Results 131 to 140 of about 11,111 (220)
Bioorthogonal Reactions: Synthesis and Evaluation of Different Ligands in Copper Catalyzed Azide-Alkyne1,3-Dipolar Cycloaddition (CuAAC) [PDF]
The Copper CatalyzedAzide-Alkyne1,3-Dipolar Cycloaddition (CuAAC) reaction has unique features that qualify it to be one of the best click reactions. Its applications have been shown in different aspects and for multiple purposes.
Almansaf, Zainab Abdullah
core
A new D‐glucamine‐based triazolyl silatrane and its Fe(II)/Cu(II) complexes exhibit metal‐induced modulation of CT‐DNA binding. Experimental and theoretical investigations reveal enhanced binding affinity and conversion from groove binding to a mixed groove‐binding/intercalative interaction. ABSTRACT Research on molecular systems capable of interacting
Gurjaspreet Singh, Pawan, Brij Mohan
wiley +1 more source
Direct Mechanocatalysis and the Pursuit of Green Drug Synthesis
We place the strategy of direct mechanocatalysis, in which the milling media itself serves as the catalyst, in the context of pharmaceutical synthesis, critically assessing the current state of the art, existing limitations, and future directions for development in the field.
Maximilian Wohlgemuth +2 more
wiley +1 more source
The click‐modified targeted gadolinium nanoparticles are presented as a development of a multifunctional MRI contrast agent. The nanoplatform demonstrates improved stability and selective cellular targeting, and is expected to facilitate more precise tumor imaging while enabling further bioorthogonal conjugation for advanced cancer diagnosis and ...
Retna Putri Fauzia +10 more
wiley +1 more source
Cu(I) catalyzed, Huisgen azide/alkyne 1,3-dipolar cycloaddition (CuAAC) is recognized as the tool of choice for ligating organic molecules in a numerous fields.
Psaro, Rinaldo +3 more
core
Design and synthesis of novel 1,2,3‐triazole conjugates featuring hydroxamic acid and sulfonamide moieties: exploring dual pharmacophores for enhanced biological activity. ABSTRACT A new series of N‐hydroxy‐1‐(4‐(aryl sulfonamido)phenyl)‐1H‐1,2,3‐triazole‐4‐carboxamide derivatives (8a‐j) were synthesized through a concise multistep route integrating ...
Dineshkumar Pagar +4 more
wiley +1 more source
Not Quite Folded: Challenges in Predicting the hNPS‐hNPSR‐Ile107 Complex With AlphaFold2 Multimer
AlphaFold2 Multimer guided the design of 20 novel human neuropeptide S (hNPS) cyclic analogues. Modelling bias toward the inactive state favoured receptor blockade over activation. Exploiting a stereochemical switch in the peptide hinge region yielded four potent NPS receptor (NPSR) antagonists with pA2 up to 6.20. Lines indicate conformational bridges
Valentina Albanese +11 more
wiley +1 more source
4-Sulfanyl-1,2,3-triazole as a Powerful Ligand in CuAAC to Synthesize 1,4-Substituted 1,2,3-Triazoles Under Solvent-Free and Low Catalyst Loading. [PDF]
Shen J +8 more
europepmc +1 more source
Orthogonal Triple-Click Synthesis of Heteromimetic Triglycosylated Fullerenes. [PDF]
Nieto-Ortiz G +5 more
europepmc +1 more source
Oligonucleotides Post-Synthetic Modifications: An Overview of Clickable Nucleoside Phosphoramidites Suitable for Solid-Phase Synthesis. [PDF]
Depienne S +3 more
europepmc +1 more source

