Based on a systematic review of the usage of tartaric acid as a chiral source to resolve enantiomeric compounds, a concept is presented for synthesizing new chiral stationary phases utilizing tartaric acid derivatives as the chiral selector. The results indicate that the conformational change of one
Tartaric acid derivatives as chiral selectors in liquid chromatography
✍ Scribed by E. Heldin; K. -J. Lindner; C. Pettersson; W. Lindner; R. Rao
- Book ID
- 112733157
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 773 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0009-5893
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract A twin selector for enantioselective liquid chromatography based on __O,O__′‐bis(dimethyl)benzoyl tartaric diamide was synthesized and compared to commercially available Kromasil CHI‐DMB (__O,O__′‐bis(dimethyl)benzoyl tartaric diamide). A linear polyamide based on the same tartaric acid
## Abstract Tartaric acid‐based selectors **1** ((__R,R__)‐O,O′‐Bis(dimethylbenzoyl)‐N,N′‐diallyl‐N,N′‐dimethyl tartaramide) and **2** ((__R,R__)‐N‐allyl‐O,O′‐bis(dimethylbenzoyl) tartarimide) were synthesized, immobilized on silica, and evaluated as chiral stationary phases in enantioselective chr