Conformational analysis of amphetamine in solution based on unambiguous assignment of the diastereotopic benzylic protons in the 1H NMR spectra
β Scribed by Alexandros Makriyannis; James Knittel
- Publisher
- Elsevier Science
- Year
- 1981
- Tongue
- French
- Weight
- 232 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The erythro-and three-amphetamine-B-d diastereomers were synthesized and used for the unambiguous assignment of the diastereotopic benzylic protons and the measurement of vicinal l~-l~ coupling constants which were used to determine the distribution of rotamers around the central co-c8 bond in the side chain.
The conformation of a flexible drug in solution plays a role during its interaction with the receptor and may thus influence its pharmacological properties. 1,2 Amphetamine and some of its
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