Unusual open chain quinolinyl peroxol and its alcohol counterpart obtained through a modified Skraup-Doebner-Von Miller quinoline synthesis: Theoretical studies and complete 1H- and 13C-NMR assignments

Magnetic Resonance in Chemistry

Volumn 50, Issue 1, 2012, Pages 68-73

  Fotie, Jean ^a   Kemami Wangun, Hilaire V ^b   Dreux, Katelyn ^a   Sommerfeld, Thomas ^a   Pittman, Jacob ^a  

^a SOUTHEASTERN LOUISIANA UNIVERSITY   (United States)

^b FLORIDA ATLANTIC UNIVERSITY   (United States)

Author keywords

4 (8 ethoxy 2,3 dihydro 1H cyclopenta c quinolin 4 yl)butane 1 peroxol; 4 (8 ethoxy 2,3 dihydro 1H cyclopenta c quinolin 4 yl)butan 1 ol; ab initio calculations; density functional calculations; HMBC; HSQC; hydrogen bonds; NMR

Indexed keywords

BUTANE; CHAINS; CHEMICAL SHIFT; DENSITY FUNCTIONAL THEORY; HYDROGEN BONDS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OXIDATION; PEROXIDES;

4-(8-ETHOXY-2,3-DIHYDRO- 1H-CYCLOPENTA[C]QUINOLINE-4-YL)BUTANE-1-PEROXOL; 4-(8-ETHOXY-2,3-DIHYDRO-1H- CYCLOPENTA[C]QUINOLINE-4-YL)BUTAN-1-OL; AB INITIO CALCULATIONS; BUTAN-1-OL; DENSITY-FUNCTIONAL CALCULATIONS; HMBC; HSQC; NMR ASSIGNMENT; NMR DATA; OPEN CHAIN;

DIMERS;

EID: 84858079543     PISSN: 07491581     EISSN: 1097458X     Source Type: Journal    
DOI: 10.1002/mrc.3791     Document Type: Article

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