ArticleBeilstein journal of organic chemistry2013
Efficient synthesis of phenylene-ethynylene rods and their use as rigid spacers in divalent inhibitors.
Article in Beilstein journal of organic chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Ultrafast Excited-State Dynamics of a Porphyrin-OPE Conjugate: Energy Transfer and Aggregation Effects.The journal of physical chemistry. C, Nanomaterials and interfaces · 2025Article
- A Portrait of the OPE as a Biological Agent.Molecules (Basel, Switzerland) · 2021Review
- A single-molecule electrical approach for amino acid detection and chirality recognition.Science advances · 2021Article
- Assembly of Divalent Ligands and Their Effect on Divalent Binding to Pseudomonas aeruginosa Lectin LecA.The Journal of organic chemistry · 2019Article
- Polymerization of a divalent/tetravalent metal-storing atom-mimicking dendrimer.Science advances · 2016Article
- Pseudo-Mannosylated DC-SIGN Ligands as Immunomodulants.Scientific reports · 2016Article
- Synthesis of rigid p-terphenyl-linked carbohydrate mimetics.Beilstein journal of organic chemistry · 2014Article
Corrections and comments
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Authors and funding
6 authors.
Funding
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Abstract
The synthesis of phenylene-ethynylene rods and their use as rigid spacers is described. Alternation of a Sonogashira reaction and silyl group cleavage was used to obtain rigid spacers with even and odd numbers of phenylene units. Preliminary applications of these rods in divalent systems are shown. Inhibition studies with Pseudomonas Aeruginosa lectin LecA showed that the rigid spacer proved greatly beneficial for the inhibitory potency.
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