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Conformational analysis of amphetamine in solution based on unambiguous assignment of the diastereotopic benzylic protons in the 1H NMR spectra

✍ 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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✦ 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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