Synthesis and total assignment of 1H and 13C NMR spectra of new oxoisoaporphines by long-range heteronuclear correlations
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The new oxoisoaporphines 7H-dibenzo[de,h]quinolin-7-one, 5-methoxy-7H-dibenzo[de,h]quinolin-7-one, 5-methoxy-6-hydroxy-7H-dibenzo[de,h] quinolin-7-one, 5-hydroxy-7H-dibenzo[de,h]quinolin-7-one and 5-methoxy-6H-dibenzo[de,h]quinolin-6-one were prepared either by oxidation of their 2,3-dihydro derivatives or by heating (2′-(3,4-dihydro-6,7- dimethoxyisoquinolin-1′-yl)phenyl)methylbenzoate with an acetic acid/sulfuric acid mixture at 100°C. The structures were confirmed and 1H and 13C NMR spectra were completely assigned using two-dimensional NMR techniques. Copyright © 2005 John Wiley & Sons, Ltd.
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