Premium
Reactions of 4‐Hydroxyquinolin‐2(1 H )‐ones with Acenaphthoquinone: Synthesis of New 1,2‐Dihydroacenaphthylene‐spiro‐tetrakis(4‐hydroxyquinolin‐2(1 H )‐ones)
Author(s) -
Aly Ashraf A.,
Ramadan Mohamed,
ElReedy Ahmed A. M.
Publication year - 2019
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.3442
Subject(s) - chemistry , triethylamine , catalysis , ethanol , nmr spectra database , spectral line , medicinal chemistry , organic chemistry , physics , astronomy
Reaction of four equivalents of 4‐hydroxyquinolin‐2(1 H )‐ones with one equivalent of acenaphthoquinone in absolute ethanol, containing catalytic triethylamine, gave 3,3′,3″,3‴‐(1,2‐dihydroacenaphthylene)‐1,1,2,2‐tetrayl‐tetrakis(4‐hydroxyquinolin‐2(1 H )‐ones) in a good to excellent yields. The structures of the products were elucidated by 1 H NMR, 13 C NMR, NMR, IR, mass spectra, and elemental analyses.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom