Results 91 to 100 of about 47,847 (251)

Aza‐Büchner–Curtius–Schlotterbeck Reaction Enables Selective Construction of Quaternary Carbon Centers

open access: yesAngewandte Chemie International Edition, EarlyView.
We introduce the Aza‐Büchner–Curtius–Schlotterbeck (ABCS) reaction: A mild, catalyst‐free method for homologating aryl imines. Diverging from the traditional BCS mechanism, the diazo intermediate undergoes selective C─C insertion to form an all‐carbon quaternary center.
Simon O. Angerer   +6 more
wiley   +1 more source

Studies on 1, 2, 3-Triazole Derivatives. (1)

open access: yesYAKUGAKU ZASSHI, 1957
Shun'ichi Yamada   +2 more
openaire   +2 more sources

Activation of Metal Complexes With Ultrasound Waves for Targeted Anticancer Therapy

open access: yesAngewandte Chemie International Edition, EarlyView.
Ultrasound enables non‐invasive activation of metal‐based therapeutics deep within tumors. Acoustic cavitation can drive sonodynamic reactive oxygen species generation or mechanochemical metal–ligand bond dissociation, enabling controlled release of bioactive payloads.
Félix Grosjean   +3 more
wiley   +1 more source

Studies on 1, 2, 3-Triazole Derivatives. (3)

open access: yesYAKUGAKU ZASSHI, 1957
Shun'ichi Yamada   +2 more
openaire   +1 more source

A Ruthenium(CAAC‐5) Olefin Metathesis Catalyst for Bioconjugation

open access: yesAngewandte Chemie International Edition, EarlyView.
The aqueous instability of ruthenium catalysts restricts olefin metathesis in biological media. A Ru(CAAC‐5) complex bearing an aniline handle is reported that remains active under biologically relevant conditions and enables bioconjugation to proteins, peptides, and an artificial metalloenzyme, providing a robust platform for olefin metathesis in ...
Damian Alexander Graf   +4 more
wiley   +1 more source

Studies on 1, 2, 3-Triazole Derivatives. (2)

open access: yesYAKUGAKU ZASSHI, 1957
Shun'ichi Yamada   +2 more
openaire   +2 more sources

An Efficient Synthesis and DFT-Assisted Calculations of New 1, 2, 3-Triazole Derivatives

open access: yesJournal of Kufa for Chemical Sciences
  Under a facial 1, 3 dipolar cycloaddition reaction, three new derivatives of 1, 2, 3-triazole (5a-c) were synthesized from azides-based anilinesulfonamide derivatives (3a-c) and pentane-2, 4-dione (4) in the presence of K2CO3 as a mild catalyst.
null Hadi A. S. Jabir   +3 more
openaire   +1 more source

Spectroscopic and DFT studies of 3-(m-nitrophenyl)-4-allyl-5-mercapto-1,2,4-triazole and 3-furyl-4-allyl-5-mercapto-1,2,4-triazole

open access: yesNext Materials
In this study, the synthesized derivatives of 1,2,4-triazoles, 3-(m-nitrophenyl)-4-allyl-5-mercapto-1,2,4-triazole and 3-furyl-4-allyl-5-mercapto-1,2,4-triazole, were characterized using NMR, FTIR, Raman, and UV-Vis spectroscopies. A theoretical study of
Liana Gabrielyan   +5 more
doaj   +1 more source

A Portal‐Preorganized Cucurbit[7]uril‐Ruthenium Conjugate Enables Motif‐Selective Protein Sensing

open access: yesAngewandte Chemie International Edition, EarlyView.
Reprogramming cucurbit[7]uril (CB7) recognition through portal engineering transforms an optically silent host into a motif‐selective photoluminescent receptor. The portal‐preorganized CB7‐Rubpy conjugate directly reports changes in aromatic motif accessibility, enabling optical sensing of protein misfolding and refolding.
Patrick Gruhs   +10 more
wiley   +1 more source

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