Unique Properties of 1,5-Naphthyridin-2(1H )-one Derivatives as Environment-Polarity-Sensitive Fluorescent Dyes-Reference-Cited by-同舟云学术

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Unique Properties of 1,5-Naphthyridin-2(1H )-one Derivatives as Environment-Polarity-Sensitive Fluorescent Dyes

Published:2018-02-06 Issue:5 Volume:2018 Page:679-687
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Yokoo Hidetomo¹,Ohsaki Ayumi²^ORCID,Kagechika Hiroyuki¹^ORCID,Hirano Tomoya¹^ORCID

Affiliation:

1. Institute of Biomaterials and Bioengineering; Tokyo Medical and Dental University (TMDU); 2-3-10 Kanda-Surugadai 101-0062 Chiyoda-ku, Tokyo Japan

2. College of Humanities and Sciences; Nihon University; 3-25-40 Sakurajosui 156-8550 Setagaya-ku, Tokyo Japan

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference58 articles.

1. Signaling Recognition Events with Fluorescent Sensors and Switches

2. Design Strategies for Water-Soluble Small Molecular Chromogenic and Fluorogenic Probes

3. Macro-/micro-environment-sensitive chemosensing and biological imaging

4. Bright Ideas for Chemical Biology

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1. Synthesis of Dibenzo[b,h][1,5]naphthyridin-7(12H)-ones: The Pictet–Spengler Reaction versus a Rearrangement of 4-Phenyl[1,3]oxazolo[4,5-c]quinolines;Synthesis;2024-05-10

2. Fluorescent Probes Based on Charge and Proton Transfer for Probing Biomolecular Environment;The Chemical Record;2023-12-29

3. N-aryl-2-(trifluoromethyl)benzo[b][1,8]naphthyridin-4(1H)-one as convenient platform to design high photostable and long-lived dyad fluorophore with potential application in live-cell imaging;Journal of Photochemistry and Photobiology A: Chemistry;2023-05

4. Poly-2-aminomethyl-3-(3,4-dihydroxyphenyl)propionamide: From Structure to Proprieties;ACS Applied Polymer Materials;2023-04-10

5. D-A-D hexacatenar LCs containing bulky N-trialkoxylbenzyl carbazole caps with RGB emissions for full color palette and white LED applications;Journal of Molecular Liquids;2023-03

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