Results 121 to 130 of about 140,419 (292)
Promotion mechanism of hydroxyl groups in catalyzing CO2 cycloaddition
In this study, a series of hydroxy-functionalized quaternary ammonium salt catalysts, i.e., NEt3(HE)Br, NEt2(HE)2Br, NEt1(HE)3Br, and N(HE)4Br, were successfully prepared by quantitatively grafting hydrogen-bond donors (HBDs) as electrophilic sites on ...
Yiming Wang+5 more
doaj
Light-induced [2 + 2] cycloaddition is the most efficient way to generate cyclobutanes, while suffering from limitations of specific selectivity.
Jing-Si Wang+8 more
doaj +1 more source
A site‐selective, efficient, and mild tyrosine conjugation via tyrosinase oxidation and nucleophilic addition, allowing for site‐selective functionalization of peptides, recombinant proteins, and IgGs. Site‐selective mono‐functionalization of IgGs at Y296 enables the construction of immunoliposomes.
Hongfei Chen+13 more
wiley +1 more source
The Role of Cytochrome P450 AbyV in the Final Stages of Abyssomicin C Biosynthesis
The cytochrome P450 enzyme AbyV catalyses a key epoxidation in the final stages of the biosynthesis of the spirotetronate antibiotic abyssomicin C. Combining structural and computational data with a 13C labelling strategy was found to be a powerful approach to interrogate the biotransformation and determine the precise function of the enzyme.
Andrew J. Devine+13 more
wiley +1 more source
Stability of different phases of (C60)2 Structures [PDF]
We investigate the possible binding configurations of pairs of C60 molecules when pushed against each other. Tersoff potential, which represents intramolecular interactions well, has been used to calculate potential energies. We begin relaxation of atomic coordinates at various distances of separation and for all possible mutual orientations of the two
arxiv
Synthesis and antitumoral activity of novel biaryl hydroxy-triazole and fluorene-triazole hybrids [PDF]
Aim: The development of selective and potent antitumor agents remains a significant challenge. This study aimed to synthesize and evaluate biaryl hydroxy-1,2,3-triazoles and 9H-fluorene-1,2,3-triazole hybrids, inspired by previously identified bioactive ...
David Chafi Zeitune+6 more
doaj +1 more source
The authors introduce a high‐throughput synthesis using amide‐sulfoxonium ylides as new nucleophilic reagents, enabling a catalyst‐ and base‐free hydrocarbonation of terminal alkynes under mild conditions, resulting in various E‐alkene substituted (hetero)amide‐sulfoxonium ylides with excellent regio‐ and stereoselectivity. The late‐stage modifications
Haiting Wu+6 more
wiley +1 more source
Through the interplay of X‐ray spectroscopy and computational analysis, we show that gold +I and +III complexes, despite their physically distinct electronic structures, tend to activate substrates to similar extents. We focus in particular on the role of electron‐sharing covalency of the metal‐ligand bonds and provide an explanation for the often ...
Evgeniya A. Trifonova+5 more
wiley +1 more source
Network-analysis-guided synthesis of weisaconitine D and liljestrandinine. [PDF]
General strategies for the chemical synthesis of organic compounds, especially of architecturally complex natural products, are not easily identified. Here we present a method to establish a strategy for such syntheses, which uses network analysis.
Gallego, GM+8 more
core +2 more sources
1,3-Dipolar Cycloaddition Reaction of Thiophenecarbonitrile N-Oxides with Various Dipolarophiles [PDF]
Yoshio Iwakura+3 more
openalex +1 more source