Carbon-13 chemical shift assignments are reported for benzo [b]thiophene and l-(X-benzo[blthienyI)ethyl acetate derivatives, where X = -CH(OAc)CH, substituted at positions 2-7. Substituent chemical shift (SCS) effects for the ethyl acetate group are additive at all positions. A substantial upfield s
NMR studies of sulphur heterocycles: III—13C spectra of benzo[b]thiophene and the methylbenzo[b]thiophenes
✍ Scribed by P. D. Clark; D. F. Ewing; R. M. Scrowston
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 601 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
All carbon resonances in the title compounds have been unequivocably assigned. Steric effects in the peri substituted compounds have been compared with analogous effects in naphthalene and benzo[b]furan. The observed effects are not explained by current theory. Unusual deshielding steric shifts are observed at some carbons. Methyl substituent effects are not additive at any position in the sterically crowded 2,3‐disubstituted compounds.
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