Results 161 to 170 of about 153,572 (317)

NIR‐Activatable, Sequence‐Specific Metal‐Nucleic Acid Scaffolds for Responsive Uncaging

open access: yesAngewandte Chemie, EarlyView.
We demonstrate that long‐range nucleic acid‐mediated electron transfer can drive Pt(IV) photoreduction, establishing a new class of metal‐nucleic acid scaffolds capable of “responsive uncaging,” where hybridization with target DNA or miRNA directly triggers payload release under NIR irradiation.
Arpit Sharma   +6 more
wiley   +2 more sources

Revisiting the mechanism of the mono nuclear copper-catalyzed cycloaddition of azide and alkynes (CuAAC) by the topology of .... [PDF]

open access: yes, 2013
Comunicación presentada y aceptada en el CHITEL2013, XXXIX International Conference THEORETICAL CHEMISTS OF LATIN EXPRESSION (XXXIX Congreso Internacional de Químicos de Expresión Latina).Se analiza el mecanismo de la reacción de cicloadición, catalizada
Calvo-Losada, Saturnino   +2 more
core  

Control of Tetrazine Bioorthogonal Reactivity by Rotaxanation

open access: yesAngewandte Chemie, EarlyView.
Control of tetrazine‐mediated inverse electron demand Diels–Alder (IEDDA) reaction has been achieved by rotaxanation. Tetrazine rotaxanes were synthesized in high yield and they displayed a much slower kinetics compared to the corresponding thread. Mechanical bond disassembly upon the right stimulus activates reactivity.
Carlos Fumero‐Medina   +10 more
wiley   +2 more sources

Ligand Effects in Regio‐ and Enantioselective Cobalt‐Catalyzed Intramolecular [4+2]‐ and [2+2]‐Cycloaddition Reactions of Unactivated 1,3‐Diene‐8‐ynes and 1,3‐Diene‐8‐enes

open access: yesAngewandte Chemie, EarlyView.
Catalysts based on earth abundant cobalt {as cationic [LCoI]+} and readily available ligands are practical alternatives to prohibitively expensive Rh‐catalysts for intramolecular [4+2]‐cycloadditions of 1,3‐diene‐8‐ynes and 1,3‐diene‐8‐enes. Tunable phosphino‐oxazoline ligands enable an alternate intramolecular [2+2]‐cycloaddition mode in 1,3‐diene ...
Kiron Kumar Ghosh   +3 more
wiley   +2 more sources

Electrochemical ⍺‐C─H Functionalization of Nitramines for Accessing Bifunctional Energetic Heterocycles

open access: yesAngewandte Chemie, EarlyView.
An electrochemical α‐C─H functionalization of nitramines enables the synthesis of molecules containing bifunctional energetic heterocycles with promising properties. A telescoped, HNO3‐free sequence involving nitration and azolation steps offers a safer, modular, and scalable platform for the synthesis of energetic compounds.
Wan‐Chen Cindy Lee   +4 more
wiley   +2 more sources

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