109769-27-9Relevant academic research and scientific papers
New Hydroxyquinoline-Based Derivatives as Potent Modulators of Amyloid-β Aggregations
Fu, Chin-Lan,Hsu, Li-Shin,Liao, Yung-Feng,Hu, Ming-Kuan
, p. 327 - 341 (2016)
Copper and zinc have been found to contribute to the burden of amyloid-β (Aβ) aggregations in neurodegenerative Alzheimer's disease (AD). Dysregulation of these metals leads to the generation of reactive oxygen species (ROS) and eventually results in oxid
Progressive structural modification to a zinc-actuated photoinduced electron transfer (PeT) switch in the context of intracellular zinc imaging
Macias-Contreras, Miguel,Daykin, Kirsten L.,Simmons, J. Tyler,Allen, John R.,Hooper, Zachary S.,Davidson, Michael W.,Zhu, Lei
, p. 9139 - 9148 (2017)
Photoinduced electron transfer (PeT)-type fluorescent molecular switches are often applied in ion-selective sensors. Zinc-targeting sensors that contain an anilino-based electron donor (aka, the PeT 'switch') have multiple advantages over those with an al
Synthesis of substituted 3-indolylimines and indole-3-carboxaldehydes by rhodium(II)-catalyzed annulation
Rajagopal, Basker,Chou, Chih-Hung,Chung, Ching-Cheng,Lin, Po-Chiao
, p. 3752 - 3755 (2014/08/05)
An efficient Cu/Rh-catalyzed method is proposed for the synthesis of 3-indolylimines from N-propargylanilines through Rh(II)-catalyzed denitrogenative annulation of N-sulfonyl-1,2,3-triazoles. Further combined with hydrolysis or reduction, a one-pot method is developed to enable the direct incorporation of an imine, aldehyde, or amine group into an indole system from an alkyne. A variety of substituted 3-indolylimines, indole-3-carboxaldehydes, and 3-Indolylmethanamines are synthesized in good yields.
3D alkyne-azide cycloaddition: Spatiotemporally controlled by combination of aryl azide photochemistry and two-photon grafting
Li, Zhiquan,Stankevicius, Evaldas,Ajami, Aliasghar,Raciukaitis, Gediminas,Husinsky, Wolfgang,Ovsianikov, Aleksandr,Stampfl, Juergen,Liska, Robert
supporting information, p. 7635 - 7637 (2013/09/02)
A novel fluoroaryl azide with an alkyne tail was synthesized and precisely immobilized within a PEG-based matrix via two-photon induced decomposition and nitrene insertion. Well defined 3D positioning of the terminal alkyne allows site-specific micropatterning. The subsequent 3D alkyne-azide cycloaddition was realized using dye-functionalized molecules containing clickable azide moieties. The Royal Society of Chemistry.
