## 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
Chiral hydroxymethyl groups: 1H NMR assignments of the prochiral C-5′ protons of ribonucleosides
✍ Scribed by Paul C. Kline; Anthony S. Serianni
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 312 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0749-1581
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