ArticleAngewandte Chemie (International ed. in English)2013
A common diaryl ether intermediate for the gram-scale synthesis of oxazine and xanthene fluorophores.
Article in Angewandte Chemie (International ed. in English), 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, 41 citations in OpenAlex.
- Oxidation of BINOLs by Hypervalent Iodine Reagents: Facile Synthesis of Xanthenes and Lactones.Chemistry (Weinheim an der Bergstrasse, Germany) · 2022Article
- 9-Cyanopyronin probe palette for super-multiplexed vibrational imaging.Nature communications · 2021Article
- Protocol for synthesis and use of a turn-on fluorescent probe for quantifying labile ZnSTAR protocols · 2021Article
- Silicon Substitution in Oxazine Dyes Yields Near-Infrared Azasiline Fluorophores That Absorb and Emit beyond 700 nm.Organic letters · 2018Article
- A Rationally Designed, General Strategy for Membrane Orientation of Photoinduced Electron Transfer-Based Voltage-Sensitive Dyes.ACS chemical biology · 2017Article
- Green- to far-red-emitting fluorogenic tetrazine probes - synthetic access and no-wash protein imaging inside living cells.Chemical science · 2017Article
- Study on the synthesis of the cyclopenta[f]indole core of raputindole A.Beilstein journal of organic chemistry · 2016Article
Corrections and comments
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
Abstract
Common ground: copper-catalyzed coupling reactions can be used for the high-yielding preparation of widely used oxazine and xanthene fluorophores from a common diaryl ether intermediate on a gram-scale. This general approach may facilitate the future development of novel fluorophores and probes with unique properties.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.