and Tianjin Key Laboratory of Molecular Drug Research, Nankai University, Tianjin 300350, China.
Here, we demonstrated a copper(II)-catalyzed enantioselective addition of aryl amines to isatin-derived -Boc-ketimines using chiral O-N-N tridentate ligands derived from BINOL and proline. Generally, the chiral acyclic ,'-ketals were obtained in high yields (up to 98%) and excellent ee values (up to 98%). Various aryl amines could be tolerated and a gram-scale reaction was also possible.
View Article and Find Full Text PDFNat Commun
December 2024
Key Laboratory of Green Chemistry & Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu, 610064, China.
The activation of C-C bond of benzocyclobutenones under mild reaction conditions remains a challenge. We herein report a photoinduced catalyst-free regio-specific C1-C8 bond cleavage of benzocyclobutenones, enabling the generation of versatile ortho-quinoid ketene methides for aza-[4 + 2]-cycloaddition with imines, which offers a facile route to isoquinolinone derivatives, including seven family members of protoberberine alkaloids, gusanlung A, B, D, 8-oxotetrahydroplamatine, tetrahydrothalifendine, tetrahydropalmatine, and xylopinine. Furthermore, the catalytic enantioselective version of this strategy is also realized by merging synergistic photocatalysis and chiral Lewis acid catalysis.
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