## Abstract The carbon‐13 n.m.r. spectra of six substituted bisalkylamino‐__s__‐triazines are reported. The site of protonation of 2‐methoxy‐__s__‐triazines is shown to be at N‐1 or N‐3. The effect of trifluoroacetic acid on 2‐chloro‐__s__‐triazines is also discussed.
Carbon-13 n.m.r. studies of purines and 8-azapurines in basic aqueous medium
✍ Scribed by Linda Goodrich Purnell; Derek J. Hodgson
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 471 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The ^13^C n.m.r. spectra of a variety of purines and 8‐azapurines have been studied in aqueous basic medium; the shifts were measured using dioxane as reference, and corrected to the TMS scale. The compounds studied include adenine, hypoxanthine, 6‐mercaptopurine, guanine, xanthine, 8‐azaadenine, 8‐azahypoxanthine, 8‐azaguanine, 8‐azaxanthine, and 2‐thio‐8‐azaxanthine. Resonances were assigned using noise‐decoupling, selective deuteration at the 8‐position of purines, and coupled spectra. The general effect of changing from a purine to its 8‐aza analog is to produce a downfield shift of C‐2, C‐5, and C‐6 and an upfield shift of C‐4.
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