ArticleBioorganic & medicinal chemistry letters2014
Separating the isomers--efficient synthesis of the N-hydroxysuccinimide esters of 5 and 6-carboxyfluorescein diacetate and 5 and 6-carboxyrhodamine B.
Article in Bioorganic & medicinal chemistry letters, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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3 citing papers in PubMed.
- Solid-Phase Synthesis of Fluorescent Probes for Plasma Membrane Labelling.Molecules (Basel, Switzerland) · 2021Article
- Structure-Based Design of 3-(4-Aryl-1H-1,2,3-triazol-1-yl)-Biphenyl Derivatives as P2Y14 Receptor Antagonists.Journal of medicinal chemistry · 2016Article
- Ratiometric QD-FRET Sensing of Aqueous H2S in Vitro.Analytical chemistry · 2016Article
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3 authors.
Funding
Abstract
Diacetate protection of 5 and 6-carboxyfluorescein followed by synthesis of the N-hydroxysuccinimide esters allowed ready separation of the two isomers on a multi-gram scale. The 5 and 6-carboxyrhodamine B N-hydroxysuccinimide esters were also readily synthesised and separated.
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