Resolution of racemic 2-isobornyl-4-methylphenol into enantiomers
✍ Scribed by E. V. Buravlev; I. Yu. Chukicheva; A. V. Kutchin
- Book ID
- 106521685
- Publisher
- Springer
- Year
- 2010
- Tongue
- English
- Weight
- 153 KB
- Volume
- 59
- Category
- Article
- ISSN
- 1573-9171
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A three-step procedure for large scale preparation of pure racemic 2,3diaminobutane from relatively inexpensive meso 2,3-butanediol is described. Also, an efficient method for the resolution of (S,S) 2,3-diaminobutane from the racemic mixture in <95% ee has been developed.
## Abstract Evidence is accumulating that 7‐chloro‐4‐[4‐diethylamino‐1‐methylbutyl] amino quinoline (chloroquine) displays considerable stereoselectivity in its metabolism, pharmacokinetics, macromolecular interactions, and biological activity. The availability of the enantiomers has been hampered