Optically Active Seleninamides: Isolation, Absolute Configuration, and Racemization Mechanism
✍ Scribed by Nakashima, Yusuke; Shimizu, Toshio; Hirabayashi, Kazunori; Kamigata, Nobumasa
- Book ID
- 120360194
- Publisher
- American Chemical Society
- Year
- 2005
- Tongue
- English
- Weight
- 132 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0022-3263
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Thermodynamically and kinetically stabilized asymmetric diaryltelluronium imides were synthesized and optically resolved into their enantiomers on an optically active column using medium‐pressure column chromatography. The relationship between the absolute configuration and the optical
## Abstract It is shown that dimethyl 7‐isopropyl‐5, 10‐dimethylheptalene‐1, 2‐dicarboxylate (**1**) and dimethyl 5, 6, 8, 10‐tetramethylheptalene‐1, 2‐dicarboxylate (**2**) can be resolved __via__ the corresponding mono‐acids and with the aid of optically active primary or secondary amines such as