Preparation of a family of 10-Hydroxybenzo[h]quinoline analogues via a modified sanford reaction and their excited state intramolecular proton transfer properties

Journal of Organic Chemistry

Volumn 76, Issue 24, 2011, Pages 10220-10228

  Piechowska, Joanna ^a   Gryko, Daniel T ^a  

^a INSTITUTE OF ORGANIC CHEMISTRY   (Poland)

Author keywords

[No Author keywords available]

Indexed keywords

ACETOXYLATION; BENZO[H]QUINOLINE; CARBON-CARBON TRIPLE BONDS; ELECTRON-DONATING; ELECTRON-WITHDRAWING SUBSTITUENTS; EMISSION PROPERTIES; EXCITED-STATE INTRAMOLECULAR PROTON TRANSFER; FLUORESCENCE QUANTUM YIELD; OPTIMAL CONDITIONS; REACTION PARAMETERS; STOKES SHIFT; STRUCTURAL VARIATIONS;

ALDEHYDES; OPTIMIZATION; ORGANIC COMPOUNDS; PROTON TRANSFER; QUANTUM THEORY; QUANTUM YIELD; SYNTHESIS (CHEMICAL);

EXCITED STATES;

ACETIC ACID; ALDEHYDE; CARBON; ESTER; QUINOLINE DERIVATIVE;

ABSORPTION; ARTICLE; CATALYST; CHEMICAL BOND; CHEMICAL MODIFICATION; CHEMICAL REACTION; CHEMICAL STRUCTURE; ELECTRON TRANSPORT; EXCITED STATE INTRAMOLECULAR PROTON TRANSFER; FLUORESCENCE; HYDROLYSIS; OXIDATION; PROTON TRANSPORT; QUANTUM YIELD; REACTION TIME; SANFORD REACTION; SYNTHESIS; TEMPERATURE;

EID: 84055190976     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo202072d     Document Type: Article

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