Simple and efficient resolution of l,1′-bi-2-naphthol
✍ Scribed by Dongwei Cai; David L. Hughes; Thomas R. Verhoeven; Paul J. Reider
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- French
- Weight
- 255 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
Through mono-ester formation of 1,1%-bi-2-naphthol (BINOL) with pivaloyl chloride the selective mono-bromination was achieved cleanly on the other ring to afford 6-mono-bromo-1,1%-bi-2-naphthol in an efficient 86% yield.
## Cyclodextrin-assisted capillary electrophoretic resolution of 1,1'-bi-2-naphthol atropisomers Native band g-cyclodextrin (CD), neutral b-CD derivatives and ethylcarbonate derivatives of band g-CD were used as stereoselective additives for CD-capillary zone electrophoresis (CZE) resolution of at