## Abstract The ^1^H NMR spectrum of naphtho [1′,2′:4,5]thieno[2,3‐__c__]quinoline is highly congested because all the protons are in an aromatic environment, and the structure of the molecule is nearly symmetric. With this in mind, the assignment of the ^1^H and ^13^C NMR spectra of this compound
Two-dimensional 1H and 13C-NMR spectra of 5-(2-dimethylaminoethoxy)-7-oxo-7H-benzo[c]fluorene, its precursor and metabolite
✍ Scribed by Antonin Lyčka; Josef Jirman; Milan Nobilis; Eva Kvasničková; Ivo M. Hais
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 266 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0749-1581
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