𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Photochemical Reactivity and Fluorescence Analysis of 6-Methoxyquinoline, 6-Methoxyquinaldine, and 4,7-Dichloroquinoline

✍ Scribed by J. Fidanza; J. J. Aaron

Publisher
Wiley (John Wiley & Sons)
Year
2010
Volume
94
Category
Article
ISSN
0037-9646

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis, reactivity, and NMR spectrosc
Synthesis, reactivity, and NMR spectroscopy of 4,6- and 6,7-difluoro-3-methyl-1H-indazoles
✍ Carlos Pérez Medina; Concepción López; Rosa M. Claramunt; José Elguero 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 129 KB

## Abstract magnified image Four 1__H__‐indazoles, two of them doubly substituted by fluorine atoms and the other two obtained by nitration of the foregoing derivatives, were prepared and fully characterized by multinuclear NMR in solution and in solid state in view of their potential nitric oxide

Fluorescent 6-hydroxy- and 6,7-dihydroxy
Fluorescent 6-hydroxy- and 6,7-dihydroxy-4-trifluoro-methylcarbostyrils and formation of o-carboxymethylated derivatives via o-succinimide esters
✍ Georg Uray; Naresh S. Badgujar; Sona Kováčková; Wolfgang Stadlbauer 📂 Article 📅 2008 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 550 KB

## Abstract magnified image Stepwise demethylation of fluorescent 6,7‐dimethoxy‐3‐trifluoromethylcarbostyrils **5** leads to 6‐hydroxy derivatives **6** and 6,7‐dihydroxyderivative **7**. Phenolate formation shifts excitation and emission maxima from 370 and 430 nm to 430 and 480 nm for the anion

Syntheses and fluorescent properties of
Syntheses and fluorescent properties of 2-amino substituted 6,7-dimethoxy-4-(trifluoromethyl)quinolines
✍ Wolfgang Stadlbauer; Appasaheb B. Avhale; Naresh S. Badgujar; Georg Uray 📂 Article 📅 2009 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 151 KB

## Abstract magnified image 2‐Amino‐substituted 6,7‐dimethoxy‐4‐trifluoromethyl‐quinolines were synthesized from the 2‐oxo compound **1** __via__ 2‐chloroquinoline **2** and aminated with anilines or benzylamine to give highly fluorescent molecules **4**, 5. 2‐Aminoquinoline **8** was obtained __v