2016
DOI: 10.1016/j.bmc.2016.05.022
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Bis-pyridylethenyl benzene as novel backbone for amyloid-β binding compounds

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Cited by 7 publications
(2 citation statements)
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“…All reagents and solvents were commercially purchased and used as received without further purification. Ligand 2‐bpeb was synthesized according to the previous literature methods . Elemental analyses for C, H and N were performed on a PerkinElmer 240C Elemental Analyzer at the analysis centre of Nanjing University.…”
Section: Methodsmentioning
confidence: 99%
“…All reagents and solvents were commercially purchased and used as received without further purification. Ligand 2‐bpeb was synthesized according to the previous literature methods . Elemental analyses for C, H and N were performed on a PerkinElmer 240C Elemental Analyzer at the analysis centre of Nanjing University.…”
Section: Methodsmentioning
confidence: 99%
“…Unfortunately, the safety and selectivity advantages of using NBS are counterbalanced by other issues. Specifically, light irradiation is often ineffective as an initiator for NBS [26,30], introducing the necessity to add a radical initiator, such as azobisisobutyronitrile (AIBN) [31][32][33][34] or benzoyl peroxide [35,36]; substances affected by safety concerns on transportation, storage, and use. Moreover, the regeneration of the halogen comes at a cost: the release of stoichiometric amounts of succinimide, whose recovery requires additional chemical operations, and reconversion to NBS is typically accomplished with stoichiometric Br 2 [37,38].…”
Section: Introductionmentioning
confidence: 99%