## Abstract Carbon‐13 NMR spectra of a variety of mono‐ and bicyclic β‐lactams have been measured and the chemical shifts of the ring carbon atoms have been assigned unambiguously. Effects of substituents on the chemical shifts of these carbons are also discussed.
Nuclear magnetic resonance III-13C NMR spectral studies on substituted indoles
✍ Scribed by K. M. Biswas; R. N. Dhara; H. Mallik; S. Roy
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 208 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^13^C signal assignments of 3‐ethyl‐1‐methylindole (1), 1‐methyl‐3‐phenylindole (3), 1,3‐dimethyl‐2‐phenylindole (5), 1‐methyl‐2,3‐diphenylindole (10), 1,5‐dimethyl‐2,3‐diphenylindole (12), 7‐methoxy‐2,3‐diphenylindole (13), 7‐methoxy‐4‐methyl‐2,3‐diphenylindole (14) and 1‐(7‐methoxy‐4‐methyl‐2,3‐diphenyl‐6‐indolyl)‐1‐(7‐methoxy‐2,3‐diphenyl‐4‐indolyl)methane (15) are reported. Contrary to an earlier report on monophenylindoles, the para carbons of the phenyl groups of 3, 5, 10 and 12–15 resonate at lower frequencies than their ortho carbons. The methoxy carbon at position 7 in 15 absorbs at a higher frequency than other similar carbons in 13–15 owing to steric inhibition to resonance.
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