## Abstract The ^13^C NMR spectra of methyl 2‐pyrone‐3‐, 4‐, 5‐ and 6‐carboxylates were studied and the substituent effects on the 2‐pyrone ring were compared with those of some model compounds. ^1^H NMR spectra were also recorded and discussed. The long range ^13^C, ^1^H coupling constants were ob
Carbon-13 nuclear magnetic resonance spectra: III—2-heteroadamantanes
✍ Scribed by Helmut Duddeck; Peter Wolff
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 821 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^13^C n.m.r. spectra of some 2‐heteroadamantanes and 1‐substituted 2‐heteroadamantanes are reported. The influences of the heteroatoms in the adamantane framework, and those of the substituents attached to it, on the ^13^C chemical shifts of the adamantane carbons are investigated and compared with related compounds such as the corresponding heterocyclohexane derivatives and 2‐mono‐ and 2,2‐disubstituted adamantanes. The nonadditivity of the substituent effects for 1‐substituted 2‐heteroadamantanes, especially for the geminally substituted carbons, is substantially confirmed. In addition, the influences of a missing CH~2~ group and of NCH~3~ carbons upon the ^13^C chemical shifts of the carbons in the adamantane system are described.
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