## Abstract Evidence is accumulating that 7βchloroβ4β[4βdiethylaminoβ1βmethylbutyl] amino quinoline (chloroquine) displays considerable stereoselectivity in its metabolism, pharmacokinetics, macromolecular interactions, and biological activity. The availability of the enantiomers has been hampered
β¦ LIBER β¦
Absolute configuration of the enantiomers of 7-chloro-4-[[4-(diethylamino)-1-methylbutyl]amino]quinoline (chloroquine)
β Scribed by Craig, J. Cymerman; Bhargava, Hemendra N.; Everhart, E. Thomas; LaBelle, Bruce; Ohnsorge, Ulrich; Webster, Richard V.
- Book ID
- 118165240
- Publisher
- American Chemical Society
- Year
- 1988
- Tongue
- English
- Weight
- 580 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0022-3263
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